Delpino MV. Letter to the Editor: Skeletal muscle transcriptomics in metabolic dysfunction-associated steatotic liver disease - balancing promise with validation. World J Gastroenterol 2026; 32(38): 121683 [DOI: 10.3748/wjg.121683]
Corresponding Author of This Article
María Victoria Delpino, PhD, Instituto de Investigaciones Biomédicas en Retrovirus y Sida, Universidad de Buenos Aires, Consejo Nacional de Investigaciones Científicas y Técnicas, Paraguay 2155, Buenos Aires C1121ABG, Argentina. mdelpino@ffyb.uba.ar
Research Domain of This Article
Gastroenterology & Hepatology
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letter
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Delpino MV. Letter to the Editor: Skeletal muscle transcriptomics in metabolic dysfunction-associated steatotic liver disease - balancing promise with validation. World J Gastroenterol 2026; 32(38): 121683 [DOI: 10.3748/wjg.121683]
World J Gastroenterol. Oct 14, 2026; 32(38): 121683 Published online Oct 14, 2026. doi: 10.3748/wjg.121683
Letter to the Editor: Skeletal muscle transcriptomics in metabolic dysfunction-associated steatotic liver disease - balancing promise with validation
María Victoria Delpino
María Victoria Delpino, Instituto de Investigaciones Biomédicas en Retrovirus y Sida, Universidad de Buenos Aires, Consejo Nacional de Investigaciones Científicas y Técnicas, Buenos Aires C1121ABG, Argentina
Author contributions: The author solely conceived, drafted, critically revised, and approved the final version of the manuscript.
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Conflict-of-interest statement: The author reports no relevant conflicts of interest for this article.
Corresponding author: María Victoria Delpino, PhD, Instituto de Investigaciones Biomédicas en Retrovirus y Sida, Universidad de Buenos Aires, Consejo Nacional de Investigaciones Científicas y Técnicas, Paraguay 2155, Buenos Aires C1121ABG, Argentina. mdelpino@ffyb.uba.ar
Received: March 30, 2026 Revised: April 16, 2026 Accepted: May 18, 2026 Published online: October 14, 2026 Processing time: 158 Days and 23.7 Hours
Abstract
This letter underscores the clinical relevance of the study by Zhang et al published in the World Journal of Gastroenterology on exercise-responsive skeletal muscle genes in metabolic dysfunction-associated steatotic liver disease and commends its integrative design. We also note key limitations, including a permissive differential expression threshold that could be refined by applying more stringent criteria (e.g., |log2FC| ≥ 0.5 with false discovery rate < 0.05) and the fact that receiver operating characteristic analyses do not equate to clinical diagnostic validation. The exercise-related changes in LAMA4, PECAM1, PXDN, and THBS4 are intriguing and may reflect muscle-liver crosstalk; however, further human and functional validation is needed before clinical translation.
Core Tip: Zhang et al identify exercise-responsive skeletal muscle genes that may help explain the metabolic benefits of exercise in metabolic dysfunction-associated steatotic liver disease. Their integrative approach is promising, but these candidate markers require validation in well-designed, multi-center prospective human cohorts with paired liver histology or imaging data, additional human validation and functional studies before they can be considered for clinical use.