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Jiang W, Li L, Xia Y, Farooq S, Li G, Li S, Xu J, He S, Wu X, Huang S, Yuan J, Kong D. Neural dynamics of deception: insights from fMRI studies of brain states. Cogn Neurodyn 2025; 19:42. [PMID: 39991015 PMCID: PMC11842687 DOI: 10.1007/s11571-025-10222-4] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [Grants] [Track Full Text] [Journal Information] [Subscribe] [Scholar Register] [Received: 11/05/2024] [Revised: 01/14/2025] [Accepted: 01/16/2025] [Indexed: 02/25/2025] Open
Abstract
Deception is a complex behavior that requires greater cognitive effort than truth-telling, with brain states dynamically adapting to external stimuli and cognitive demands. Investigating these brain states provides valuable insights into the brain's temporal and spatial dynamics. In this study, we designed an experiment paradigm to efficiently simulate lying and constructed a temporal network of brain states. We applied the Louvain community clustering algorithm to identify characteristic brain states associated with lie-telling, inverse-telling, and truth-telling. Our analysis revealed six representative brain states with unique spatial characteristics. Notably, two distinct states-termed truth-preferred and lie-preferred-exhibited significant differences in fractional occupancy and average dwelling time. The truth-preferred state showed higher occupancy and dwelling time during truth-telling, while the lie-preferred state demonstrated these characteristics during lie-telling. Using the average z-score BOLD signals of these two states, we applied generalized linear models with elastic net regularization, achieving a classification accuracy of 88.46%, with a sensitivity of 92.31% and a specificity of 84.62% in distinguishing deception from truth-telling. These findings revealed representative brain states for lie-telling, inverse-telling, and truth-telling, highlighting two states specifically associated with truthful and deceptive behaviors. The spatial characteristics and dynamic attributes of these brain states indicate their potential as biomarkers of cognitive engagement in deception. Supplementary Information The online version contains supplementary material available at 10.1007/s11571-025-10222-4.
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Affiliation(s)
- Weixiong Jiang
- College of Mathematical Medicine, Zhejiang Normal University, Jinhua, Zhejiang China
- Nanbei Lake Institute for Artificial Intelligence in Medicine, Haiyan, Zhejiang China
| | - Lin Li
- College of Mathematical Medicine, Zhejiang Normal University, Jinhua, Zhejiang China
| | - Yulong Xia
- College of Mathematical Medicine, Zhejiang Normal University, Jinhua, Zhejiang China
| | - Sajid Farooq
- College of Mathematical Medicine, Zhejiang Normal University, Jinhua, Zhejiang China
| | - Gang Li
- College of Mathematical Medicine, Zhejiang Normal University, Jinhua, Zhejiang China
| | - Shuaiqi Li
- College of Mathematical Medicine, Zhejiang Normal University, Jinhua, Zhejiang China
| | - Jinhua Xu
- College of Mathematical Medicine, Zhejiang Normal University, Jinhua, Zhejiang China
| | - Sailing He
- College of Mathematical Medicine, Zhejiang Normal University, Jinhua, Zhejiang China
| | - Xiangyu Wu
- The Research Center for Children’s Literature, Zhejiang Normal University, Jinhua, Zhejiang China
| | - Shoujun Huang
- College of Mathematical Medicine, Zhejiang Normal University, Jinhua, Zhejiang China
| | - Jing Yuan
- College of Mathematical Medicine, Zhejiang Normal University, Jinhua, Zhejiang China
| | - Dexing Kong
- College of Mathematical Medicine, Zhejiang Normal University, Jinhua, Zhejiang China
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Winters DE, Spitz J, Raymond K, Natvig C, Waller R, Mikulich-Gilbertson SK, Sakai JT. Affective theory of mind impairments linked with callous-unemotional traits implicate cognitive control: A pre-registered double-blind randomized controlled trial with a dual-task paradigm. J Affect Disord 2025; 382:417-427. [PMID: 40286921 DOI: 10.1016/j.jad.2025.04.154] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Track Full Text] [Journal Information] [Submit a Manuscript] [Subscribe] [Scholar Register] [Received: 01/16/2025] [Revised: 04/04/2025] [Accepted: 04/23/2025] [Indexed: 04/29/2025]
Abstract
INTRODUCTION Youth antisocial behavior strongly associates with conduct problems (CP) and callous-unemotional (CU) traits. While CP has links to broad cognitive impairments, CU traits have specific links with cognitive control and affective theory of mind (ToM) difficulties. Evidence suggests cognitive control limitations impact affective processing in ToM amongst youth with elevated CU traits. Here we sought to improve on those initial findings by leveraging a randomized dual-task (within-trial) design to replicate and extend prior findings. METHODS In this double-blind, randomized controlled trial, 85 participants (47 % female) were stratified by sex and CU trait severity. The study employed a ToM task with cognitive, affective, and physical conditions, combined with an inhibitory processing task to tax cognitive control. Participants completed single and dual-task trials, counterbalanced to test within-subject effects. Primary hypotheses were tested with both CP and CU traits in the same model using repeated measure mixed effects to examine changes in accuracy and reaction time. RESULTS CU traits were uniquely associated with greater impairments in affective ToM under dual-task conditions, reflecting increased difficulty integrating affective information when cognitive demands were increased. CP associated with lower single ToM performance but no change during dual-task trials. Notably, participants resilient to dual-task effects reported fewer antisocial behaviors, even with elevated CU traits. LIMITATIONS While appropriately powered for study aims, the sample was underpowered to detect any potential primary and secondary variant interactions on study outcomes. CONCLUSIONS These findings support a CU trait specific cognitive-affective interaction as a mechanism critical for understanding youth antisocial behavior.
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Affiliation(s)
- Drew E Winters
- Department of Psychiatry, University of Colorado School of Medicine, Anschutz Medical Campus, Aurora, CO, USA.
| | - Juliet Spitz
- Department of Psychiatry, University of Colorado School of Medicine, Anschutz Medical Campus, Aurora, CO, USA
| | - Kristen Raymond
- Department of Psychiatry, University of Colorado School of Medicine, Anschutz Medical Campus, Aurora, CO, USA
| | - Crystal Natvig
- Department of Psychiatry, University of Colorado School of Medicine, Anschutz Medical Campus, Aurora, CO, USA
| | - Rebecca Waller
- Department of Psychology, University of Pennsylvania, Philadelphia, PA, USA
| | - Susan K Mikulich-Gilbertson
- Department of Psychiatry, University of Colorado School of Medicine, Anschutz Medical Campus, Aurora, CO, USA
| | - Joseph T Sakai
- Department of Psychiatry, University of Colorado School of Medicine, Anschutz Medical Campus, Aurora, CO, USA
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Liu P, Bai S, Li M, Zhou R. Test Anxiety and Trait Anxiety in Adolescence: Same or Different Structures? J Clin Psychol 2025; 81:583-594. [PMID: 40176481 DOI: 10.1002/jclp.23794] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Grants] [Track Full Text] [Journal Information] [Subscribe] [Scholar Register] [Received: 01/04/2024] [Revised: 10/07/2024] [Accepted: 03/18/2025] [Indexed: 04/04/2025]
Abstract
OBJECTIVES Test anxiety is positively correlated with trait anxiety. However, the precise relationship between the two is not clear. Are they two independent constructs that share a high degree of comorbidity, or the same construct manifesting in different situations (e.g., test anxiety as a special type of trait anxiety)? METHODS The present study employed two advanced analysis tools (latent profile analysis and network analysis) to evaluate the connectivity pattern between test anxiety and trait anxiety in a sample of adolescent students (N = 475, Mean age = 13.49). RESULTS The latent profile analysis revealed that all participants could be classified into three groups (low-risk, moderate-risk, and high-risk) based on their scores on two scales measuring test anxiety and trait anxiety, indicating a high degree of comorbidity between test and trait anxiety. The network analysis found that test anxiety and trait anxiety formed two relatively distinct communities, suggesting that they are two independent structures. CONCLUSIONS Together, this study provides a novel insight into the structural relationship between test anxiety and trait anxiety, indicating that while they are distinct constructs, they frequently coexist. The clinical implications for our understanding of the etiology, diagnosis and treatment of test and trait anxiety are discussed.
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Affiliation(s)
- Peibing Liu
- Department of Psychology, Nanjing University, Nanjing, China
| | - Shuliang Bai
- Department of Psychology, Nanjing University, Nanjing, China
| | - Ming Li
- Department of Psychology, Nanjing University, Nanjing, China
| | - Renlai Zhou
- Department of Psychology, Nanjing University, Nanjing, China
- Department of Radiology, Nanjing Drum Tower Hospital, the Affiliated Hospital of Nanjing University Medical School, Nanjing, China
- State Key Laboratory of Media Convergence Production Technology and Systems, Beijing, China
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Wang J, Chen J, Li J, Wu Q, Sun J, Zhang X, Li X, Yang C, Cao L, Wang J. Transdiagnostic network alterations and associated neurotransmitter signatures across major psychiatric disorders in adolescents: Evidence from edge-centric analysis of time-varying functional brain networks. J Affect Disord 2025; 380:401-412. [PMID: 40154800 DOI: 10.1016/j.jad.2025.03.151] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Track Full Text] [Journal Information] [Submit a Manuscript] [Subscribe] [Scholar Register] [Received: 12/20/2024] [Revised: 02/20/2025] [Accepted: 03/25/2025] [Indexed: 04/01/2025]
Abstract
BACKGROUND Adolescence is a pivotal phase marked by heightened vulnerability to the onset of psychiatric disorders. However, there are few transdiagnostic studies of dynamic brain networks across major psychiatric disorders during this phase. METHODS We collected resting-state functional MRI data from 189 adolescent patients (61 with bipolar disorder, 73 with major depressive disorder, and 55 with schizophrenia) and 181 healthy adolescents. Functional networks were constructed using a state-of-art edge-centric dynamic functional connectivity (DFC) approach. RESULTS Four DFC states were identified for the healthy adolescents that were related to different behavioral and cognitive terms. Disorder-related alterations were observed in two states involving motor and somatosensory processing and one state involving various cognitive functions. Regardless of the state, the three patient groups exhibited lower FC that were mainly involved in edges between different functional subsystems and were predominantly linked to regions in the somatomotor network. The patients with major depressive disorder additionally showed increased FC that were primarily linked to default mode regions. Graph-based network analysis revealed different patterns of disrupted small-world organization and altered nodal degree in the disorders in a state-dependent manner. The nodal degree alterations were correlated with the concentration of various neurotransmitters. Intriguingly, the noradrenaline concentration was engaged in the nodal degree alterations in each patient group. Finally, decreased FC involving regions in the somatomotor network showed significant correlations with clinical variables in the major depressive disorder patients. CONCLUSION These findings may help understand the developmental pathways associated with the heightened vulnerability to major psychiatric disorders during adolescence.
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Affiliation(s)
- Jing Wang
- Institute for Brain Research and Rehabilitation, South China Normal University, Guangzhou, China
| | - Jianshan Chen
- Department of Child and Adolescent Psychiatry, Affiliated Brain Hospital, Guangzhou Medical University, Guangzhou, China; Key Laboratory of Neurogenetics and Channelopathies of Guangdong Province and the Ministry of Education of China, Guangzhou Medical University, Guangzhou, China
| | - Junle Li
- Institute for Brain Research and Rehabilitation, South China Normal University, Guangzhou, China
| | - Qiuxia Wu
- Department of Child and Adolescent Psychiatry, Affiliated Brain Hospital, Guangzhou Medical University, Guangzhou, China
| | - Jiaqi Sun
- Department of Child and Adolescent Psychiatry, Affiliated Brain Hospital, Guangzhou Medical University, Guangzhou, China
| | - Xiaofei Zhang
- Department of Child and Adolescent Psychiatry, Affiliated Brain Hospital, Guangzhou Medical University, Guangzhou, China; Key Laboratory of Neurogenetics and Channelopathies of Guangdong Province and the Ministry of Education of China, Guangzhou Medical University, Guangzhou, China
| | - Xuan Li
- Department of Child and Adolescent Psychiatry, Affiliated Brain Hospital, Guangzhou Medical University, Guangzhou, China
| | - Chanjuan Yang
- Department of Child and Adolescent Psychiatry, Affiliated Brain Hospital, Guangzhou Medical University, Guangzhou, China
| | - Liping Cao
- Department of Child and Adolescent Psychiatry, Affiliated Brain Hospital, Guangzhou Medical University, Guangzhou, China; Key Laboratory of Neurogenetics and Channelopathies of Guangdong Province and the Ministry of Education of China, Guangzhou Medical University, Guangzhou, China.
| | - Jinhui Wang
- Institute for Brain Research and Rehabilitation, South China Normal University, Guangzhou, China; Key Laboratory of Brain, Cognition and Education Sciences (South China Normal University), Ministry of Education, China; Center for Studies of Psychological Application, South China Normal University, Guangzhou, China; Guangdong Key Laboratory of Mental Health and Cognitive Science, South China Normal University, Guangzhou, China; Philosophy and Social Science Laboratory of Reading and Development in Children and Adolescents (South China Normal University), Ministry of Education, China.
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Bertoli M, Zappasodi F, Croce P, De Iure D, Pettorruso M, Cavallotto C, Martinotti G, Di Matteo R, Brunetti M. Inhibitory control in Bipolar Disorder disclosed by theta band modulation. J Affect Disord 2025; 379:58-71. [PMID: 40058466 DOI: 10.1016/j.jad.2025.03.027] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Track Full Text] [Journal Information] [Submit a Manuscript] [Subscribe] [Scholar Register] [Received: 09/04/2024] [Revised: 02/11/2025] [Accepted: 03/05/2025] [Indexed: 04/12/2025]
Abstract
BACKGROUND Cognitive inhibition is key to cognitive control in healthy and psychiatric conditions. Bipolar Disorder (BD) individuals display a range of inhibitory deficits and high levels of impulsivity across all stages of the disease, including euthymia. METHODS We tested how the inhibition of heuristics in favor of analytical strategies influences the elaboration of sentences with logical quantifiers by means of a sentence-picture matching task in which the processing of quantified sentences containing the logical universal and particular quantifiers was required. Behavioral and brain oscillatory responses were assessed employing EEG recordings. RESULTS In Experiment 1, in a group of healthy volunteers, we demonstrated how the presence of a universal quantifier generates an inhibition, characterized by a high cognitive load, which is resolved at the expense of a poorer behavioral performance compared to a lower cognitive load and neutral control task. In Experiment 2, comparing healthy adults and BD patients, EEG time-frequency analysis showed a different modulation of the theta frequency band localized centrally in the medial frontal areas and representative of the different degrees of cognitive control between groups. LIMITATIONS Electrophysiological description should be interpreted with caution in light of the high signal-to-noise ratio determined by the complexity of the task. CONCLUSIONS Even in euthymia, BD limited availability of resources for cognitive inhibition impacts the functionality of a fronto-parietal cortical network, responsible for cognitive control, and orchestrated by the activity of frontal areas synchronized in theta and beta frequency.
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Affiliation(s)
- Massimo Bertoli
- Department of Neuroscience, Imaging and Clinical Sciences, University 'G. D'Annunzio' of Chieti-Pescara, Chieti, Italy.
| | - Filippo Zappasodi
- Department of Neuroscience, Imaging and Clinical Sciences, University 'G. D'Annunzio' of Chieti-Pescara, Chieti, Italy; Institute for Advanced Biomedical Technologies, University 'G. D'Annunzio' of Chieti-Pescara, Chieti, Italy
| | - Pierpaolo Croce
- Department of Neuroscience, Imaging and Clinical Sciences, University 'G. D'Annunzio' of Chieti-Pescara, Chieti, Italy; Institute for Advanced Biomedical Technologies, University 'G. D'Annunzio' of Chieti-Pescara, Chieti, Italy
| | - Danilo De Iure
- Department of Neuroscience, Imaging and Clinical Sciences, University 'G. D'Annunzio' of Chieti-Pescara, Chieti, Italy; Institute for Advanced Biomedical Technologies, University 'G. D'Annunzio' of Chieti-Pescara, Chieti, Italy
| | - Mauro Pettorruso
- Department of Neuroscience, Imaging and Clinical Sciences, University 'G. D'Annunzio' of Chieti-Pescara, Chieti, Italy; Institute for Advanced Biomedical Technologies, University 'G. D'Annunzio' of Chieti-Pescara, Chieti, Italy
| | - Clara Cavallotto
- Department of Neuroscience, Imaging and Clinical Sciences, University 'G. D'Annunzio' of Chieti-Pescara, Chieti, Italy; Institute for Advanced Biomedical Technologies, University 'G. D'Annunzio' of Chieti-Pescara, Chieti, Italy
| | - Giovanni Martinotti
- Department of Neuroscience, Imaging and Clinical Sciences, University 'G. D'Annunzio' of Chieti-Pescara, Chieti, Italy; Institute for Advanced Biomedical Technologies, University 'G. D'Annunzio' of Chieti-Pescara, Chieti, Italy
| | - Rosalia Di Matteo
- Department of Neuroscience, Imaging and Clinical Sciences, University 'G. D'Annunzio' of Chieti-Pescara, Chieti, Italy
| | - Marcella Brunetti
- Department of Neuroscience, Imaging and Clinical Sciences, University 'G. D'Annunzio' of Chieti-Pescara, Chieti, Italy; Institute for Advanced Biomedical Technologies, University 'G. D'Annunzio' of Chieti-Pescara, Chieti, Italy
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Han W, Su Y, Wang X, Yang T, Zhao G, Mao R, Zhu N, Zhou R, Wang X, Wang Y, Peng D, Wang Z, Fang Y, Chen J, Sun P. Altered resting-state brain activity in patients with major depression disorder and bipolar disorder: A regional homogeneity analysis. J Affect Disord 2025; 379:313-322. [PMID: 40081596 DOI: 10.1016/j.jad.2025.03.057] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Track Full Text] [Journal Information] [Submit a Manuscript] [Subscribe] [Scholar Register] [Received: 09/27/2024] [Revised: 03/04/2025] [Accepted: 03/10/2025] [Indexed: 03/16/2025]
Abstract
BACKGROUND Major Depressive Disorder (MDD) and Bipolar Disorder (BD) exhibit overlapping depressive symptoms, complicating their differentiation in clinical practice. Traditional neuroimaging studies have focused on specific regions of interest, but few have employed whole-brain analyses like regional homogeneity (ReHo). This study aims to differentiate MDD from BD by identifying key brain regions with abnormal ReHo and using advanced machine learning techniques to improve diagnostic accuracy. METHODS A total of 63 BD patients, 65 MDD patients, and 70 healthy controls were recruited from the Shanghai Mental Health Center. Resting-state functional MRI (rs-fMRI) was used to analyze ReHo across the brain. We applied Support Vector Machine (SVM) and SVM-Recursive Feature Elimination (SVM-RFE), a robust machine learning model known for its high precision in feature selection and classification, to identify critical brain regions that could serve as biomarkers for distinguishing BD from MDD. SVM-RFE allows for the recursive removal of non-informative features, enhancing the model's ability to accurately classify patients. Correlations between ReHo values and clinical scores were also evaluated. RESULTS ReHo analysis revealed significant differences in several brain regions. The study results revealed that, compared to healthy controls, both BD and MDD patients exhibited reduced ReHo in the superior parietal gyrus. Additionally, MDD patients showed decreased ReHo values in the Right Lenticular nucleus, putamen (PUT.R), Right Angular gyrus (ANG.R), and Left Superior occipital gyrus (SOG.L). Compared to the MDD group, BD patients exhibited increased ReHo values in the Left Inferior occipital gyrus (IOG.L). In BD patients only, the reduction in ReHo values in the right superior parietal gyrus and the right angular gyrus was positively correlated with Hamilton Depression Scale (HAMD) scores. SVM-RFE identified the IOG.L, SOG.L, and PUT.R as the most critical features, achieving an area under the curve (AUC) of 0.872, with high sensitivity and specificity in distinguishing BD from MDD. CONCLUSION This study demonstrates that BD and MDD patients exhibit distinct patterns of regional brain activity, particularly in the occipital and parietal regions. The combination of ReHo analysis and SVM-RFE provides a powerful approach for identifying potential biomarkers, with the left inferior occipital gyrus, left superior occipital gyrus, and right putamen emerging as key differentiating regions. These findings offer valuable insights for improving the diagnostic accuracy between BD and MDD, contributing to more targeted treatment strategies.
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Affiliation(s)
- Weijian Han
- Qingdao Mental Health Center, Qingdao 266034, Shandong, China
| | - Yousong Su
- Shanghai Mental Health Center, Shanghai Jiao Tong University School of Medicine, 600 South Wan Ping Road, Shanghai 200030, China
| | - Xiangwen Wang
- Qingdao Mental Health Center, Qingdao 266034, Shandong, China
| | - Tao Yang
- Shanghai Mental Health Center, Shanghai Jiao Tong University School of Medicine, 600 South Wan Ping Road, Shanghai 200030, China
| | - Guoqing Zhao
- Department of Psychology, Shandong Provincial Hospital Affiliated to Shandong First Medical University, Jinan, Shandong, China
| | - Ruizhi Mao
- Shanghai Mental Health Center, Shanghai Jiao Tong University School of Medicine, 600 South Wan Ping Road, Shanghai 200030, China
| | - Na Zhu
- Shanghai Pudong New Area Mental Health Center, Tongji University School of Medicine, Shanghai, China
| | - Rubai Zhou
- Shanghai Mental Health Center, Shanghai Jiao Tong University School of Medicine, 600 South Wan Ping Road, Shanghai 200030, China
| | - Xing Wang
- Shanghai Mental Health Center, Shanghai Jiao Tong University School of Medicine, 600 South Wan Ping Road, Shanghai 200030, China
| | - Yun Wang
- Shanghai Mental Health Center, Shanghai Jiao Tong University School of Medicine, 600 South Wan Ping Road, Shanghai 200030, China
| | - Daihui Peng
- Shanghai Mental Health Center, Shanghai Jiao Tong University School of Medicine, 600 South Wan Ping Road, Shanghai 200030, China
| | - Zuowei Wang
- Division of Mood Disorders, Shanghai Hongkou Mental Health Center, Shanghai 200083, China; Clinical Research Center for Mental Health, School of Medicine, Shanghai University, Shanghai 200083, China
| | - Yiru Fang
- Department of Psychiatry & Affective Disorders Center, Ruijin Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai 200025, China; Clinical Research Center, Shanghai Mental Health Center, Shanghai Jiao Tong University School of Medicine, Shanghai 200030, China; State Key Laboratory of Neuroscience, Shanghai Institue for Biological Sciences, CAS, Shanghai 200031, China; Shanghai Key Laboratory of Psychotic Disorders, Shanghai 201108, China
| | - Jun Chen
- Shanghai Mental Health Center, Shanghai Jiao Tong University School of Medicine, 600 South Wan Ping Road, Shanghai 200030, China.
| | - Ping Sun
- Qingdao Mental Health Center, Qingdao 266034, Shandong, China.
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Liang S, Gao Y, Palaniyappan L, Song XM, Zhang T, Han JF, Tan ZL, Li T. Transcriptional substrates of cortical thickness alterations in anhedonia of major depressive disorder. J Affect Disord 2025; 379:118-126. [PMID: 40044088 DOI: 10.1016/j.jad.2025.03.003] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Track Full Text] [Journal Information] [Submit a Manuscript] [Subscribe] [Scholar Register] [Received: 08/12/2024] [Revised: 02/26/2025] [Accepted: 03/01/2025] [Indexed: 03/14/2025]
Abstract
BACKGROUND Anhedonia is a core symptom of major depressive disorder (MDD), which has been shown to be associated with abnormalities in cortical morphology. However, the correlation between cortical thickness (CT) changes with anhedonia in MDD and gene expression remains unclear. METHODS We investigated the link between brain-wide gene expression and CT correlates of anhedonia in individuals with MDD, using 7 Tesla neuroimaging and a publicly available transcriptomic dataset. The interest-activity score was used to evaluation MDD with high anhedonia (HA) and low anhedonia (LA). Nineteen patients with HA, nineteen patients with LA, and twenty healthy controls (HC) were enrolled. We investigated CT alterations of anhedonia subgroups relative to HC and related cortical gene expression, enrichment and specific cell types. We further used Neurosynth and von Economo-Koskinas atlas to assess the meta-analytic cognitive functions and cytoarchitectural variation associated with anhedonia-related cortical changes. RESULTS Both patient subgroups exhibited widespread CT reduction, with HA manifesting more pronounced changes. Gene expression related to anhedonia had significant spatial correlations with CT differences. Transcriptional signatures related to anhedonia-associated cortical thinning were connected to mitochondrial dysfunction and enriched in adipogenesis, oxidative phosphorylation, mTORC1 signaling pathways, involving neurons, astrocytes, and oligodendrocytes. These CT alterations were significantly correlated with meta-analytic terms involving somatosensory processing and pain perception. HA had reduced CT within the somatomotor and ventral attention networks, and in agranular cortical regions. LIMITATIONS These include measuring anhedonia using interest-activity score and employing a cross-sectional design. CONCLUSIONS This study sheds light on the molecular basis underlying gene expression associated with anhedonia in MDD, suggesting directions for targeted therapeutic interventions.
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Affiliation(s)
- Sugai Liang
- Affiliated Mental Health Center & Hangzhou Seventh People's Hospital, School of Medicine, Zhejiang University, Hangzhou 310013, China
| | - Yuan Gao
- Affiliated Mental Health Center & Hangzhou Seventh People's Hospital, School of Medicine, Zhejiang University, Hangzhou 310013, China; Interdisciplinary Institute of Neuroscience and Technology, School of Medicine, Zhejiang University, Hangzhou 310027, China
| | - Lena Palaniyappan
- Douglas Mental Health University Institute, Department of Psychiatry, McGill University, Montreal, Quebec H4H1R3, Canada.; Department of Psychiatry, Schulich School of Medicine and Dentistry, Western University, London, Ontario N6A5C1, Canada; Robarts Research Institute, Schulich School of Medicine and Dentistry, Western University, London, Ontario N6A5K8, Canada
| | - Xue-Mei Song
- Affiliated Mental Health Center & Hangzhou Seventh People's Hospital, School of Medicine, Zhejiang University, Hangzhou 310013, China; Interdisciplinary Institute of Neuroscience and Technology, School of Medicine, Zhejiang University, Hangzhou 310027, China
| | - Tian Zhang
- Affiliated Mental Health Center & Hangzhou Seventh People's Hospital, School of Medicine, Zhejiang University, Hangzhou 310013, China
| | - Jin-Fang Han
- Affiliated Mental Health Center & Hangzhou Seventh People's Hospital, School of Medicine, Zhejiang University, Hangzhou 310013, China
| | - Zhong-Lin Tan
- Affiliated Mental Health Center & Hangzhou Seventh People's Hospital, School of Medicine, Zhejiang University, Hangzhou 310013, China.
| | - Tao Li
- Affiliated Mental Health Center & Hangzhou Seventh People's Hospital, School of Medicine, Zhejiang University, Hangzhou 310013, China; Liangzhu Laboratory, MOE Frontier Science Center for Brain Science and Brain-machine Integration, State Key Laboratory of Brain-machine Intelligence, Zhejiang University, Hangzhou 310000, China; NHC and CAMS Key Laboratory of Medical Neurobiology, Zhejiang University, Hangzhou 310063, China.
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8
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Lin SM, Han Y, Hu JY, Wang XY, Zeng YM, Wei H, Shao Y, Yu Y. Resting-state functional brain networks in hypertensive retinopathy. Brain Res Bull 2025; 226:111350. [PMID: 40250734 DOI: 10.1016/j.brainresbull.2025.111350] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Track Full Text] [Journal Information] [Subscribe] [Scholar Register] [Received: 12/11/2024] [Revised: 04/13/2025] [Accepted: 04/15/2025] [Indexed: 04/20/2025]
Abstract
OBJECTIVE Hypertensive retinopathy (HR) is known to have effects on the brain's function. This neuroimaging investigation aimed to evaluate alterations in functional network connectivity and the topological properties of brain networks in in patients with HR. METHODS The study involved twenty patients with HR and forty-one healthy controls (HC), all of whom underwent resting-state functional MRI scans. Independent component analysis and graph theory analysis were calculated to identify functional connectivity and topological property abnormalities between the two groups. RESULTS Compared to HC, patients with HR demonstrated increased internetwork functional connectivity. Furthermore, these patients showed increased intranetwork functional connectivity within the right precuneus of the default mode network. Graph theory analysis revealed that both groups demonstrated a small-world topology. However, significant differences were observed in global and regional network metrics in HR patients compared to HC. CONCLUSION These findings highlight the alterations in functional connectivity and topological properties of brain networks in patients with HR, offering valuable insights into the potential neural mechanisms underlying their condition.
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Affiliation(s)
- Si-Min Lin
- Department of Radiology, Xiamen Cardiovascular Hospital of Xiamen University, School of Medicine, Fujian Branch of National Clinical Research Center for Cardiovascular Diseases, Xiamen, Fujian, China
| | - Yi Han
- Department of Ophthalmology, The First Affiliated Hospital of University of South China, Hengyang Medical School, University of South China, Hengyang, Hunan, China
| | - Jin-Yu Hu
- Department of Ophthalmology, The First Affiliated Hospital, Jiangxi Medical College, Nanchang University, Nanchang, Jiangxi, China
| | - Xiao-Yu Wang
- Department of Ophthalmology, The First Affiliated Hospital, Jiangxi Medical College, Nanchang University, Nanchang, Jiangxi, China
| | - Yan-Mei Zeng
- Department of Ophthalmology, The First Affiliated Hospital, Jiangxi Medical College, Nanchang University, Nanchang, Jiangxi, China
| | - Hong Wei
- Department of Ophthalmology, The First Affiliated Hospital, Jiangxi Medical College, Nanchang University, Nanchang, Jiangxi, China
| | - Yi Shao
- Department of Ophthalmology, The First Affiliated Hospital, Jiangxi Medical College, Nanchang University, Nanchang, Jiangxi, China; Department of Ophthalmology, Shanghai General Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China.
| | - Yao Yu
- Department of Endocrine and Metabolic, The First Affiliated Hospital, Jiangxi, Medical College, Nanchang University, Jiangxi Clinical Research Center for Endocrine and Metabolic Disease, Jiangxi Branch of National Clinical Research Center for Metabolic Disease, Nanchang, Jiangxi, China.
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Ümmü E, Kurt E, Bayram A. Alterations within and between intrinsic connectivity networks in cognitive interference resolution. Int J Psychophysiol 2025; 212:112577. [PMID: 40306372 DOI: 10.1016/j.ijpsycho.2025.112577] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Track Full Text] [Journal Information] [Subscribe] [Scholar Register] [Received: 08/28/2024] [Revised: 04/22/2025] [Accepted: 04/24/2025] [Indexed: 05/02/2025]
Abstract
Cognitive interference resolution (CIR) is the process of maintaining goal-directed focus despite the presence of distractions. While CIR has been extensively studied through localized activation analyses, its network-level dynamics remain underexplored with sufficient methodological diversity. In this study, we investigated the task-modulated intrinsic connectivity networks (ICNs) and their dynamic interactions with detailed subnetwork segmentation during CIR using fMRI data from 27 healthy adults performing the Multi-Source Interference Task (MSIT). We applied high-order group independent component analysis (ICA) to extract ICN subcomponents, followed by task-modulated component identification and dynamic functional connectivity analysis to examine network interactions. Our results reveal that the dorsal attention network (DAN) and cognitive control network (CCN) show increased activation and connectivity, while the default mode network (DMN) and limbic network exhibit decreased activation and connectivity. Additionally, the visual and cerebellum networks emerge as key intermediaries in CIR, as DAN and CCN strengthen their connectivity with these networks rather than directly interacting with each other. Furthermore, network reconfiguration patterns suggest functional segregation within the somatomotor network and CCN, indicating specialized subcomponent contributions. These findings provide a granular understanding of ICN activations and dynamic inter-network communication during CIR, offering new insights into the flexible reorganization of brain networks in response to cognitive interference.
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Affiliation(s)
- Eylem Ümmü
- Graduate School of Health Sciences, Istanbul University, Istanbul 34126, Türkiye; Department of Neuroscience, Aziz Sancar Institute of Experimental Medicine, Istanbul University, Istanbul 34093, Türkiye; Hulusi Behçet Life Sciences Research Laboratory, Neuroimaging Unit, Istanbul University, Istanbul 34093, Türkiye.
| | - Elif Kurt
- Department of Neuroscience, Aziz Sancar Institute of Experimental Medicine, Istanbul University, Istanbul 34093, Türkiye; Hulusi Behçet Life Sciences Research Laboratory, Neuroimaging Unit, Istanbul University, Istanbul 34093, Türkiye
| | - Ali Bayram
- Department of Neuroscience, Aziz Sancar Institute of Experimental Medicine, Istanbul University, Istanbul 34093, Türkiye; Hulusi Behçet Life Sciences Research Laboratory, Neuroimaging Unit, Istanbul University, Istanbul 34093, Türkiye
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10
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Menabò L, Skrzypiec G, Slee P, Guarini A. What roles matter? An explorative study on bullying and cyberbullying by using the eye-tracker. BRITISH JOURNAL OF EDUCATIONAL PSYCHOLOGY 2025; 95:249-269. [PMID: 37186299 PMCID: PMC12068039 DOI: 10.1111/bjep.12604] [Citation(s) in RCA: 3] [Impact Index Per Article: 3.0] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Track Full Text] [Download PDF] [Figures] [Journal Information] [Subscribe] [Scholar Register] [Received: 09/08/2022] [Revised: 03/10/2023] [Accepted: 04/17/2023] [Indexed: 05/17/2023]
Abstract
BACKGROUND Bullying and cyberbullying are serious public health concerns that involve more roles beyond the bully and the victim (pro-bullies, defenders, bystanders). However, students often perceive the phenomena as dyadic. AIM The purpose was to examine students' perceptions of different roles when observing bullying and cyberbullying scenes combining implicit (attention by using the eye-tracker) and explicit (verbal reports) measures. SAMPLE We included 50 Italian students (aged 10-11). METHODS Students watched 12 drawings of different types of bullying and cyberbullying while their gaze was tracked, and subsequently described each drawing verbally. We ran repeated measure ANOVAs to compare attentional indexes (fixation count, visit count and total fixation duration) in observing roles and Cochran's Q test to evaluate differences in the verbal identification of roles. RESULTS Overall, the victim and bully were the most observed and identified roles in every type of bullying and cyberbullying scenario. Concerning the other roles, a discrepancy was observed between the implicit and explicit measures since although it was greatly identified, the pro-bully received less attention, and while the bystander received great attention, it was mentioned less. Finally, the defender was more observed and identified in physical bullying and cyberbullying. CONCLUSIONS Our study points out for the first time the dyadic perception of the phenomena among adolescents using implicit and explicit measures and sheds light on differences among the roles in different forms of bullying. Further research including the eye-tracker would be worthwhile given the possibility of exploring the phenomena from different perspectives.
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Affiliation(s)
- Laura Menabò
- Department of Psychology “Renzo Canestrari”University of BolognaBolognaItaly
| | - Grace Skrzypiec
- Department of EducationFlinders UniversityAdelaideSouth AustraliaAustralia
| | - Phillip Slee
- Department of EducationFlinders UniversityAdelaideSouth AustraliaAustralia
| | - Annalisa Guarini
- Department of Psychology “Renzo Canestrari”University of BolognaBolognaItaly
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11
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Hu Y, Zeng Y, Fu T, Hong D, Yang H, Zhu Z, Cheng D, Dang C, Song Y, Yang C, Yin W, Zhou Y. Functional connectivity anomalies in medication-naive children with ADHD: Diagnostic potential, symptoms interpretation, and a mediation model. Clin Neurophysiol 2025; 174:212-219. [PMID: 40305882 DOI: 10.1016/j.clinph.2025.04.011] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Track Full Text] [Journal Information] [Subscribe] [Scholar Register] [Received: 08/06/2024] [Revised: 03/24/2025] [Accepted: 04/08/2025] [Indexed: 05/02/2025]
Abstract
OBJECTIVE To identify reliable electroencephalography (EEG) biomarkers for attention deficit/hyperactivity disorder (ADHD) by investigating anomalous functional connectivity patterns and their clinical relevance. METHODS Resting-state EEG data were collected from 74 children aged 6-12 (33 unmedicated ADHD; 41 typically developing). Functional connectivity was quantified using the imaginary part of coherency (ICOH). Machine learning (ML)-based support vector machine (SVM) modeling, regression, and mediation analyses linked connectivity features to symptom severity and diagnostic classification. RESULTS Children with ADHD exhibited beta (β) band hypo-connectivity in frontal regions (Fp2-F4, Fp1-Cz, F7-Cz) and theta (θ) band hyper-connectivity in left parietal-central networks (C3-P7, P3-P7, etc.). An SVM classifier achieved an average area under the curve of 0.89 using three connectivity features. Left parietal θ band hyper-connectivity (C3-P7) correlated with both inattention and hyperactivity/impulsivity and mediated their interrelationship. CONCLUSIONS ADHD is characterized by disrupted frontoparietal connectivity, with θ band hyper-connectivity in sensory-integration networks potentially compensating for impaired frontal regulation. SIGNIFICANCE These findings highlight C3-P7 θ band connectivity as both a diagnostic and mechanistic biomarker, providing novel target for neurofeedback therapies and enhancing the differential diagnosis in neurodevelopmental disorders.
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Affiliation(s)
- Yingzi Hu
- The Affiliated Brain Hospital, Guangzhou Medical University, Guangzhou 510370, China; Key Laboratory of Neurogenetics and Channelopathies of Guangdong Province and the Ministry of Education of China, Guangzhou Medical University, Guangzhou 510370, China; Institute of Psychiatry and Psychology, The Affiliated Brain Hospital, Guangzhou Medical University, Guangzhou 510370, China.
| | - Yexian Zeng
- The Affiliated Brain Hospital, Guangzhou Medical University, Guangzhou 510370, China; Key Laboratory of Neurogenetics and Channelopathies of Guangdong Province and the Ministry of Education of China, Guangzhou Medical University, Guangzhou 510370, China; Institute of Psychiatry and Psychology, The Affiliated Brain Hospital, Guangzhou Medical University, Guangzhou 510370, China.
| | - Tong Fu
- The Affiliated Brain Hospital, Guangzhou Medical University, Guangzhou 510370, China; Institute of Psychiatry and Psychology, The Affiliated Brain Hospital, Guangzhou Medical University, Guangzhou 510370, China; Shanghai Mental Health Center, Shanghai Jiao Tong University School of Medicine, Shanghai 200030, China.
| | - Danping Hong
- The Affiliated Brain Hospital, Guangzhou Medical University, Guangzhou 510370, China; Key Laboratory of Neurogenetics and Channelopathies of Guangdong Province and the Ministry of Education of China, Guangzhou Medical University, Guangzhou 510370, China; Institute of Psychiatry and Psychology, The Affiliated Brain Hospital, Guangzhou Medical University, Guangzhou 510370, China.
| | - Han Yang
- The Affiliated Brain Hospital, Guangzhou Medical University, Guangzhou 510370, China; Institute of Psychiatry and Psychology, The Affiliated Brain Hospital, Guangzhou Medical University, Guangzhou 510370, China.
| | - Zhihang Zhu
- The Affiliated Brain Hospital, Guangzhou Medical University, Guangzhou 510370, China; Key Laboratory of Neurogenetics and Channelopathies of Guangdong Province and the Ministry of Education of China, Guangzhou Medical University, Guangzhou 510370, China; Institute of Psychiatry and Psychology, The Affiliated Brain Hospital, Guangzhou Medical University, Guangzhou 510370, China.
| | - Daomeng Cheng
- The Affiliated Brain Hospital, Guangzhou Medical University, Guangzhou 510370, China; Key Laboratory of Neurogenetics and Channelopathies of Guangdong Province and the Ministry of Education of China, Guangzhou Medical University, Guangzhou 510370, China; Institute of Psychiatry and Psychology, The Affiliated Brain Hospital, Guangzhou Medical University, Guangzhou 510370, China.
| | - Caiping Dang
- The Affiliated Brain Hospital, Guangzhou Medical University, Guangzhou 510370, China; School of Health Management, Guangzhou Medical University, Guangzhou 511436, China; Institute of Psychiatry and Psychology, The Affiliated Brain Hospital, Guangzhou Medical University, Guangzhou 510370, China.
| | - Yan Song
- State Key Laboratory of Cognitive Neuroscience and Learning and IDG/McGovern Institute for Brain Research, Beijing Normal University, Beijing 100875, China; Center for Collaboration and Innovation in Brain and Learning Sciences, Beijing Normal University, Beijing 100875, China.
| | - Chanjuan Yang
- The Affiliated Brain Hospital, Guangzhou Medical University, Guangzhou 510370, China; Key Laboratory of Neurogenetics and Channelopathies of Guangdong Province and the Ministry of Education of China, Guangzhou Medical University, Guangzhou 510370, China; Institute of Psychiatry and Psychology, The Affiliated Brain Hospital, Guangzhou Medical University, Guangzhou 510370, China.
| | - Weizhen Yin
- The Affiliated Brain Hospital, Guangzhou Medical University, Guangzhou 510370, China; Key Laboratory of Neurogenetics and Channelopathies of Guangdong Province and the Ministry of Education of China, Guangzhou Medical University, Guangzhou 510370, China; Institute of Psychiatry and Psychology, The Affiliated Brain Hospital, Guangzhou Medical University, Guangzhou 510370, China.
| | - Yanling Zhou
- The Affiliated Brain Hospital, Guangzhou Medical University, Guangzhou 510370, China; Key Laboratory of Neurogenetics and Channelopathies of Guangdong Province and the Ministry of Education of China, Guangzhou Medical University, Guangzhou 510370, China; Institute of Psychiatry and Psychology, The Affiliated Brain Hospital, Guangzhou Medical University, Guangzhou 510370, China.
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12
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Wei M, Luo X, Fu J, Dong YS, Liu J, Li X, Dong GH. Approach bias modification reduces automatic gaming tendencies and enhances brain synchronization in internet gaming disorder. J Psychiatr Res 2025; 186:263-272. [PMID: 40262287 DOI: 10.1016/j.jpsychires.2025.04.012] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Track Full Text] [Journal Information] [Submit a Manuscript] [Subscribe] [Scholar Register] [Received: 11/14/2024] [Revised: 03/05/2025] [Accepted: 04/08/2025] [Indexed: 04/24/2025]
Abstract
BACKGROUND Automatic approaches to gaming-related cues are key factors in internet gaming disorder (IGD). Approach bias modification (ApBM) has been shown to reduce addictive behaviors, but its neurobiological effects remain poorly understood. This study examined changes in brain activities in the 'natural' state in IGD patients after ApBM. METHODS Fifty-five (of 61) IGD patients were randomly assigned to the approach-avoidance task (AAT, n = 30) and sham-AAT (n = 25) groups. Participants completed the pre-test, five real/sham ApBM sessions, and the post-test. In the pre-and post-tests, fMRI data were collected while viewing gaming and neutral videos. Inter-subject correlation (ISC) and functional connectivity (FC) analyses were conducted to explore the ApBM-related changes. RESULTS ANOVA of behavioral data revealed that ApBM significantly decreased the approach bias and addiction scores. The ISC analyses revealed increased synchronization in the paracentral lobule, precuneus, and insula regions in the ATT group after ApBM. Additionally, decreased FC was observed between the insula and superior frontal gyrus, precuneus, and orbitofrontal cortex in the AAT group. CONCLUSIONS Preliminary findings suggest that ApBM may be effective in reducing automatic approach tendencies toward gaming cues, highlighting its potential as an intervention strategy. However, it is important to note that the neurobiological evidence in this study only provides a possible association, and the results should be interpreted with caution. Future research is needed to further examine the clinical efficacy of ApBM in IGD, whether as a stand-alone treatment or as an adjunct to formal therapy.
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Affiliation(s)
- Meiting Wei
- Department of Psychology, Yunnan Normal University, Kunming, Yunnan province, PR China
| | - Xin Luo
- Department of Psychology, Yunnan Normal University, Kunming, Yunnan province, PR China
| | - Jiejie Fu
- Center for Cognition and Brain Disorders, The Affiliated Hospital of Hangzhou Normal University, Hangzhou, Zhejiang Province, PR China
| | - Yi-Sheng Dong
- Department of Psychology and Behavioral Sciences, Zhejiang University, Hangzhou, Zhejiang Province, PR China
| | - Jiang Liu
- Department of Psychology, Yunnan Normal University, Kunming, Yunnan province, PR China
| | - Xuzhou Li
- Department of Psychology, Yunnan Normal University, Kunming, Yunnan province, PR China
| | - Guang-Heng Dong
- Department of Psychology, Yunnan Normal University, Kunming, Yunnan province, PR China.
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13
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Chakravarthula PN, Suffridge JE, Wang S. Gaze dynamics during natural scene memorization and recognition. Cognition 2025; 259:106098. [PMID: 40054396 DOI: 10.1016/j.cognition.2025.106098] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Track Full Text] [Journal Information] [Subscribe] [Scholar Register] [Received: 11/25/2024] [Revised: 02/21/2025] [Accepted: 02/24/2025] [Indexed: 04/09/2025]
Abstract
Humans can rapidly memorize numerous images, which is surprising considering the limited visual sampling of each image. To enhance the probability of recognition, it is crucial to focus on previously sampled locations most likely to support memory. How does the visuomotor system achieve this? To study this, we analyzed the eye movements of a group of neurotypical observers while they performed a natural scene memorization task. Using comprehensive gaze analysis and computational modeling, we show that observers traded off visual exploration for exploiting information at the most memorable scene locations with repeated viewing. Furthermore, both the explore-exploit trade-off and gaze consistency predicted accurate recognition memory. Finally, false alarms were predicted by confusion of the incoming visual information at fixated locations with previously sampled information from other images. Together, our findings shed light on the symbiotic relationship between attention and memory in facilitating accurate natural scene memory.
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Affiliation(s)
| | - Jacob E Suffridge
- Rockefeller Neuroscience Institute, West Virginia University, Morgantown, WV 26506, USA
| | - Shuo Wang
- Department of Radiology, Washington University in St. Louis, St. Louis, MO 63110, USA.
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14
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Lee TW, Tramontano G. Inverse relationship between nodal strength and nodal power: Insights from separate resting fMRI and EEG datasets. J Neurosci Methods 2025; 418:110438. [PMID: 40180158 DOI: 10.1016/j.jneumeth.2025.110438] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Track Full Text] [Journal Information] [Subscribe] [Scholar Register] [Received: 03/25/2024] [Revised: 02/15/2025] [Accepted: 03/27/2025] [Indexed: 04/05/2025]
Abstract
BACKGROUND Regional neural response and network properties have traditionally been studied separately. However, growing evidence suggests a close interplay between regional activity and inter-regional connectivity. This study aimed to examine the relationship between global functional connectivity and regional spontaneous activity, termed the global-to-local relationship. NEW METHOD Resting-state fMRI data were parcellated using MOSI (modular analysis and similarity measurements), enabling multi-resolution functional partitioning. For each parcellated cluster, the mean amplitude of low-frequency fluctuations (node power) and its average functional connectivity with the remaining cortex (node strength) were computed. Correlation analyses assessed their relationship. A supplementary analysis was conducted on EEG data (1-30 Hz). RESULTS A significant negative correlation between node strength and regional power was observed in MRI datasets. One-sample t-tests confirmed robustness across different MOSI resolutions, with individual P values at the level 10-4 to 10-5. The negative relationship was also found in EEG data but was restricted to delta (1-4 Hz) and theta (4-8 Hz) bands. COMPARISON WITH EXISTING METHODS This study introduces two key novel aspects. First, it applies MOSI to the entire cortex, enhancing the comprehensiveness of network analysis. Second, it examines the global influence on regional neural activity, rather than limiting the focus to a specific network. CONCLUSIONS A robust negative relationship between node strength and node power was consistently observed across both MRI and EEG datasets, particularly in lower frequency bands (up to 8 Hz). These findings suggest a framework for investigating how global connectivity shapes regional neural activity, with inhibitory coupling as a potential underlying mechanism.
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Affiliation(s)
- Tien-Wen Lee
- The NeuroCognitive Institute (NCI) Clinical Research Foundation, Mt Arlington, NJ, USA.
| | - Gerald Tramontano
- The NeuroCognitive Institute (NCI) Clinical Research Foundation, Mt Arlington, NJ, USA.
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15
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Liu C, Wang J, Li H, Shangguan Q, Jin W, Zhu W, Wang P, Chen X, Wang Q. Loss aversion and evidence accumulation in short-video addiction: A behavioral and neuroimaging investigation. Neuroimage 2025; 313:121250. [PMID: 40324736 DOI: 10.1016/j.neuroimage.2025.121250] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Track Full Text] [Journal Information] [Subscribe] [Scholar Register] [Received: 12/17/2024] [Revised: 05/02/2025] [Accepted: 05/02/2025] [Indexed: 05/07/2025] Open
Abstract
Excessive use of short-video platforms not only impairs decision-making processes but also predisposes individuals to addictive behaviors. This study investigated the relationship between short-video addiction (SVA) symptoms and loss aversion (LA), delving into the underlying computational and neural mechanisms using the drift diffusion model (DDM) and the inter-subject representational similarity analysis (IS-RSA). Behavioral analyses revealed a significant negative correlation between SVA symptoms and the LA coefficient (lnλ). Additionally, the DDM-based drift rate (v) was found to mediate this relationship. Neuroimaging analyses further indicated that SVA symptoms were negatively associated with gain-related activity in the right precuneus, while positively correlating with loss-related activity in the right cerebellum and left postcentral gyrus. Notably, precuneus activation during gain processing mediated the relationship between SVA symptoms and both lnλ and drift rate. IS-RSA revealed that inter-subject variations in SVA symptoms were significantly associated with distinct activation patterns related to gain processing in the frontoparietal network (e.g., frontal pole, inferior frontal gyrus, and supramarginal gyrus) and motor network (e.g., precentral), as well as loss-related activation patterns in the motor networks (e.g., postcentral and pre-supplementary motor area). Similar patterns emerged when examining simultaneous gain and loss-related activation patterns. Mediation analyses further demonstrated that functional activation patterns in the motor network mediated the relationships between inter-subject variations in SVA symptoms and both loss-aversion and psychological processing patterns (e.g., decision threshold, drift rate, and non-decision time). These findings provide novel insights into the cognitive and neural mechanisms underlying the influence of SVA symptoms on loss aversion, and suggest the critical roles of evidence accumulation speed and specific brain activation patterns-particularly within the cognitive control and motor network-in shaping decision-making biases associated with addiction.
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Affiliation(s)
- Chang Liu
- Faculty of Psychology, Tianjin Normal University, Tianjin 300387, PR China
| | - Jinlian Wang
- Faculty of Psychology, Tianjin Normal University, Tianjin 300387, PR China
| | - Hanbing Li
- Faculty of Psychology, Tianjin Normal University, Tianjin 300387, PR China
| | - Qianyi Shangguan
- Faculty of Psychology, Tianjin Normal University, Tianjin 300387, PR China
| | - Weipeng Jin
- Department of Neurosurgery, Tianjin Huanhu Hospital, Tianjin 300060, PR China
| | - Wenwei Zhu
- School of Psychology, South China Normal University, Guangzhou 510631, PR China
| | - Pinchun Wang
- College of Early Childhood Education, Tianjin Normal University, Tianjin 300387, PR China
| | - Xuyi Chen
- Characteristic Medical Center of People's Armed Police Forces, Tianjin 300162, PR China.
| | - Qiang Wang
- Faculty of Psychology, Tianjin Normal University, Tianjin 300387, PR China; State Key Laboratory of Cognitive Neuroscience and Learning & IDG/McGovern Institute for Brain Research, Beijing Normal University, Beijing 100875, PR China.
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16
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Zhou Y, Thompson B. Attention deficits in Amblyopia: A narrative review. Vision Res 2025; 231:108606. [PMID: 40288046 DOI: 10.1016/j.visres.2025.108606] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Track Full Text] [Journal Information] [Subscribe] [Scholar Register] [Received: 03/01/2025] [Revised: 04/12/2025] [Accepted: 04/15/2025] [Indexed: 04/29/2025]
Abstract
Amblyopia has effects on vision that extend from the processing of low-level visual features to higher level functions such as visual attention. In this narrative review, we focus on the impact of amblyopia on visual attention. A structured literature search revealed 28 articles reporting comparisons between amblyopia and normal vision control groups for a variety of visual attention tasks. Several of these articles also included neuroimaging measures. A review of these articles suggested that amblyopia does not affect behavioral performance of tasks with a low attentional load, such as cuing tasks, but deficits emerge for tasks with high demands on visual attention such as multiple object tracking. Deficits are not limited to the amblyopic eye but are also evident under fellow eye and binocular viewing conditions suggesting that abnormal early binocular visual experience can fundamentally alter the development of visual attention. Overall, the current literature suggests that amblyopia is associated with reduced visual attention resources. We raise the possibility that this attention resource deficit may be partially associated with an attentional demand for suppression of the amblyopic eye.
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Affiliation(s)
- Yuntao Zhou
- Centre for Eye and Vision Research, 17W Science Park, Hong Kong
| | - Benjamin Thompson
- Centre for Eye and Vision Research, 17W Science Park, Hong Kong; School of Optometry and Vision Science, University of Waterloo, Waterloo, Ontario, Canada; Liggins Institute, University of Auckland, Auckland, New Zealand.
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17
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Rettie L, Marsh JE, Liversedge SP, Wang M, Degno F. Auditory distraction during reading: Investigating the effects of background sounds on parafoveal processing. Q J Exp Psychol (Hove) 2025; 78:1017-1040. [PMID: 39085167 PMCID: PMC12095895 DOI: 10.1177/17470218241269327] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Track Full Text] [Download PDF] [Figures] [Journal Information] [Subscribe] [Scholar Register] [Received: 04/16/2021] [Revised: 05/22/2024] [Accepted: 05/22/2024] [Indexed: 08/02/2024]
Abstract
Previous research suggests that unexpected (deviant) sounds negatively affect reading performance by inhibiting saccadic planning, which models of reading agree takes place simultaneous to parafoveal processing. This study examined the effect of deviant sounds on foveal and parafoveal processing. Participants read single sentences in quiet, standard (repeated sounds), or deviant sound conditions (a new sound within a repeated sound sequence). Sounds were presented with a variable delay coincident with the onset of fixations on target words during a period when saccadic programming and parafoveal processing occurred. We used the moving window paradigm to manipulate the amount of information readers could extract from the parafovea (the entire sentence or a 13-character window of text). Global, sentence-level analyses showed typical disruption to reading by the window, and under quiet conditions similar effects were observed at the target and post-target word in the local analyses. Standard and deviant sounds also produced clear distraction effects of differing magnitudes at the target and post-target words, though at both regions, these effects were qualified by interactions. Effects at the target word suggested that with sounds, readers engaged in less effective parafoveal processing than under quiet. Similar patterns of effects due to standard and deviant sounds, each with a different time course, occurred at the post-target word. We conclude that distraction via auditory deviation causes disruption to parafoveal processing during reading, with such effects being modulated by the degree to which a sound's characteristics are more or less unique.
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Affiliation(s)
- Laura Rettie
- School of Psychology and Humanities, University of Central Lancashire, Preston, UK
| | - John E Marsh
- School of Psychology and Humanities, University of Central Lancashire, Preston, UK
- Engineering Psychology, Humans and Technology, Department of Business Administration, Technology and Social Sciences, Luleå University of Technology, Luleå, Sweden
| | - Simon P Liversedge
- School of Psychology and Humanities, University of Central Lancashire, Preston, UK
| | - Mengsi Wang
- Faculty of Psychology, Tianjin Normal University, Tianjin, China
| | - Federica Degno
- Department of Psychology, Bournemouth University, Poole, UK
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18
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Bonfanti D, Bertacco E, Parra LC, Mazzi C, Savazzi S. Electrophysiological hemispheric asymmetries induced by parietal stimulation eliciting visual percepts. Clin Neurophysiol 2025; 174:131-147. [PMID: 40273616 DOI: 10.1016/j.clinph.2025.03.041] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Track Full Text] [Journal Information] [Subscribe] [Scholar Register] [Received: 07/25/2024] [Revised: 02/24/2025] [Accepted: 03/31/2025] [Indexed: 04/26/2025]
Abstract
OBJECTIVE We aimed to establish if the electrophysiological activity resulting from the direct stimulation of the intraparietal sulcus and eliciting visual percepts is hemispheric-specific. METHODS We tested nineteen participants. Each received 360 TMS pulses at phosphene threshold intensity over right and left IPS while recording EEG. After each pulse, participants had to report if they had seen a phosphene. RESULTS Parietal phosphene perception is associated with hemispheric-specific activations: phosphenes elicited by left TMS involve central and frontal electrodes at about 30 ms, and frontal, central and parieto-occipital electrodes from 120 to 250 ms; phosphenes elicited by right parietal TMS involve parietal and centro-parietal electrodes at about 60 ms, and frontal, central and parietal electrodes from 150 to 250 ms. Correlated Component Analysis shows that primary visual areas are not activated when phosphenes are produced by TMS over IPS. CONCLUSIONS Our results show that direct stimulation of IPS gives rise to sustained patterns of activity specific to the stimulated hemisphere. Moreover, elicited parietal phosphenes are associated with evoked activity specific to the stimulated hemisphere and located outside early visual processing areas. SIGNIFICANCE This study highlights hemispheric differences in the electrophysiological dynamics related to parietal phosphenes, and shows that the dorsal pathway can give rise to visual conscious percepts.
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Affiliation(s)
- D Bonfanti
- Perception and Awareness Lab, Department of Neuroscience, Biomedicine and Movement Sciences, University of Verona, Verona, Italy
| | - E Bertacco
- Perception and Awareness Lab, Department of Neuroscience, Biomedicine and Movement Sciences, University of Verona, Verona, Italy
| | - L C Parra
- Department of Biomedical Engineering, City College of New York, New York, USA
| | - C Mazzi
- Perception and Awareness Lab, Department of Neuroscience, Biomedicine and Movement Sciences, University of Verona, Verona, Italy.
| | - S Savazzi
- Perception and Awareness Lab, Department of Neuroscience, Biomedicine and Movement Sciences, University of Verona, Verona, Italy
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19
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Ye L, Ba L, Si H, Yan D. Study on resting-state brain network alterations in flight trainees based on independent component analysis. Neuroscience 2025:S0306-4522(25)00669-4. [PMID: 40449681 DOI: 10.1016/j.neuroscience.2025.05.305] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [Track Full Text] [Journal Information] [Subscribe] [Scholar Register] [Received: 03/15/2025] [Revised: 05/26/2025] [Accepted: 05/28/2025] [Indexed: 06/03/2025]
Abstract
This study aimed to investigate the functional alterations in the resting-state brain networks of flight trainees using the independent component analysis (ICA) method. A total of 33 flight trainees and 33 general college students were recruited. Resting-state fMRI data were collected using a 3.0 T MRI scanner. ICA was employed to extract resting-state brain network components, followed by statistical analyses. Fourteen physiologically independent components were identified during the ICA process and classified into nine networks. The flight trainees exhibited significantly increased activation in the right calcarine fissure within the ventral attention network (FWE corrected, P < 0.05). Moreover, the region of interest values of the differential brain region in flight trainees showed a significant positive correlation with the correct rate of the Berg Card Sorting Test (BCST) and a significant negative correlation with the BCST perseverative error (P < 0.05 for both). The significant activation of the right calcarine fissure of flight trainees may be associated with the high attentional demands of flight tasks. Flight trainees demonstrated superior executive function and attention allocation abilities, providing evidence of adaptive functional adjustments in the brain caused by professional activities.
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Affiliation(s)
- Lu Ye
- College of Geheral Aviation and Flight, Nanjing University of Aeronautics and Astronautics, Nanjing 211106, China; Institute of Flight Technology, Civil Aviation Flight University of China, Guanghan 618307, China
| | - Liya Ba
- Institute of Flight Technology, Civil Aviation Flight University of China, Guanghan 618307, China
| | - Haiqing Si
- College of Geheral Aviation and Flight, Nanjing University of Aeronautics and Astronautics, Nanjing 211106, China.
| | - Dongfeng Yan
- Institute of Flight Technology, Civil Aviation Flight University of China, Guanghan 618307, China
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20
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Hernández D, Puupponen A, Keränen J, Vandenitte S, Anible B, Ortega G, Jantunen T. Neuroelectrical and behavioral correlates of constructed action recognition in Finnish Sign language. Neuroscience 2025; 575:140-149. [PMID: 40132792 DOI: 10.1016/j.neuroscience.2025.03.046] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Track Full Text] [Journal Information] [Subscribe] [Scholar Register] [Received: 11/07/2024] [Revised: 01/30/2025] [Accepted: 03/19/2025] [Indexed: 03/27/2025]
Abstract
Language can be processed with varying levels of attentional involvement; consequently, the interplay between the language and attentional systems in the brain has been extensively studied in spoken languages. However, in signed languages (SLs), this interplay is less well understood. Here, we use Constructed Action (CA) - a meaning-making strategy based on enactment - as a window into the attentional mechanisms recruited in signed language comprehension. We explored the attentional processing of CA by identifying the sequence of processes involved and in which stage CA and its types might be processed differently. Finally, we investigated the associations between the brain mechanisms of CA detection and their behavioral manifestations, as well as with components of attention of the Attention Network Test (ANT). We also measured the electrophysiological correlates of performance on an oddball CA detection task in deaf and hearing L1 signers. We found that processes involved in all signers' active detection of CA involved automatic (indexed by N1 and P2) and attention-based processes (indexed by N2s and P3s). N2 posterior bilateral were also more negative for tokens of overt CA than for PT-only signs, while P3a was more positive for all types of CA than for PT. No significant results were found regarding the ANT. We conclude that specific attentional involvement in CA detection is triggered by the increasing enacting elements and saliency involved in CA. This study yielded new insights into the functional interaction between the neural mechanisms underlying attentional control and those mediating CA processing in SL.
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Affiliation(s)
- Doris Hernández
- Sign Language Centre, Department of Language and Communication, University of Jyväskylä, Jyväskylä, Finland; Center for Interdisciplinary Brain Research (CIBR), Department of Psychology, University of Jyväskylä, Jyväskylä, Finland.
| | - Anna Puupponen
- Sign Language Centre, Department of Language and Communication, University of Jyväskylä, Jyväskylä, Finland
| | - Jarkko Keränen
- Sign Language Centre, Department of Language and Communication, University of Jyväskylä, Jyväskylä, Finland
| | - Sébastien Vandenitte
- Sign Language Centre, Department of Language and Communication, University of Jyväskylä, Jyväskylä, Finland
| | - Benjamin Anible
- Department of Language and Literature, NTNU, Trondheim, Norway
| | - Gerardo Ortega
- Department of English Language and Applied Linguistics, University of Birmingham, Birmingham, UK
| | - Tommi Jantunen
- Sign Language Centre, Department of Language and Communication, University of Jyväskylä, Jyväskylä, Finland
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21
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Liu Q, Lin Y, Zhang W. Intersubject correlation as a predictor of attention: a systematic review. BMC Psychol 2025; 13:546. [PMID: 40405228 PMCID: PMC12100797 DOI: 10.1186/s40359-025-02879-7] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Track Full Text] [Download PDF] [Figures] [Journal Information] [Subscribe] [Scholar Register] [Received: 12/18/2024] [Accepted: 05/14/2025] [Indexed: 05/24/2025] Open
Abstract
This meta-analysis examines the challenge of capturing brain activity in real-world and laboratory settings by integrating naturalistic neuroimaging and experimental data with behavioral measures to explore the predictive role of intersubject correlation (ISC) in attention. Using databases such as Web of Science and PubMed, we conducted a comprehensive search from January 2000 to July 2024. Our meta-analysis of 14 studies and 27 effect sizes reveals a significant positive correlation between ISC and attention (r = 0.65, p < 0.001), demonstrating that ISC serves as a reliable neural marker for attentional engagement under various experimental conditions. By incorporating naturalistic stimuli such as video clips and controlled laboratory tasks, we provide insights into the application of ISC to predict attention in ecologically-valid contexts. Moreover, our addition of behavioral data further enhances the understanding of how neural synchronization reflects attentional states. Our results underscore the potential of utilizing ISC to develop personalized assessments and interventions in educational and cognitive settings.
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Affiliation(s)
- Qing Liu
- Zhejiang University of Technology, Hangzhou, China.
| | - Yuhang Lin
- Zhejiang University of Technology, Hangzhou, China
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22
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Kang JU, Mattar L, Vergara J, Gobo VE, Rey HG, Heilbronner SR, Watrous AJ, Hayden BY, Sheth SA, Bartoli E. Parietal cortex is recruited by frontal and cingulate areas to support action monitoring and updating during stopping. Neuroimage 2025; 315:121288. [PMID: 40409386 DOI: 10.1016/j.neuroimage.2025.121288] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [Track Full Text] [Journal Information] [Subscribe] [Scholar Register] [Received: 03/04/2025] [Revised: 05/08/2025] [Accepted: 05/20/2025] [Indexed: 05/25/2025] Open
Abstract
Recent evidence indicates that the intraparietal sulcus (IPS) may play a causal role in action stopping, potentially representing a novel neuromodulation target for inhibitory control dysfunctions. Here, we leverage intracranial recordings in human subjects to establish the timing and directionality of information flow between IPS and prefrontal and cingulate regions during action stopping. Prior to successful inhibition, information flows primarily from the inferior frontal gyrus (IFG), a critical inhibitory control node, to IPS. In contrast, during stopping errors the communication between IPS and IFG is lacking, and IPS is engaged by posterior cingulate cortex, an area outside of the classical inhibition network and typically associated with default mode. Anterior cingulate and orbitofrontal cortex also display performance-dependent connectivity with IPS. Our functional connectivity results provide direct electrophysiological evidence that IPS is recruited by frontal and anterior cingulate areas to support action plan monitoring and updating, and by posterior cingulate during control failures.
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Affiliation(s)
- Jung Uk Kang
- Department of Neurosurgery, Baylor College of Medicine, Houston, TX, USA; Present address: Department of Behavioral Science, The University of Texas MD Anderson Cancer Center, Houston, TX, USA
| | - Layth Mattar
- Department of Neurosurgery, Baylor College of Medicine, Houston, TX, USA
| | - José Vergara
- Department of Neuroscience, Baylor College of Medicine, Houston, TX, USA
| | - Victoria E Gobo
- Department of Neuroscience, Baylor College of Medicine, Houston, TX, USA
| | - Hernan G Rey
- Department of Neurosurgery, Medical College of Wisconsin, Milwaukee, WI, USA
| | - Sarah R Heilbronner
- Department of Neurosurgery, Baylor College of Medicine, Houston, TX, USA; Department of Electrical & Computer Engineering, Rice University, Houston, TX, USA
| | - Andrew J Watrous
- Department of Neurosurgery, Baylor College of Medicine, Houston, TX, USA
| | - Benjamin Y Hayden
- Department of Neurosurgery, Baylor College of Medicine, Houston, TX, USA; Department of Neuroscience, Baylor College of Medicine, Houston, TX, USA; Department of Electrical & Computer Engineering, Rice University, Houston, TX, USA
| | - Sameer A Sheth
- Department of Neurosurgery, Baylor College of Medicine, Houston, TX, USA; Department of Neuroscience, Baylor College of Medicine, Houston, TX, USA; Department of Electrical & Computer Engineering, Rice University, Houston, TX, USA; Menninger Department of Psychiatry and Behavioral Sciences, Baylor College of Medicine, Houston, TX, USA
| | - Eleonora Bartoli
- Department of Neurosurgery, Baylor College of Medicine, Houston, TX, USA; Department of Electrical & Computer Engineering, Rice University, Houston, TX, USA.
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23
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Cheng YP, Nordin AD. Effects of Matched and Mismatched Visual Flow and Gait Speeds on Human Electrocortical Spectral Power. Brain Sci 2025; 15:531. [PMID: 40426701 PMCID: PMC12109666 DOI: 10.3390/brainsci15050531] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [Grants] [Track Full Text] [Download PDF] [Figures] [Journal Information] [Subscribe] [Scholar Register] [Received: 05/04/2025] [Revised: 05/13/2025] [Accepted: 05/20/2025] [Indexed: 05/29/2025] Open
Abstract
Background/Objectives: Visuomotor integration relies on synchronized proprioceptive and visual feedback during visually guided locomotion. How the human brain processes unimodal or asynchronous multimodal inputs during locomotion is unclear. Methods: Using high-density mobile electroencephalography (EEG) and motion capture in a virtual reality environment, we investigated electrocortical responses during altered treadmill gait speeds (0.5 and 1.5 m/s) and visual flow speeds (0.5×, 1×, and 1.5× gait speed) among 13 healthy human subjects. Experimental conditions included passive viewing of a moving virtual environment, walking in a stationary virtual environment, and walking in a moving environment with synchronous and asynchronous visual flow. Results: At faster gait speed, we identified reduced premotor, sensorimotor, and visual electrocortical beta-band spectral power (13-30 Hz) and greater premotor cortex theta power (4-8 Hz). At faster visual flow speeds, we identified reduced sensorimotor electrocortical beta-band spectral power, reduced alpha (8-13 Hz) and beta power, and greater gamma-band power (30-50 Hz) from the visual cortex. During visual flow and gait speed mismatches, sensorimotor and parietal alpha- and beta-band electrocortical spectral power decreased at faster gait speed. During treadmill walking at 1.5 m/s, parietal electrocortical spectral power increased when visual flow exceeded gait speed. Conclusions: Electrical brain dynamics during human gait identified distinct neural circuits for integrating kinesthetic and visual information during visuomotor conflicts, gated by the parietal cortex.
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Affiliation(s)
- Yu-Po Cheng
- Texas A&M Institute for Neuroscience, Texas A&M University, College Station, TX 77840, USA
- Department of Biomedical Engineering, University of Houston, Houston, TX 77204, USA;
| | - Andrew D. Nordin
- Department of Biomedical Engineering, University of Houston, Houston, TX 77204, USA;
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24
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Rosenblum U, Cocks AJ, Norris M, Kal E, Young WR. Anxiety-related attentional characteristics and their relation to freezing of gait in people with Parkinson's: Cross-validation of the Adapted Gait Specific Attentional Profile (G-SAP). JOURNAL OF PARKINSON'S DISEASE 2025:1877718X251326266. [PMID: 40390627 DOI: 10.1177/1877718x251326266] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [Track Full Text] [Subscribe] [Scholar Register] [Indexed: 05/21/2025]
Abstract
BackgroundAnxiety often exacerbates freezing of gait (FOG) in people with Parkinson's (PwP). Anxiety-related attentional processes and associated processing inefficiencies, like conscious movement processing (CMP) and ruminations, can substantially impact movement control. However, their impact on FOG remains largely unexplored.ObjectiveTo validate an adapted 10-item (1-5 Likert scale) Gait-Specific Attentional Profile (G-SAP) in PwP and assess if adapted G-SAP-subscales (Physiological Arousal, CMP, Rumination, and Processing Inefficiencies) are associated with self-reported FOG frequency.MethodsWe recruited 440 PwP (Mage = 65.5 ± 8.7; 5.8 ± 5.0 years since diagnosis) across the UK. Participants completed the adapted G-SAP and questionnaires on demographics, medical background, and FOG frequency. We assessed adapted G-SAP's internal consistency, structural validity, and subscale scores associations with FOG frequency.ResultsThe adapted G-SAP showed acceptable internal consistency (α≥0.66) and acceptable/good model fit (comparative fit index = 0.976). Physiological Arousal and CMP subscale scores presented weaker correlations for PwP with FOG (PwP + FOG, r = 0.52) compared to PwP without FOG (PwP-FOG, r = 0.77; p = 0.006). Higher Rumination (OR: 1.323, 95%CI: [1.214-1.440]) and Physiological Arousal (OR: 1.195, 95%CI:[1.037-1.377]) were significantly associated with higher FOG frequency, controlling for age, time since diagnosis and balance/gait problems.ConclusionsThe adapted G-SAP is reliable and convenient to measure and identify potentially maladaptive anxiety-related attentional processes that may impact FOG. Results suggest that PwP who experience more worrisome thoughts and greater physiological arousal in daily life are likelier to freeze. Compared to PwP-FOG, for PwP + FOG high physiological arousal was associated with reduced goal-directed focus of attention. Future research will determine if this is a causal risk factor.
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Affiliation(s)
- Uri Rosenblum
- Department of Health Sciences, College of Health, Medicine and Life Sciences, Brunel University London, UK
- Faculty of Health and Life Sciences, University of Exeter, Exeter, UK
- Centre for Clinical and Cognitive Neuroscience, Brunel University London, UK
| | - Adam J Cocks
- Centre for Clinical and Cognitive Neuroscience, Brunel University London, UK
- Division of Sport, Health and Exercise Sciences, College of Health, Medicine and Life Sciences, Brunel University London, UK
| | - Meriel Norris
- Department of Health Sciences, College of Health, Medicine and Life Sciences, Brunel University London, UK
| | - Elmar Kal
- Department of Health Sciences, College of Health, Medicine and Life Sciences, Brunel University London, UK
- Centre for Clinical and Cognitive Neuroscience, Brunel University London, UK
| | - William R Young
- Faculty of Health and Life Sciences, University of Exeter, Exeter, UK
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25
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Cha J, Kennedy KER, Negelspach D, Huskey A, Killgore WDS. Ventral tegmental area functional connectivity as a marker of resilience to sleep deprivation. Neurosci Lett 2025; 859-861:138271. [PMID: 40403830 DOI: 10.1016/j.neulet.2025.138271] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [Track Full Text] [Journal Information] [Subscribe] [Scholar Register] [Received: 03/19/2025] [Revised: 05/13/2025] [Accepted: 05/19/2025] [Indexed: 05/24/2025]
Abstract
OBJECTIVE Sleep deprivation (SD) impairs cognitive functions like attention and reaction speed, though some individuals exhibit a trait-like resilience to these effects. To explore the neurobiological basis of this resilience, we quantified cognitive performance using the Percentage Reaction Speed Change (PRSC) from the psychomotor vigilance test (PVT). We then examined the relationship between PRSC and ventral tegmental area (VTA) functional connectivity during 28 h of SD. METHODS Forty-four healthy adults (21 females; age = 25.4 ± 5.6 years) underwent a resting-state functional MRI (rs-fMRI) to examine whole-brain VTA connectivity. Within the same week, participants completed a 28-hour SD protocol, during which PVT performance was measured. We examined the association between VTA connectivity and PRSC, with a focus on connections to the Primary Visual Cortex (V1) and Supplementary and Cingulate Eye Field (SCEF). RESULTS Greater VTA connectivity with the V1 and SCEF was associated with higher PRSC, suggesting that stronger VTA connectivity to these visual processing and cognitive control regions supports cognitive resilience to SD. CONCLUSION The VTA contributes to cognitive resilience during sleep deprivation through its connectivity with visual and cognitive control regions. These findings provide insight into neural mechanisms that help preserve cognitive performance under SD.
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Affiliation(s)
- Jungwon Cha
- Social, Cognitive, & Affective Neuroscience Laboratory, Department of Psychiatry, University of Arizona, 1501 N. Campbell Avenue, Tucson, AZ 85724, USA.
| | - Kathryn E R Kennedy
- Social, Cognitive, & Affective Neuroscience Laboratory, Department of Psychiatry, University of Arizona, 1501 N. Campbell Avenue, Tucson, AZ 85724, USA.
| | - David Negelspach
- Social, Cognitive, & Affective Neuroscience Laboratory, Department of Psychiatry, University of Arizona, 1501 N. Campbell Avenue, Tucson, AZ 85724, USA.
| | - Alisa Huskey
- Social, Cognitive, & Affective Neuroscience Laboratory, Department of Psychiatry, University of Arizona, 1501 N. Campbell Avenue, Tucson, AZ 85724, USA.
| | - William D S Killgore
- Social, Cognitive, & Affective Neuroscience Laboratory, Department of Psychiatry, University of Arizona, 1501 N. Campbell Avenue, Tucson, AZ 85724, USA.
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26
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Liang X, Luo J, Bi Q, Jiang Y, Yang L, Vatansever D, Jefferies E, Gong G. Functional divergence between the two cerebral hemispheres contributes to human fluid intelligence. Commun Biol 2025; 8:764. [PMID: 40382492 PMCID: PMC12085609 DOI: 10.1038/s42003-025-08151-3] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Grants] [Track Full Text] [Download PDF] [Figures] [Journal Information] [Subscribe] [Scholar Register] [Received: 08/23/2024] [Accepted: 04/30/2025] [Indexed: 05/20/2025] Open
Abstract
Hemispheric lateralization is linked to potential cognitive advantages. It is considered a driving force behind the generation of human intelligence. However, establishing quantitative links between the degree of lateralization and intelligence in humans remains elusive. In this study, we propose a framework that utilizes the functional aligned multidimensional representation space derived from hemispheric functional gradients to compute between-hemisphere distances within this space. Applying this framework to a large cohort (N = 777), we identified high functional divergence across the two hemispheres within the frontoparietal network. We found that both global divergence between the cerebral hemispheres and regional divergence within the multiple demand network were positively associated with fluid composite score and partially mediated the relationship between brain size and individual differences in fluid intelligence. Together, these findings deepen our understanding of hemispheric lateralization as a fundamental organizational principle of the human brain, providing empirical evidence for its role in supporting fluid intelligence.
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Affiliation(s)
- Xinyu Liang
- State Key Laboratory of Cognitive Neuroscience and Learning & IDG/McGovern Institute for Brain Research, Beijing Normal University, Beijing, China.
- The Institute of Science and Technology for Brain-inspired Intelligence (ISTBI), Fudan University, Shanghai, China.
| | - Junhao Luo
- State Key Laboratory of Cognitive Neuroscience and Learning & IDG/McGovern Institute for Brain Research, Beijing Normal University, Beijing, China
- Shenzhen CyberAray Network Technology Co. Ltd, Shenzhen, China
- Harbin Institute of Technology, Shenzhen, Shenzhen, China
| | - Qiuhui Bi
- School of Artificial Intelligence, Beijing Normal University, Beijing, China
| | - Yaya Jiang
- State Key Laboratory of Cognitive Neuroscience and Learning & IDG/McGovern Institute for Brain Research, Beijing Normal University, Beijing, China
- Artificial Intelligence and Language Cognition Laboratory, Beijing International Studies University, Beijing, China
| | - Liyuan Yang
- State Key Laboratory of Cognitive Neuroscience and Learning & IDG/McGovern Institute for Brain Research, Beijing Normal University, Beijing, China
| | - Deniz Vatansever
- The Institute of Science and Technology for Brain-inspired Intelligence (ISTBI), Fudan University, Shanghai, China
| | | | - Gaolang Gong
- State Key Laboratory of Cognitive Neuroscience and Learning & IDG/McGovern Institute for Brain Research, Beijing Normal University, Beijing, China.
- Beijing Key Laboratory of Brain Imaging and Connectomics, Beijing Normal University, Beijing, China.
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27
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Anderson MC, Crespo-Garcia M, Subbulakshmi S. Brain mechanisms underlying the inhibitory control of thought. Nat Rev Neurosci 2025:10.1038/s41583-025-00929-y. [PMID: 40379896 DOI: 10.1038/s41583-025-00929-y] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Track Full Text] [Journal Information] [Subscribe] [Scholar Register] [Accepted: 04/25/2025] [Indexed: 05/19/2025]
Abstract
Controlling action and thought requires the capacity to stop mental processes. Over the past two decades, evidence has grown that a domain-general inhibitory control mechanism supported by the right lateral prefrontal cortex achieves these functions. However, current views of the neural mechanisms of inhibitory control derive largely from research into the stopping of action. Whereas action stopping is a convenient empirical model, it does not invoke thought inhibition and cannot be used to identify the unique features of this process. Here, we review research that addresses how organisms stop a key process that drives thoughts: memory retrieval. This work has shown that retrieval stopping shares right dorsolateral and ventrolateral prefrontal mechanisms with action stopping, consistent with a domain-general inhibitory control mechanism, but also recruits a distinct fronto-temporal pathway that determines the success of mental control. As part of this pathway, GABAergic inhibition within the hippocampus influences the efficacy of prefrontal control over thought. These unique elements of mental control suggest that hippocampal disinhibition is a transdiagnostic factor underlying intrusive thinking, linking the fronto-temporal control pathway to preclinical models of psychiatric disorders and fear extinction. We suggest that retrieval-stopping deficits may underlie the intrusive thinking that is common across many psychiatric disorders.
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Affiliation(s)
- Michael C Anderson
- MRC Cognition and Brain Sciences Unit, University of Cambridge, Cambridge, UK.
- Behavioural and Clinical Neurosciences Unit, University of Cambridge, Cambridge, UK.
| | - Maite Crespo-Garcia
- MRC Cognition and Brain Sciences Unit, University of Cambridge, Cambridge, UK
| | - S Subbulakshmi
- Department of Psychology, Stanford University, Stanford, CA, USA
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28
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Khalaf A, Lopez E, Li J, Horn A, Edlow BL, Blumenfeld H. Shared subcortical arousal systems across sensory modalities during transient modulation of attention. Neuroimage 2025; 312:121224. [PMID: 40250641 DOI: 10.1016/j.neuroimage.2025.121224] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Track Full Text] [Journal Information] [Subscribe] [Scholar Register] [Received: 02/03/2025] [Revised: 04/15/2025] [Accepted: 04/15/2025] [Indexed: 04/20/2025] Open
Abstract
Subcortical arousal systems are known to play a key role in controlling sustained changes in attention and conscious awareness. Recent studies indicate that these systems have a major influence on short-term dynamic modulation of visual attention, but their role across sensory modalities is not fully understood. In this study, we investigated shared subcortical arousal systems across sensory modalities during transient changes in attention using block and event-related fMRI paradigms. We analyzed massive publicly available fMRI datasets collected while 1561 participants performed visual, auditory, tactile, and taste perception tasks. Our analyses revealed a shared circuit of subcortical arousal systems exhibiting early transient increases in activity in midbrain reticular formation and central thalamus across perceptual modalities, as well as less consistent increases in pons, hypothalamus, basal forebrain, and basal ganglia. Identifying these networks is critical for understanding mechanisms of normal attention and consciousness and may help facilitate subcortical targeting for therapeutic neuromodulation.
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Affiliation(s)
- Aya Khalaf
- Department of Neurology, Yale University School of Medicine, New Haven, CT, USA
| | - Erick Lopez
- Department of Neurology, Yale University School of Medicine, New Haven, CT, USA
| | - Jian Li
- Department of Neurology, Center for Neurotechnology and Neurorecovery, Massachusetts General Hospital and Harvard Medical School, Boston, MA, USA; Athinoula A. Martinos Center for Biomedical Imaging, Massachusetts General Hospital and Harvard Medical School, Charlestown, MA, USA
| | - Andreas Horn
- Department of Neurology, Center for Neurotechnology and Neurorecovery, Massachusetts General Hospital and Harvard Medical School, Boston, MA, USA; Department of Neurology, Center for Brain Circuit Therapeutics, Brigham & Women's Hospital and Harvard Medical School, Boston, MA, USA; Department of Neurosurgery, Massachusetts General Hospital and Harvard Medical School, Boston, MA, USA; Movement Disorders & Neuromodulation Section, Department of Neurology, Charité - Universitätsmedizin, Berlin, Germany
| | - Brian L Edlow
- Department of Neurology, Center for Neurotechnology and Neurorecovery, Massachusetts General Hospital and Harvard Medical School, Boston, MA, USA; Athinoula A. Martinos Center for Biomedical Imaging, Massachusetts General Hospital and Harvard Medical School, Charlestown, MA, USA
| | - Hal Blumenfeld
- Department of Neurology, Yale University School of Medicine, New Haven, CT, USA; Department of Neuroscience, Yale University School of Medicine, New Haven, CT, USA; Department of Neurosurgery, Yale University School of Medicine, New Haven, CT, USA.
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29
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Gammeri R, Lucisano S, Zavattaro C, Serra H, Cirillo E, Schintu S, Berti A, Boldreghini M, Albera A, Albera R, Ricci R. Altered orienting of visuospatial attention in patients with vestibular disorders. Cortex 2025; 188:69-80. [PMID: 40409181 DOI: 10.1016/j.cortex.2025.04.016] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [Track Full Text] [Journal Information] [Subscribe] [Scholar Register] [Received: 12/17/2024] [Revised: 04/16/2025] [Accepted: 04/16/2025] [Indexed: 05/25/2025]
Abstract
The vestibular system, one of the earliest sensory systems in vertebrates, is crucial for encoding head and trunk movements. Research in stroke patients with spatial attention deficits and studies manipulating vestibular signals in healthy individuals suggest that the vestibular system is also involved in orienting visuospatial attention. However, the specific interactions between vestibular and attentional systems and the consequences of vestibular pathologies on attentional functions are still poorly understood. In this study, we investigated the impact of vestibular disorders on the orienting of automatic (exogenous) and voluntary (endogenous) attention in patients (N = 16) with acute (AVS), episodic (EVS) or chronic (CVS) vestibular syndromes, who were compared to a control group (N = 16) of age-matched healthy participants. The two groups were assessed using endogenous and exogenous versions of the Posner cueing task. Cognitive functioning and anxiety were evaluated with the Montreal Cognitive Assessment (MoCA) and the Beck Anxiety Inventory (BAI), respectively. Vestibular patients exhibited selective impairments in maintaining voluntary attention in the endogenous task, particularly those with EVS and CVS, compared to the controls. In addition, vestibular alterations influenced the automatic right-lateralized attention system, as evidenced by a reduced rightward attentional bias in the exogenous task in vestibular patients. Anxiety, aging, or the overall cognitive function did not influence the observed attention deficits. The evidence that vestibular disorders differentially affect voluntary and automatic orienting of visuospatial attention has relevant implications for the assessment and treatment of patients with vestibular disorders, the rehabilitation of stroke patients with spatial attention deficits, and space research.
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Affiliation(s)
- Roberto Gammeri
- SAN (Space, Attention and actioN) Lab, Department of Psychology, University of Turin, Turin, Italy.
| | - Sergio Lucisano
- Department of Surgical Sciences, University of Turin, Turin, Italy
| | - Claudio Zavattaro
- SAN (Space, Attention and actioN) Lab, Department of Psychology, University of Turin, Turin, Italy
| | - Hilary Serra
- SAN (Space, Attention and actioN) Lab, Department of Psychology, University of Turin, Turin, Italy
| | - Emanuele Cirillo
- SAN (Space, Attention and actioN) Lab, Department of Psychology, University of Turin, Turin, Italy
| | - Selene Schintu
- Center for Mind/Brain Sciences-CIMeC, University of Trento, Rovereto, Italy; Department of Psychological and Brain Sciences, The George Washington University, Washington DC, United States
| | - Anna Berti
- SAN (Space, Attention and actioN) Lab, Department of Psychology, University of Turin, Turin, Italy
| | | | - Andrea Albera
- Department of Surgical Sciences, University of Turin, Turin, Italy
| | - Roberto Albera
- Department of Surgical Sciences, University of Turin, Turin, Italy
| | - Raffaella Ricci
- SAN (Space, Attention and actioN) Lab, Department of Psychology, University of Turin, Turin, Italy; Department of Psychiatry and Behavioral Sciences, Medical University of South Carolina, Charleston, SC, United States.
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30
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Chak C, Machniak E, Giesbrecht B. Task-irrelevant abrupt onsets differentially impact value-related orienting and maintenance. Atten Percept Psychophys 2025:10.3758/s13414-025-03078-7. [PMID: 40360863 DOI: 10.3758/s13414-025-03078-7] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [Grants] [Track Full Text] [Journal Information] [Subscribe] [Scholar Register] [Accepted: 04/11/2025] [Indexed: 05/15/2025]
Abstract
Physically salient stimuli are potent influences on behavior, but their negative impacts can be reduced in the presence of explicit goal-related cues. Here, we investigated whether goal-related cues associated with value are capable of insulating information from task-irrelevant abrupt onsets during two stages of information processing. Abrupt onsets were shown either after attention-directing cues and before a target (Experiment 1) or after a target that is to be remembered for later report (Experiment 2). The cues indicated the value associated with upcoming target locations, and they were either different in value, indicating that one was more valuable than the other, or equal in value. In both experiments, subjects were instructed to report the target that would earn them the most points (Experiment 1) or money (Experiment 2). In Experiment 1, performance suffered with equal cues, suggesting that orienting to multiple locations increases susceptibility to distraction from physically salient stimuli. In Experiment 2, the same pattern did not appear for abrupt onsets during the retention period; instead, the impact of the physically salient stimulus was dependent upon working memory capacity. The differential impact of abrupt onsets prior to (Experiment 1) and after (Experiment 2) encoding of value-related target locations suggest that physically salient task-irrelevant stimuli influence value-related information processing differently during orienting and maintenance.
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Affiliation(s)
- Carly Chak
- Department of Psychological and Brain Sciences, Institute for Collaborative Biotechnologies, University of California, Santa Barbara, CA, 93106-9660, USA.
| | - Emily Machniak
- Department of Psychological and Brain Sciences, Institute for Collaborative Biotechnologies, University of California, Santa Barbara, CA, 93106-9660, USA
| | - Barry Giesbrecht
- Department of Psychological and Brain Sciences, Institute for Collaborative Biotechnologies, University of California, Santa Barbara, CA, 93106-9660, USA
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Zhang J, Zhu X, Zhou H, Wang S. A large neuronal dataset for natural category-based free-gaze visual search in macaques. Sci Data 2025; 12:779. [PMID: 40355416 PMCID: PMC12069534 DOI: 10.1038/s41597-025-05130-5] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Grants] [Track Full Text] [Download PDF] [Figures] [Journal Information] [Subscribe] [Scholar Register] [Received: 01/23/2025] [Accepted: 05/01/2025] [Indexed: 05/14/2025] Open
Abstract
Goal-directed visual attention is a fundamental cognitive process that demonstrates the brain's remarkable ability to prioritize visual information relevant to specific tasks or objectives. Despite its importance, there is a lack of comprehensive datasets to investigate the underlying neural mechanisms. Here, we present a large naturalistic visual search dataset in which rhesus macaques searched for targets among natural stimuli based on object categories using voluntary eye movements. The stimulus set included 40 images per category across four categories: faces, houses, flowers, and hands. We recorded activity from 6871 units in area V4, 8641 units in the inferior temporal cortex (IT), 5622 units in the orbital frontal cortex (OFC), and 9916 units in the lateral prefrontal cortex (LPFC). These units exhibited diverse receptive fields and selectivity for visual categories. Together, our extensive dataset provides a rich neuronal population across multiple brain areas, enabling a comprehensive analysis of the neural processes underlying goal-directed visual attention.
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Affiliation(s)
- Jie Zhang
- Department of Radiology, Washington University in St. Louis, St. Louis, MO, 63110, USA.
- Peng Cheng Laboratory, Shenzhen, 518000, China.
- Shenzhen Institute of Advanced Technology, Chinese Academy of Sciences, Shenzhen, 518055, China.
| | - Xiaocang Zhu
- Shenzhen Institute of Advanced Technology, Chinese Academy of Sciences, Shenzhen, 518055, China
| | - Huihui Zhou
- Peng Cheng Laboratory, Shenzhen, 518000, China.
- Shenzhen Institute of Advanced Technology, Chinese Academy of Sciences, Shenzhen, 518055, China.
| | - Shuo Wang
- Department of Radiology, Washington University in St. Louis, St. Louis, MO, 63110, USA.
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Dewis H, Metcalf CD, Warner MB, Polfreman R, Godwin HJ. Easy does it: Selection during interactive search tasks is biased towards objects that can be examined easily. Atten Percept Psychophys 2025:10.3758/s13414-025-03083-w. [PMID: 40355682 DOI: 10.3758/s13414-025-03083-w] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [Track Full Text] [Journal Information] [Subscribe] [Scholar Register] [Accepted: 04/16/2025] [Indexed: 05/14/2025]
Abstract
It is well understood that attentional selection is required to deploy visual attention to relevant objects within displays during visual search tasks. Interactive search, an extension of visual search, refers to tasks wherein an individual must manipulate items within their environment to uncover obscured information whilst searching for a target object. Here, we conducted two independent interactive search experiments where participants were asked to interact with virtual cubes to locate a target T shape embedded onto the side of one of the cubes. Our goal here was to investigate the drivers of attentional selection within interactive searches. To do so, we manipulated the effort required to rotate cubes (Experiment 1) and the quantity of shapes attached to the cubes (Experiment 2). Our findings suggest that the perceived effort required to interact with an object is an extremely strong driver of attentional selection within interactive search behaviors. Here, targets may be slower to be detected when that target is obscured within or by an object that conveys, in some shape or form, greater difficulty to examine compared with other objects. These findings provide an exciting first step towards understanding the factors that influence selection during interactive searches. Data and experimental code for all experiments in this study can be accessed online via this web address: https://osf.io/2zyvf/?view_only=ae4f4f2c36ab4e6aae5da3e99fb81988 . Experiments were not preregistered.
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Affiliation(s)
- Haden Dewis
- University of Southampton, Southampton, UK.
- School of Psychology, University of Southampton, Highfield, Southampton, Hampshire, SO17 1BJ, UK.
- Department of Psychology, University of Southampton, Southampton, UK.
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Sharpe BT, Sharpe A, Poulus D, Obine EAC, King R, Birch PDJ, Gladwin TE. Enhancing pressurized esports performance: a pilot study on the combined effects of transcranial direct current stimulation and arousal reappraisal. ANXIETY, STRESS, AND COPING 2025:1-17. [PMID: 40340544 DOI: 10.1080/10615806.2025.2502792] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [Track Full Text] [Subscribe] [Scholar Register] [Received: 05/08/2024] [Revised: 04/30/2025] [Accepted: 05/02/2025] [Indexed: 05/10/2025]
Abstract
BACKGROUND AND OBJECTIVES This pilot study explored the combined impact of arousal reappraisal intervention and transcranial direct current stimulation (tDCS) targeting the left dorsolateral prefrontal cortex (PFC) on state anxiety, challenge and threat appraisals, and performance under high pressure in esport contexts. Arousal reappraisal has previously been shown to enable individuals to interpret physiological arousal more constructively, while tDCS has demonstrated potential to increase the efficacy of psychological interventions. DESIGN A fully repeated measures study design was employed where participants experienced four different experimental interventions: tDCS with arousal reappraisal, tDCS with active control, sham stimulation with arousal reappraisal, and sham stimulation with active control. METHODS Seventeen male Counter-Strike competitors participated in the study. Each participant received all four experimental intervention conditions, with measurements taken of state anxiety, challenge and threat appraisals, and esport performance under pressure. RESULTS The findings tentatively suggest that arousal reappraisal effectively reduces cognitive anxiety, promotes favourable challenge appraisals versus threat, and enhances esports performance. This effect appeared more pronounced when arousal reappraisal was combined with anodal tDCS. CONCLUSIONS Combining arousal reappraisal and tDCS may be a promising intervention for esports competitors facing performance pressure. The synergistic effects of these interventions warrant further investigation in larger samples.
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Affiliation(s)
- B T Sharpe
- Institute of Psychology, Business, and Human Sciences, University of Chichester, Chichester, UK
| | - A Sharpe
- Institute of Psychology, Business, and Human Sciences, University of Chichester, Chichester, UK
| | - D Poulus
- Physical Activity, Sport, and Exercise Research Theme, Faculty of Health, Southern Cross University, Lismore, Australia
| | - E A C Obine
- Institute of Psychology, Business, and Human Sciences, University of Chichester, Chichester, UK
| | - R King
- Institute of Psychology, Business, and Human Sciences, University of Chichester, Chichester, UK
| | - P D J Birch
- Institute of Applied Sciences, University of Chichester, Chichester, UK
| | - T E Gladwin
- Institute for Globally Distributed Open Research and Education (IGDORE), London, UK
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Saccani MS, Contemori G, Del Popolo Cristaldi F, Bonato M. Attentional load impacts multisensory integration, without leading to spatial processing asymmetries. Sci Rep 2025; 15:16240. [PMID: 40346130 PMCID: PMC12064717 DOI: 10.1038/s41598-025-95717-0] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Track Full Text] [Download PDF] [Figures] [Journal Information] [Subscribe] [Scholar Register] [Received: 10/17/2024] [Accepted: 03/24/2025] [Indexed: 05/11/2025] Open
Abstract
The present study examined whether spatial processing in the unimpaired cognitive system is influenced by attentional load during multitasking. More specifically, it tested the hypothesis that high attentional load would induce spatial processing asymmetries in the form of a rightward attentional bias. We conducted two separate experiments on healthy adults (n = 101 and n = 98) by using web-based data collections. We capitalized on a condition of perceptual uncertainty to investigate the presence of these spatial asymmetries which cannot be easily detected under regular perceptual conditions. More specifically, we employed a primary audiovisual integration task, which involved presenting stimuli capable of eliciting the sound-induced flash illusion (i.e., task-relevant flashes accompanied by an incongruent number of sounds) on either the left or right side of the screen. This task enabled us to investigate audiovisual integration, but also indirectly provided an opportunity to sensitively explore spatial processing within a highly complex context. In Experiment 1, attentional load was increased by presenting stimuli to be retained before the audiovisual integration task (i.e., "offline" attentional load manipulation). Differently, in Experiment 2, attentional load was increased by having participants to perform visual discrimination during the audiovisual integration task (i.e., "online" attentional load manipulation). Attentional load was increased in a different way within each experiment to test the idea that more demanding tasks, albeit of different nature, would have similarly modulated performance. In both experiments, we replicated the increase of sound-induced flash illusion under high attentional load, which challenges the notion of an early and pre-attentive onset of the illusion. However, this effect was identical for left- and right-sided flashes, which speaks against the existence of load-induced spatial processing asymmetries in the unimpaired cognitive system. Given that both experiments yielded similar results, quantitative aspects of attentional engagement rather than the nature of the attentional resources involved seem to play a critical role.
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Affiliation(s)
- M S Saccani
- Padova Neuroscience Centre, University of Padua, Via Orus 2, 35129, Padua, Italy.
- Department of General Psychology, University of Padua, Via Venezia 8, 35131, Padua, Italy.
| | - G Contemori
- Department of General Psychology, University of Padua, Via Venezia 8, 35131, Padua, Italy
| | - F Del Popolo Cristaldi
- Department of General Psychology, University of Padua, Via Venezia 8, 35131, Padua, Italy
| | - M Bonato
- Padova Neuroscience Centre, University of Padua, Via Orus 2, 35129, Padua, Italy.
- Department of General Psychology, University of Padua, Via Venezia 8, 35131, Padua, Italy.
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Ma M, Shang Y, Lin X, Han W, Peng Y, Wang S, Niu C, Li H, Zhang M. Aberrant interhemispheric resting state functional connectivity and corpus callosum microstructure in acute carbon monoxide poisoning. Brain Res Bull 2025; 227:111376. [PMID: 40347982 DOI: 10.1016/j.brainresbull.2025.111376] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [Track Full Text] [Journal Information] [Subscribe] [Scholar Register] [Received: 01/13/2025] [Revised: 05/05/2025] [Accepted: 05/06/2025] [Indexed: 05/14/2025]
Abstract
Acute carbon monoxide poisoning (ACOP) is a significant contributor to acute poisoning incidents worldwide, with numerous patients suffering from cognitive impairment. Growing evidence indicates that patients with ACOP exhibit both disrupted functional connectivity and corpus callosum (CC) degeneration. Nevertheless, how interhemispheric connectivity is altered in ACOP and how such alterations relate to cognitive deficits remain largely unexplored. In this study, multimodal magnetic resonance imaging was performed on 30 patients with ACOP and 28 healthy controls (HC), and their cognitive functions were evaluated. Group differences in the voxel-mirrored homotopic connectivity (VMHC) index and CC white matter microstructure were analyzed. Furthermore, mediation analysis was conducted to elucidate the interrelationships among CC integrity, interhemispheric connectivity, and cognitive impairment. Compared to HC, patients with ACOP exhibited reduced VMHC values in the middle frontal gyrus, inferior parietal lobule, precentral gyrus, and temporal regions, along with decreased fractional anisotropy values in the subregions of the CC, including the genu, body, and splenium. Partial correlation analyses showed that VMHC in the inferior parietal lobule positively correlated with Glasgow Coma Scale scores. In addition, VMHC in both the inferior parietal lobule and the middle temporal gyrus positively correlated with Montreal Cognitive Assessment-Basic scores. Mediation analysis indicated that changes in interhemispheric connectivity played a crucial role in mediating the effect of CC integrity on cognitive impairment. Together, these findings may offer novel insights into the neurobiological mechanisms underlying ACOP.
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Affiliation(s)
- Mingyue Ma
- Department of Medical Imaging, the First Affiliated Hospital of Xi'an Jiaotong University, Xi'an, Shaanxi, China; Department of Radiology, the Affiliated Xi'an Central Hospital of Xi'an Jiaotong University, Xi'an, Shaanxi, China
| | - Yu Shang
- School of Future Technology, Xi'an Jiaotong University, Xi'an, Shaanxi, China
| | - Xiaoying Lin
- Department of Medical Imaging, the First Affiliated Hospital of Xi'an Jiaotong University, Xi'an, Shaanxi, China
| | - Wenxuan Han
- Department of Medical Imaging, the First Affiliated Hospital of Xi'an Jiaotong University, Xi'an, Shaanxi, China
| | - Yihao Peng
- Department of Medicine, Xi'an Jiaotong University, Xi'an, Shaanxi, China
| | - Shenghai Wang
- Department of Medical Imaging, the First Affiliated Hospital of Xi'an Jiaotong University, Xi'an, Shaanxi, China; Department of Medical Imaging, Yan'an People's Hospital of Shaanxi Province, Yan'an, Shaanxi, China
| | - Chen Niu
- Department of PET/CT, the First Affiliated Hospital of Xi'an Jiaotong University, Xi'an, Shaanxi, China
| | - Haining Li
- Department of PET/CT, the First Affiliated Hospital of Xi'an Jiaotong University, Xi'an, Shaanxi, China
| | - Ming Zhang
- Department of Medical Imaging, the First Affiliated Hospital of Xi'an Jiaotong University, Xi'an, Shaanxi, China.
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Surkar SM, Lin CC, Trotter B, Phinizy T, Sylcott B. Effects of dual-task training on cognitive-motor learning and cortical activation: A non-randomized clinical trial in healthy young adults. PLoS One 2025; 20:e0322036. [PMID: 40338969 PMCID: PMC12061167 DOI: 10.1371/journal.pone.0322036] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [MESH Headings] [Grants] [Track Full Text] [Download PDF] [Figures] [Journal Information] [Subscribe] [Scholar Register] [Received: 09/16/2024] [Accepted: 02/25/2025] [Indexed: 05/10/2025] Open
Abstract
Dual-task (DT) training, which involves the simultaneous execution of cognitive and motor tasks, has been shown to influence task performance and cortical activation, yet evidence on the effects of DT training and cortical activation for complex postural control tasks remains limited. This study investigated the immediate and retention effects of a one-week DT training program on DT learning, performance in DT and single-task conditions, and activation in bilateral prefrontal (PFC) and vestibular cortices in healthy young adults. Eighteen individuals (age = 22.39 ± 1.73 years) participated in the study. The DT paradigm involved a dynamic stability platform (motor task) paired with either a simple or complex auditory reaction time (RT) task (cognitive). Participants completed 20-25 minutes of DT training (18 trials/day) across five consecutive days. DT performance was measured by the duration participants maintained the stability platform within 3 degrees of the horizontal while responding to auditory stimuli. Single-task motor and cognitive performances were also assessed. Cortical activation in the PFC and vestibular cortices was measured using functional near infrared spectroscopy (fNIRS), tracking changes in oxygenated hemoglobin (HbO) concentrations. Pre-training, post-training, and one-week follow-up testing was conducted. The results demonstrate that DT training significantly improves and retains DT performance, likely due to a reduction in cognitive-motor interference. Additionally, DT training led to decreased activation in the bilateral PFC and vestibular cortices, specifically for complex DT condition, suggesting enhanced attentional resource allocation and optimized vestibular input processing, indicative of neural efficiency. Notably, these training effects also transferred to single-task cognitive and motor performances, with corresponding reductions in PFC and vestibular cortex activation, despite the lack of direct training on these tasks. This study advances our understanding of the neural mechanisms underlying DT training and underscores the critical role of practice in optimizing cognitive-motor efficiency.
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Affiliation(s)
- Swati M. Surkar
- Department of Physical Therapy, East Carolina University, Greenville, North Carolina, United States of America
| | - Chia-Cheng Lin
- Department of Physical Therapy, East Carolina University, Greenville, North Carolina, United States of America
| | - Brittany Trotter
- Department of Kinesiology, East Carolina University, Greenville, North Carolina, United States of America
| | - Tyler Phinizy
- Division of Physical Therapy, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, United States of America
| | - Brian Sylcott
- Department of Engineering, East Carolina University, Greenville, North Carolina, United States of America
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37
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Dimakou A, Pezzulo G, Zangrossi A, Corbetta M. The predictive nature of spontaneous brain activity across scales and species. Neuron 2025; 113:1310-1332. [PMID: 40101720 DOI: 10.1016/j.neuron.2025.02.009] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Track Full Text] [Journal Information] [Subscribe] [Scholar Register] [Received: 11/04/2024] [Revised: 01/30/2025] [Accepted: 02/12/2025] [Indexed: 03/20/2025]
Abstract
Emerging research suggests the brain operates as a "prediction machine," continuously anticipating sensory, motor, and cognitive outcomes. Central to this capability is the brain's spontaneous activity-ongoing internal processes independent of external stimuli. Neuroimaging and computational studies support that this activity is integral to maintaining and refining mental models of our environment, body, and behaviors, akin to generative models in computation. During rest, spontaneous activity expands the variability of potential representations, enhancing the accuracy and adaptability of these models. When performing tasks, internal models direct brain regions to anticipate sensory and motor states, optimizing performance. This review synthesizes evidence from various species, from C. elegans to humans, highlighting three key aspects of spontaneous brain activity's role in prediction: the similarity between spontaneous and task-related activity, the encoding of behavioral and interoceptive priors, and the high metabolic cost of this activity, underscoring prediction as a fundamental function of brains across species.
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Affiliation(s)
- Anastasia Dimakou
- Padova Neuroscience Center, Padova, Italy; Veneto Institute of Molecular Medicine, VIMM, Padova, Italy
| | - Giovanni Pezzulo
- Institute of Cognitive Sciences and Technologies, National Research Council, Rome, Italy
| | - Andrea Zangrossi
- Padova Neuroscience Center, Padova, Italy; Department of General Psychology, University of Padova, Padova, Italy
| | - Maurizio Corbetta
- Padova Neuroscience Center, Padova, Italy; Veneto Institute of Molecular Medicine, VIMM, Padova, Italy; Department of Neuroscience, University of Padova, Padova, Italy.
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38
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Ding L, Zhang Y, Xie Y, He Y, Wang Y, Lu J, Pang R, Wang W, Chen Z. Cortical activation and functional connectivity during different attention tasks using functional near-infrared spectroscopy in middle-aged and elderly people. Eur J Med Res 2025; 30:364. [PMID: 40325473 PMCID: PMC12054223 DOI: 10.1186/s40001-025-02597-1] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Grants] [Track Full Text] [Journal Information] [Subscribe] [Scholar Register] [Received: 01/13/2025] [Accepted: 04/14/2025] [Indexed: 05/07/2025] Open
Abstract
BACKGROUND Attention plays a vital part in the cognitive process, where different kinds of attention are associated with separate brain mechanisms. The objective of this research was to investigate the patterns of brain activation and functional connectivity in middle-aged and elderly individuals, while they were engaged in various attentional tasks, with the intention of establishing a reference foundation for the clinical treatment of attention disorders. MATERIALS AND METHODS A total of 44 healthy middle-aged and elderly persons (47.1% women) aged over 40 were enrolled in this study. The digital cancellation test (DCT), the paced auditory serial addition test (PASAT), the Stroop colour-word test, and the trail making test (TMT) are, respectively, associated with four types of attention tasks: sustained attention, divided attention, selective attention, and attention shifting. Functional near-infrared spectroscopic imaging was employed to measure the concentration of brain oxyhaemoglobin in the subjects, while they were performing these four attention tasks. RESULTS In this study, we found distinct activation patterns in brain areas, such as BA-3, BA-4, BA-6, and others. Functional connectivity analysis revealed that the frontal and right parietal lobes consistently showed higher density and strength of connections across tasks, with the PASAT task exhibiting the highest number of connections exceeding the threshold. Notably, the DCT task demonstrated significant correlations in oxygen fluctuations among several brain regions, while the TMT-B task highlighted strong functional connectivity within the bilateral frontal and parietal lobes. CONCLUSIONS This research provides evidence that middle-aged and elderly people have different brain activation and functional connectivity patterns in different attentional tasks, suggesting individualized treatment for attention disorder patients based on impairment type and location. TRIAL REGISTRATION This study has been registered through the Chinese Clinical Trial Registry (ChiCTR2400087755).
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Affiliation(s)
- Lijuan Ding
- Department of Rehabilitation, the General Hospital of Western Theater Command (Affiliated Hospital of Southwest Jiaotong University), College of Medicine, Southwest Jiaotong University, Chengdu, China
| | - Yiru Zhang
- Jinchen Rehabilitation Hospital of Chengdu, Chengdu, China
| | - Youshu Xie
- Department of Occupational Therapy, Guangdong Work Injury Rehabilitation Hospital, Guangzhou, China
| | - Yongzhi He
- North Sichuan Medical College, Nanchong, China
| | - Yunyun Wang
- Department of Rehabilitation, The Second Affiliated Hospital, Guangzhou Medical University, Guangzhou, China
| | - Jiachun Lu
- Chengdu Eighth People's Hospital (Geriatric Hospital of Chengdu Medical College), Chengdu, China
| | - Rizhao Pang
- Department of Rehabilitation, the General Hospital of Western Theater Command (Affiliated Hospital of Southwest Jiaotong University), College of Medicine, Southwest Jiaotong University, Chengdu, China
| | - Wenchun Wang
- Department of Rehabilitation, the General Hospital of Western Theater Command (Affiliated Hospital of Southwest Jiaotong University), College of Medicine, Southwest Jiaotong University, Chengdu, China.
| | - Zhesi Chen
- Department of Rehabilitation, the General Hospital of Western Theater Command (Affiliated Hospital of Southwest Jiaotong University), College of Medicine, Southwest Jiaotong University, Chengdu, China.
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39
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Du Z, Yang W, Wen X, Cai S, Liu J, Yuan K. Dysfunction and recovery of the cortical connectome gradient and its association with gene expression profiles in methamphetamine and heroin use disorders. Prog Neuropsychopharmacol Biol Psychiatry 2025; 139:111391. [PMID: 40328421 DOI: 10.1016/j.pnpbp.2025.111391] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [Track Full Text] [Journal Information] [Submit a Manuscript] [Subscribe] [Scholar Register] [Received: 01/16/2025] [Revised: 04/22/2025] [Accepted: 04/30/2025] [Indexed: 05/08/2025]
Abstract
BACKGROUND The hierarchy and segregation of community-based brain networks can be characterized by functional connectome gradient (FCG). Whether the cortical FCG was disrupted and could even be reversed after prolonged abstinence in substance use disorders (SUDs) remained unclear. Less is known about the underlying genetic basis. METHODS We utilized three independent datasets (n = 247) to investigate cortical FCG dysfunction and recovery after prolonged abstinence in methamphetamine use disorder (MUD) (n = 131), and validated in heroin use disorder (HUD) (n = 36). Furthermore, magnetic resonance spectroscopy (MRS) was employed to test the relationship between the glutamate in the ventral tegmental area (VTA) and cortical FCG. Postmortem gene expression was utilized to assess the transcriptional profiles related to cortical FCG alterations. Support vector regression (SVR) model based on the baseline cortical FCG was built to predict craving changes after long-term abstinence. RESULTS MUD and HUD individuals exhibited similar cortical FCG dysfunction and recovery at global and network levels, mainly in dorsal and ventral attentions network (DAN and VAN), frontoparietal network (FPN) and default mode network (DMN). The glutamate levels in VTA were correlated with the gradient distance between FPN and limbic network (LIM). The transcriptional profiles explained variance of the altered gradient pattern, with the most related genes enriched in synaptic signaling. Baseline cortical FCG significantly predicted craving changes after long-term abstinence. CONCLUSIONS We provided novel insights into the understanding of SUD as treatable health conditions from cortical FCG changes, which could be considered as the potential biomarkers of craving changes after prolonged abstinence for SUDs.
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Affiliation(s)
- Zhe Du
- School of Life Science and Technology, Xidian University, Xi'an, Shaanxi 710126, China
| | - Wenhan Yang
- Department of Radiology, Second Xiangya Hospital, Central South University, Changsha 410011, China.
| | - Xinwen Wen
- School of Life Science and Technology, Xidian University, Xi'an, Shaanxi 710126, China
| | - Suping Cai
- School of Life Science and Technology, Xidian University, Xi'an, Shaanxi 710126, China
| | - Jun Liu
- Department of Radiology, Second Xiangya Hospital, Central South University, Changsha 410011, China.
| | - Kai Yuan
- School of Life Science and Technology, Xidian University, Xi'an, Shaanxi 710126, China; Inner Mongolia Key Laboratory of Pattern Recognition and Intelligent Image Processing, School of Information Engineering, Inner Mongolia University of Science and Technology, Baotou, Inner Mongolia 014010, China; Engineering Research Center of Molecular and Neuro Imaging Ministry of Education, Xi'an, Shaanxi, China; Ganzhou City Key Laboratory of Mental Health, The Third People's Hospital of Ganzhou City, Ganzhou, Jiangxi, 341000, China; Xi'an Key Laboratory of Intelligent Sensing and Regulation of Trans-Scale Life Information, School of Life Science and Technology, Xidian University, Xi'an, Shaanxi 710126, China.
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40
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Gong D, Draschkow D, Nobre AC. Focusing attention in working and long-term memory through dissociable mechanisms. Nat Commun 2025; 16:4126. [PMID: 40319062 PMCID: PMC12049562 DOI: 10.1038/s41467-025-59359-0] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Grants] [Track Full Text] [Journal Information] [Subscribe] [Scholar Register] [Received: 05/12/2023] [Accepted: 04/17/2025] [Indexed: 05/07/2025] Open
Abstract
We developed an experimental approach to compare how attentional orienting facilitates retrieval from spatial working memory (WM) and long-term memory (LTM), and how selective attention within these two memory types impacts incoming sensory information processing. In three experiments with healthy young adults, retrospective attention cues prioritize an item represented in WM or LTM. Participants then retrieve a memory item or perform a perceptual task. The retrocue is informative for the retrieval task but not for the perceptual task. We show that attentional orienting benefits performance for both WM and LTM, with stronger effects for WM. Eye-tracking reveals significant gaze shifts and microsaccades correlated with attention in WM, but no statistically significant gaze biases were found for LTM. Visual discrimination of unrelated visual stimuli is consistently improved for items matching attended WM locations. Similar effects occur at LTM locations but less consistently. The findings suggest at least partly dissociable attention-orienting processes for different memory types. Although our conclusions are necessarily constrained to the type of WM and LTM representations relevant to our task, they suggest that, under certain conditions, attentional prioritization in LTM can operate independently from WM. Future research should explore whether similar dissociations extend to non-spatial or more complex forms of LTM.
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Affiliation(s)
- Dongyu Gong
- Department of Experimental Psychology, University of Oxford, Oxford, UK.
- Oxford Centre for Human Brain Activity, Wellcome Centre for Integrative Neuroimaging, Department of Psychiatry, University of Oxford, Oxford, UK.
- Department of Psychology, Yale University, New Haven, CT, USA.
| | - Dejan Draschkow
- Department of Experimental Psychology, University of Oxford, Oxford, UK.
- Oxford Centre for Human Brain Activity, Wellcome Centre for Integrative Neuroimaging, Department of Psychiatry, University of Oxford, Oxford, UK.
| | - Anna C Nobre
- Department of Experimental Psychology, University of Oxford, Oxford, UK.
- Oxford Centre for Human Brain Activity, Wellcome Centre for Integrative Neuroimaging, Department of Psychiatry, University of Oxford, Oxford, UK.
- Department of Psychology, Yale University, New Haven, CT, USA.
- Wu Tsai Institute, Yale University, New Haven, CT, USA.
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Shen C, Liu C, Chen N, Qiu A. Dedifferentiation of brain functional gradient captures cognition performance and stroke occurrence: A UK Biobank study. Neuroimage 2025; 311:121183. [PMID: 40180001 DOI: 10.1016/j.neuroimage.2025.121183] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Track Full Text] [Journal Information] [Subscribe] [Scholar Register] [Received: 08/14/2024] [Revised: 03/28/2025] [Accepted: 04/01/2025] [Indexed: 04/05/2025] Open
Abstract
Brain functional dedifferentiation, marked by reduced specificity of brain activity or greater similarity of functional connectivity (FC) among networks, is a hallmark of aging. Traditionally, task functional magnetic resonance imaging studies have explored functional dedifferentiation within specific cognitive domains, while FC-based approaches have focused on regional connectivity patterns. Here, we leverage the principal functional gradient to provide a macro-scale and integrative perspective on functional dedifferentiation in aging, offering a novel framework for understanding its relationship with aging, cognition, and disease. We utilized brain images and clinical data from the UK Biobank, comprising 23,578 participants aged 44-82. Linear regression was employed to assess relationships between the network dedifferentiation along the principal functional gradient and age, and cognitive performance across six domains in a normal aging population. We tested interactions between age, sex, and education to assess their influence on age-related dedifferentiation. Logistic regression was applied to classify stroke in participants with stroke and matched normal aging participants. Our findings revealed a reduced principal functional gradient range with age, indicating reduced FC variability of all brain regions. At the network level, the dedifferentiation between the frontoparietal and other networks was strongly linked to aging and cognitive performance. Males exhibited faster dedifferentiation than females across multiple networks. The somatomotor network was most affected by stroke-related dedifferentiation. Validation via covariate-matched subgroups confirmed the robustness of these findings. This research provides macro-scale insights into age-related brain functional changes, highlighting dedifferentiation along the principal gradient as a network-sensitive indicator of aging and the development of stroke.
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Affiliation(s)
- Chenye Shen
- Department of Biomedical Engineering, National University of Singapore, Singapore
| | - Chaoqiang Liu
- Department of Biomedical Engineering, National University of Singapore, Singapore
| | - Nanguang Chen
- Department of Biomedical Engineering, National University of Singapore, Singapore
| | - Anqi Qiu
- Department of Biomedical Engineering, National University of Singapore, Singapore; Department of Health Technology and Informatics, the Hong Kong Polytechnic University, Hong Kong; Department of Biomedical Engineering, the Johns Hopkins University, USA.
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Renton AI, Klein DJ, Livezey JA, Nemrodov D, Wolfer S, Hanina A, Van De Ville D. Video-evoked neuromarkers of visual function in age-related macular degeneration. Front Hum Neurosci 2025; 19:1569282. [PMID: 40376545 PMCID: PMC12078308 DOI: 10.3389/fnhum.2025.1569282] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [Grants] [Track Full Text] [Download PDF] [Figures] [Journal Information] [Subscribe] [Scholar Register] [Received: 01/31/2025] [Accepted: 04/10/2025] [Indexed: 05/18/2025] Open
Abstract
Neural markers of visual function in age-related macular degeneration (AMD) allow clinicians and researchers to directly evaluate the functional changes in visual processing which occur as a result of the progressive loss of afferent input from the macula. Unfortunately, few protocols exist that elicit such neural markers, and most of these are poorly adapted to AMD. Here, we propose a novel method of embedding frequency tags into full color and motion videos by periodically manipulating the contrast of visual information of different spatial frequencies at different temporal frequencies. These videos elicit steady-state visual evoked potentials (SSVEPS) in viewers which, when measured using electrophysiological neuroimaging methods, independently represent the responses of populations of neurons tuned to the tagged spatial frequencies. We used electroencephalography (EEG) to record the SSVEPs of 15 AMD patients and 16 age-matched healthy controls watching a 6-min series of natural scene videos filtered with this spatial frequency tagging method. Compared with healthy controls, AMD patients showed a lower SSVEP to high spatial frequency information, and a stronger response to the low spatial frequency information in the video set. The ratio of the SSVEP to lower relative to higher spatial frequency information was strongly predictive of both visual acuity and contrast sensitivity, and the topographic distributions of these responses suggested retinotopic reorganization of the neural response to spatial frequency information.
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Affiliation(s)
- Angela I. Renton
- Neuro-X Institute, School of Engineering, École polytechnique fédérale de Lausanne, Geneva, Switzerland
| | | | | | - Dan Nemrodov
- Dandelion Science Corp, Hoboken, NJ, United States
| | | | - Adam Hanina
- Dandelion Science Corp, Hoboken, NJ, United States
| | - Dimitri Van De Ville
- Neuro-X Institute, School of Engineering, École polytechnique fédérale de Lausanne, Geneva, Switzerland
- Department of Radiology and Medical Informatics, Faculty of Medicine, University of Geneva, Geneva, Switzerland
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Cai Y, Chen X, Guo C. AMRM: Attention-based mask reconstruction module for multi-classification of breast cancer histopathological images. Med Eng Phys 2025; 139:104335. [PMID: 40306885 DOI: 10.1016/j.medengphy.2025.104335] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Track Full Text] [Journal Information] [Subscribe] [Scholar Register] [Received: 06/04/2024] [Revised: 03/21/2025] [Accepted: 04/04/2025] [Indexed: 05/02/2025]
Abstract
Nowadays, breast cancer is a leading cause of cancer-related mortality among women globally. Approximately 10% to 15% of breast cancer patients fail to undergo timely screening, resulting in a missed opportunity for optimal treatment. Computer-aided diagnosis (CAD) systems have been used successfully in breast cancer diagnosis. Nevertheless, current systems have encountered difficulties in achieving a high degree of accuracy, with the majority of research efforts focusing on the binary classification that distinguishes benign from malignant. Different subtypes of breast cancer require different targeted therapeutic approaches. Therefore, the precise classification of the breast cancer subtype has a major impact on treatment decisions. To improve the accuracy of breast cancer multi-classification, a novel Attention-based Mask Reconstruction Module (AMRM) is proposed to improve the performance of the model. AMRM extracts features from breast cancer histopathological images through the attention module and then performs mask reconstruction to generate reconstructed features. These reconstructed features were used in a multi-classification task to accurately classify histopathological images of breast cancer. AMRM enables the network to effectively identify background and foreground in histopathological images, reduce background interference, improve adaptability to background changes, align the features extracted by the model with the pathologist's expectations, and improve classification accuracy. Results from experiments conducted on the BreakHis dataset show that the inclusion of AMRM resulted in a significant improvement in multi-classification accuracy for the AlexNet, VGG11, ResNet-50 and Data-efficient Image Transformer (DeiT) models, reaching 88.48%, 93.40%, 96.49% and 94.10% respectively. Compared to the baseline model, accuracy increased by 8.28%, 2.11%, 1.27% and 1.26% respectively, demonstrating a significant improvement.
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Affiliation(s)
- Yanguang Cai
- School of Automation, Guangdong University of Technology, Guangzhou, 511400, Guangdong, China; School of Intelligent Manufacturing and Electrical Engineering, Guangzhou Institute of Science and Technology, Guangzhou, 510540, Guangdong, China
| | - Xiang Chen
- School of Automation, Guangdong University of Technology, Guangzhou, 511400, Guangdong, China.
| | - Changle Guo
- School of Automation, Guangdong University of Technology, Guangzhou, 511400, Guangdong, China
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Zhang Q. Trait anxiety predicting the developmental trajectories of depression symptoms in children: The mediating role of attentional control. Dev Psychopathol 2025; 37:633-644. [PMID: 38439653 DOI: 10.1017/s0954579424000385] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Track Full Text] [Journal Information] [Subscribe] [Scholar Register] [Indexed: 03/06/2024]
Abstract
Trait anxiety and attentional control are important factors related to depression symptoms. The study investigated how trait anxiety and attentional control predicted the trajectories of depression symptoms during the transition into early adolescence. The mediating effect of attentional control on the relationship of trait anxiety to the trajectories of depression symptoms was also examined. Children of 9 to 10 years were recruited at Time 1. Trait anxiety, attentional control, and depression symptoms were assessed at Time 1. Depression symptoms were measured at three follow-up assessments across 18 months. Latent class growth modeling revealed high (14.4%) and low (85.6%) trajectories of depression symptoms. Higher trait anxiety and lower attentional control predicted a higher likelihood of showing the trajectory of high depressive symptoms. Attentional control mediated the relationship of trait anxiety to the trajectory membership of depression symptoms. The findings had important implications for the association of trait anxiety with the trajectory membership of depression symptoms and highlighted the importance of attentional control in the development of depression symptoms for children with high trait anxiety.
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Affiliation(s)
- Qiaochu Zhang
- Department of Social and Behavioural Sciences, College of Humanities and Social Sciences, City University of Hong Kong, Kowloon, Hong Kong
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Fujiyama H, Bowden VK, Tang AD, Tan J, Librizzi E, Loft S. Repeated application of bifocal transcranial alternating current stimulation improves network connectivity but not response inhibition: a double-blind sham control study. Cereb Cortex 2025; 35:bhaf110. [PMID: 40364567 PMCID: PMC12075771 DOI: 10.1093/cercor/bhaf110] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Grants] [Track Full Text] [Download PDF] [Figures] [Journal Information] [Subscribe] [Scholar Register] [Received: 02/07/2025] [Revised: 03/25/2025] [Accepted: 04/15/2025] [Indexed: 05/15/2025] Open
Abstract
Mounting evidence suggests that transcranial alternating current stimulation can enhance response inhibition, a cognitive process crucial for sustained effort and decision-making. However, most studies have focused on within-session effects, with limited investigation into the effects of repeated applications, which are crucial for clinical applications. We examined the effects of repeated bifocal transcranial alternating current stimulation targeting the right inferior frontal gyrus and pre-supplementary motor area on response inhibition, functional connectivity, and simulated driving performance. Thirty young adults (18-35 yr) received either a sham or transcranial alternating current stimulation (20 Hz, 20 min) across 5 sessions over 2 wk. Resting-state electroencephalography assessed functional connectivity between the pre-supplementary motor area and right inferior frontal gyrus at baseline, the final transcranial alternating current stimulation session, and the 7-d follow-up. Response inhibition was measured using a stop-signal task, and driving performance was assessed before and after the intervention. The results showed significant improvements in functional connectivity in the transcranial alternating current stimulation group between sessions, though response inhibition and driving braking performance remained unchanged. However, while not the targeted behavior, general driving performance potentially improved following bifocal transcranial alternating current stimulation, with participants maintaining stable driving behavior alongside increased spare attentional capacity. These findings suggest that repeated bifocal transcranial alternating current stimulation may enhance cortical connectivity and related cognitive-motor processes, supporting its potential for clinical applications.
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Affiliation(s)
- Hakuei Fujiyama
- School of Psychology, Murdoch University, Western Australia, 90 South Street, Murdoch, WA 6150, Australia
- Centre for Healthy Ageing, Health Futures Institute, Murdoch University, Western Australia, 90 South Street, Murdoch, WA 6150, Australia
- Personalised Medicine Centre, Health Futures Institute, Murdoch University, Western Australia, 90 South Street, Murdoch, WA 6150, Australia
| | - Vanessa K Bowden
- School of Psychological Science, The University of Western Australia, 35 Stirling Hwy, Crawley Western Australia, 6009, Australia
| | - Alexander D Tang
- Experimental and Regenerative Neurosciences, The University of Western Australia, 35 Stirling Hwy, Crawley, WA 6009, Australia
- Perron Institute for Neurological and Translational Sciences, Ground RR Block QE II Medical Centre Ralph & Patricia Sarich Neuroscience Building, 8 Verdun St, Nedlands, WA 6009, Australia
- Pharmacology and Toxicology Discipline, School of Biomedical Sciences, The University of Western Australia, 35 Stirling Hwy, Crawley Western Australia, 6009, Australia
| | - Jane Tan
- School of Psychology, Murdoch University, Western Australia, 90 South Street, Murdoch, WA 6150, Australia
- Centre for Healthy Ageing, Health Futures Institute, Murdoch University, Western Australia, 90 South Street, Murdoch, WA 6150, Australia
| | - Elisha Librizzi
- School of Psychology, Murdoch University, Western Australia, 90 South Street, Murdoch, WA 6150, Australia
| | - Shayne Loft
- School of Psychological Science, The University of Western Australia, 35 Stirling Hwy, Crawley Western Australia, 6009, Australia
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Lv L, Lin N, Gao W, Zhai F, Wang J, Xiang H, Liu X, Sun H, Lu Q, Wang M, Liu Q, Zhu Y. Differentiation with electroencephalography microstate in temporal lobe epilepsy with and without cognitive decline. Epilepsy Behav 2025; 166:110365. [PMID: 40090169 DOI: 10.1016/j.yebeh.2025.110365] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Track Full Text] [Journal Information] [Submit a Manuscript] [Subscribe] [Scholar Register] [Received: 09/13/2024] [Revised: 03/01/2025] [Accepted: 03/06/2025] [Indexed: 03/18/2025]
Abstract
OBJECTIVE Electroencephalography (EEG) microstate analysis is widely used in the study of various neurological and psychiatric disorders. We aim to assess whether EEG microstates are altered in TLE patients with and without cognitive decline. METHODS This study included a total of 47 temporal lobe epilepsy (TLE) patients with or without cognitive decline and 14 healthy controls (HCs). All participants underwent 64-channel EEG monitoring. Two-minute epochs of preprocessed eye closed awake EEG data were extracted for microstate analysis. Participants were divided into groups based on intelligence quotient (IQ) scores assessed by the Wechsler Intelligence Scale: normal cognition group (n = 23, IQ ≥ 90) and abnormal cognition group (n = 24, IQ < 90). We conducted frequency spectral analysis on each frequency sub-bands (delta, 1-4 Hz; theta, 4-8 Hz; alpha, 8-12 Hz; beta, 12-30 Hz) of the three groups. Then the following microstate parameters were extracted for analysis over the full frequency band (1-30 Hz) and frequency sub-bands: duration, coverage, occurrence, and transition probability. Statistical analysis using multivariate analysis of variance (MANOVA) with Bonferroni correction (α = 0.0025). RESULT Microstate analysis in the beta sub-band revealed significant differences among groups. TLE patients with abnormal cognition showed increased occurrence of Map-D; significantly higher transition probabilities from Map-A, Map-B, and Map-C to Map-D; and distinct microstate characteristics compared to patients with normal cognition and HCs. In frequency spectral analysis, the power across all frequency sub-bands showed no significant differences among TLE patients with normal cognition, TLE patients with abnormal cognition, and HCs. CONCLUSION Beta sub-band EEG microstates, particularly Map-D characteristics, may serve as potential neurophysiological markers for cognitive decline in TLE patients.
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Affiliation(s)
- Lingxuan Lv
- Department of Neurology, State Key Laboratory of Complex Severe and Rare Diseases, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing 100730, China
| | - Nan Lin
- Department of Neurology, State Key Laboratory of Complex Severe and Rare Diseases, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing 100730, China
| | - Weifang Gao
- Department of Neurology, State Key Laboratory of Complex Severe and Rare Diseases, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing 100730, China
| | - Feifei Zhai
- Department of Neurology, State Key Laboratory of Complex Severe and Rare Diseases, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing 100730, China
| | - Jing Wang
- Department of Neurology, SanBo Brain Hospital, Capital Medical University, Beijing 100093, China
| | - Huanhuan Xiang
- Department of Neurology, SanBo Brain Hospital, Capital Medical University, Beijing 100093, China
| | - Xinshan Liu
- Department of Neurology, SanBo Brain Hospital, Capital Medical University, Beijing 100093, China
| | - Heyang Sun
- Department of Neurology, State Key Laboratory of Complex Severe and Rare Diseases, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing 100730, China
| | - Qiang Lu
- Department of Neurology, State Key Laboratory of Complex Severe and Rare Diseases, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing 100730, China.
| | - Mengyang Wang
- Department of Neurology, SanBo Brain Hospital, Capital Medical University, Beijing 100093, China.
| | - Qing Liu
- Department of Neurology, State Key Laboratory of Complex Severe and Rare Diseases, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing 100730, China.
| | - Yicheng Zhu
- Department of Neurology, State Key Laboratory of Complex Severe and Rare Diseases, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing 100730, China
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Ma C, Li Y, Gao Y, Lin X, Hou Y, He W, Zhu Y, Jiang J, Xie Y, Fang P. Impact of working memory training on brain network integration and neurotransmitter systems: a resting-state fMRI. Cereb Cortex 2025; 35:bhaf081. [PMID: 40319377 DOI: 10.1093/cercor/bhaf081] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Grants] [Track Full Text] [Journal Information] [Subscribe] [Scholar Register] [Received: 01/14/2025] [Revised: 03/07/2025] [Accepted: 03/20/2025] [Indexed: 05/07/2025] Open
Abstract
Working memory training (WMT) has been demonstrated to enhance cognitive performance, yet the underlying neural mechanisms remain insufficiently understood. Brain network connectivity, particularly as measured by the participation coefficient (PC), offers a valuable framework for elucidating these neural changes. This study investigated the effects of WMT on brain network connectivity, utilizing PC as a primary assessment of network integration and segregation. The relationship between WMT-induced changes in PC and the density of specific neurotransmitter receptors was examined. Seventy-six healthy participants were randomly assigned to either a WMT group or a control group. After 8 wks of training, the WMT group exhibited significant cognitive improvements, especially in near and far transfer tasks. These behavioral improvements were accompanied by specific changes in brain connectivity, including a reduction in PC within the sensorimotor network and node-specific alterations in the left prefrontal cortex, temporo-occipital-parietal junction, and parietal operculum. Moreover, changes in PC were significantly correlated with the density of dopamine D2 receptors, mu-opioid receptors, and metabotropic glutamate receptor 5. These findings enhance our understanding of how WMT influences cognitive function and brain network connectivity, highlighting the potential for targeting specific networks and neurotransmitter systems in cognitive training interventions.
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Affiliation(s)
- Chaozong Ma
- Military Medical Psychology School, The Fourth Military Medical University, No. 169 Changle West Road, Xi'an 710032, Shaanxi Province, China
| | - Yijun Li
- Military Medical Psychology School, The Fourth Military Medical University, No. 169 Changle West Road, Xi'an 710032, Shaanxi Province, China
| | - Yuntao Gao
- Military Medical Psychology School, The Fourth Military Medical University, No. 169 Changle West Road, Xi'an 710032, Shaanxi Province, China
| | - Xinxin Lin
- Military Medical Psychology School, The Fourth Military Medical University, No. 169 Changle West Road, Xi'an 710032, Shaanxi Province, China
| | - Yilin Hou
- Military Medical Psychology School, The Fourth Military Medical University, No. 169 Changle West Road, Xi'an 710032, Shaanxi Province, China
| | - Wei He
- Department of Radiation Protection Medicine, Department of Military Preventive Medicine, The Fourth Military Medical University, No. 169 Changle West Road, Xi'an 710032, Shaanxi Province, China
| | - Yuanqiang Zhu
- Department of Radiology, Xijing Hospital, The Fourth Military Medical University, No. 127 Changle West Road, Xi'an 710032, Shaanxi Province, China
| | - Jun Jiang
- The Youth Innovation Team of Shaanxi University, Equipment Management and Unmanned Aerial Vehicle Engineering School, Air Force Engineering University (AFEU), No. 1, East Changle Road, Xi'an 710038, Shaanxi Province, China
| | - Yuanjun Xie
- Military Medical Psychology School, The Fourth Military Medical University, No. 169 Changle West Road, Xi'an 710032, Shaanxi Province, China
| | - Peng Fang
- Military Medical Psychology School, The Fourth Military Medical University, No. 169 Changle West Road, Xi'an 710032, Shaanxi Province, China
- The Youth Innovation Team of Shaanxi University, Equipment Management and Unmanned Aerial Vehicle Engineering School, Air Force Engineering University (AFEU), No. 1, East Changle Road, Xi'an 710038, Shaanxi Province, China
- Shaanxi Provincial Key Laboratory of Bioelectromagnetic Detection and Intelligent Perception, No. 169 Changle West Road, Xi'an 710032, Shaanxi Province, China
- Military Medical Innovation Center, The Fourth Military Medical University, No. 169 Changle West Road, Xi'an 710032, Shaanxi Province, China
- School of Biomedical Engineering, The Fourth Military Medical University, No. 169 Changle West Road, Xi'an 710032, Shaanxi Province, China
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48
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Palmer LRJ, Sumanapala DK, Mareschal D, Dumontheil I. Neural Associations between Inhibitory Control and Counterintuitive Reasoning in Science and Maths in Primary School Children. J Cogn Neurosci 2025; 37:915-940. [PMID: 39869328 DOI: 10.1162/jocn_a_02303] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [MESH Headings] [Grants] [Track Full Text] [Journal Information] [Subscribe] [Scholar Register] [Indexed: 01/28/2025]
Abstract
Emerging evidence suggests that inhibitory control (IC) plays a pivotal role in science and maths counterintuitive reasoning by suppressing incorrect intuitive concepts, allowing correct counterintuitive concepts to come to mind. Neuroimaging studies have shown greater activation in the ventrolateral and dorsolateral pFCs when adults and adolescents reason about counterintuitive concepts, which has been interpreted as reflecting IC recruitment. However, the extent to which neural systems underlying IC support science and maths reasoning remains unexplored in children. This developmental stage is of particular importance, as many crucial counterintuitive concepts are learned in formal education in middle childhood. To address this gap, fMRI data were collected while fifty-six 7- to 10-year-olds completed counterintuitive science and math problems, plus IC tasks of interference control (Animal Size Stroop) and response inhibition (go/no-go). Univariate analysis showed large regional overlap in activation between counterintuitive reasoning and interference control, with more limited activation observed in the response inhibition task. Multivariate similarity analysis, which explores fine-scale patterns of activation across voxels, revealed neural activation similarities between (i) science and maths counterintuitive reasoning and interference control tasks in frontal, parietal, and temporal regions, and (ii) maths reasoning and response inhibition tasks in the precuneus/superior parietal lobule. Extending previous research in adults and adolescents, this evidence is consistent with the proposal that IC, specifically interference control, supports children's science and maths counterintuitive reasoning, although further research will be needed to demonstrate the similarities observed do not reflect more general multidemand processes.
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Singer T. A neuroscience perspective on the plasticity of the social and relational brain. Ann N Y Acad Sci 2025; 1547:52-74. [PMID: 40178439 PMCID: PMC12096818 DOI: 10.1111/nyas.15319] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Track Full Text] [Download PDF] [Figures] [Journal Information] [Subscribe] [Scholar Register] [Indexed: 04/05/2025]
Abstract
Over the past two decades, the fields of social and contemplative neurosciences have made significant strides. Initial research utilizing fMRI identified neuronal networks involved in empathy, mentalizing, and compassion, as well as complex interactions among these networks. Subsequent studies shifted to testing the plasticity of these social skills via different types of mindfulness- or compassion-based mental training programs, demonstrating brain plasticity, enhanced social capacities and motivation, as well as improved mental health and overall well-being. Next, researchers developed scalable evidence-based online mental training programs to address the growing levels of mental health problems and loneliness, both exacerbated by the COVID-19 pandemic. Innovative approaches, such as novel relational partner-based practices and online app-based dyadic training programs, offer scalable solutions to counteract ongoing societal and mental health deterioration. Current studies are now applying the above findings to support resilience building within diverse domains of society and professional populations-such as healthcare workers and teachers-at high risk of burn-out. Future research should explore the broader impact of such training-related individual changes on larger systems, potentially leading to the development of a translational social neuroscience approach that leverages insights from social brain plasticity research to support societal needs, thereby enhancing resilience, mental health, and social cohesion.
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Affiliation(s)
- Tania Singer
- Social Neuroscience LabMax Planck SocietyBerlinGermany
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50
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Wang JW, Zhang DW, Johnstone SJ. Portable EEG for assessing attention in educational settings: A scoping review. Acta Psychol (Amst) 2025; 255:104933. [PMID: 40154053 DOI: 10.1016/j.actpsy.2025.104933] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Track Full Text] [Journal Information] [Subscribe] [Scholar Register] [Received: 08/23/2024] [Revised: 03/05/2025] [Accepted: 03/18/2025] [Indexed: 04/01/2025] Open
Abstract
BACKGROUND Portable EEG provides the opportunity to capture neural correlates of attention in a more naturalistic environment. However, the field is still in its infancy, with varied research aims and methodologies. The current scoping review aims to clarify: (1) the research aims of the studies, (2) the portable EEG collection methodologies, and (3) the EEG measures of attention. METHOD The review followed the Preferred Reporting Items for Systematic Review and Meta-Analysis - Scoping Review extension. Two authors extracted data items from 45 eligible studies. RESULTS Three research aims were identified in previous studies: examining the effects of learning-related factors on attention captured by portable EEG (n = 23), developing attention classification algorithms (n = 7) and software for monitoring and promoting attention (n = 10), and verifying the signal quality of EEG derived from portable EEG in attentional tasks (n = 5). The testing sites and tasks were predominantly out-of-lab controlled settings and structured learning materials. To quantify attention, 8 studies employed a theory-driven approach, e.g., using EEG measures based on prior research correlating specific spectral power with attention. In contrast, 37 studies used data-driven approaches, e.g., using spectral power as input features for machine learning models to index attention. DISCUSSION Portable EEG has been a promising approach to measuring attention in educational settings. Meanwhile, there are challenges and opportunities related to the better translation of cognitive neuroscience research into practice.
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Affiliation(s)
- Jian-Wei Wang
- Department of Psychology, Yangzhou University, Yangzhou, China
| | - Da-Wei Zhang
- Department of Psychology, Yangzhou University, Yangzhou, China; Department of Psychology, Monash University Malaysia, Bandar Sunway, Malaysia.
| | - Stuart J Johnstone
- School of Psychology, University of Wollongong, Wollongong, Australia; Brain Behaviour Institute, University of Wollongong, Wollongong, Australia
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