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World J Clin Pediatr. May 8, 2018; 7(2): 67-74
Published online May 8, 2018. doi: 10.5409/wjcp.v7.i2.67
Is obesity related to the lung function of non-asthmatic children?
Andrew Fretzayas, School of Medicine, University of Athens, Athens 11527, Greece
Andrew Fretzayas, Department of Pediatrics, Athens Medical Center, Athens University Medical School, Maroussi 15125, Greece
Maria Moustaki, Ioanna Loukou, Department of Cystic Fibrosis, “Agia Sofia”, Children’s Hospital, Athens 11527, Greece
Konstantinos Douros, Respiratory Unit, Third Department of Pediatrics, Athens University Medical School, “Attikon” University Hospital, Haidari 15125, Greece
ORCID number: Andrew Fretzayas (0000-0003-0964-8594); Maria Moustaki (0000-0001-6818-4350); Ioanna Loukou (0000-0002-3617-4526); Konstantinos Douros (0000-0001-7632-1159).
Author contributions: All authors contributed equally to this paper.
Conflict-of-interest statement: Dr. Moustaki has nothing to disclose.
Open-Access: This article is an open-access article which was selected by an in-house editor and fully peer-reviewed by external reviewers. It is distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/
Correspondence to: Andrew Fretzayas, MD, PhD, Professor of Pediatrics, Department of Pediatrics, Athens Medical Center, Athens University Medical School, 5-7 Distomou Str, Maroussi 15125, Greece. afretz@med.uoa.gr
Telephone: +30-210-6157269 Fax: +30-210-6862376
Received: February 12, 2018
Peer-review started: February 12, 2018
First decision: March 2, 2018
Revised: March 12, 2018
Accepted: April 11, 2018
Article in press: April 11, 2018
Published online: May 8, 2018

Abstract

Overweight and obesity are highly prevalent in developed and developing countries among children and adolescents. During the last two decades, it became evident that excess weight is adversely related to respiratory health in childhood and adolescence mainly in terms of asthma occurrence. Additionally, there is a mounting body of evidence that overweight/obesity may also affect lung function in non-asthmatic subjects. The aim of this review was to present and discuss the studies that investigated this issue in non-asthmatic children and adolescents. Only a few studies have evaluated the impact of excess weight on static volumes and their results point towards an inverse relationship between overweight/obesity and functional residual capacity. More studies have been conducted on the impact of excess weight on dynamic lung volumes with inconsistent, however, results. Nevertheless, a relatively consistent finding was that the ratio of forced expiratory volume in 1 s/forced vital capacity was significantly lower among overweight/obese children compared to their counterparts with normal weight. The underlying mechanisms of these observations have not been adequately elucidated but it is believed to result from complex interaction of mechanical, developmental, and metabolic causes. There is a need for more well-designed studies in order to clarify the impact of excess weight on lung function in non-asthmatic subjects, as well as to explore the contribution of factors such as duration and degree of obesity, and fat distribution. Despite the absence of conclusive data, there are still convincing evidence to be communicated to the children and their families as part of the arguments to encourage them to adopt a healthier lifestyle.

Key Words: Obesity, Lung function, Spirometry, Lung volumes, Plethysmography

Core tip: We herein present an overview of the existing studies regarding the influence of excess weight on static and dynamic volumes of lung function in otherwise healthy children and adolescents. Although the existing data, are to some extent, conflicting, it seems that in this age group, obesity is correlated to a significant, though not necessarily clinically important, decrease of forced expiratory volume in 1 s/forced vital capacity ratio and a reduction of functional residual capacity. These observations are of clinical relevance, as they may be the origin of respiratory problems in adulthood, especially if obesity persists till then.



INTRODUCTION

There is sufficient data indicating that the prevalence of overweight and obesity among children and adolescents is substantial, particularly in industrialized countries. In a recent global pooled analysis, it was found that the mean body mass index (BMI) and the prevalence of obesity have increased worldwide in children and adolescents over the last four decades[1]. This rising trend has attenuated or even plateaued-albeit at high levels-in high income countries, since the end of the previous century. On the contrary, the rising still continues in middle and low income countries[2]. The high prevalence of overweight and obesity is of utmost importance for public health; the increased BMI in childhood and adolescence enhances substantially the likelihood of overweight or obesity persistence in adulthood[3] and so, the adverse health effects are not restricted to children. The most extensively studied health effects of overweight and obesity in adulthood involve cardiovascular diseases and cancer[4]. However, it has become more than obvious that obesity is also associated with respiratory health through various pathophysiologic pathways[5] and can affect lung function even in otherwise healthy subjects[5].

The aim of this review is to present the existing data on the impact of obesity in plythesmographic and spiromentic indices of pulmonary function of otherwise healthy children. The implications of the relevant observations would also be discussed.

DEFINITION OF OBESITY

Different expert committees have advocated the use of BMI as a convenient tool with acceptable reliability for the screening of obesity in children aged 2-18 years[6]. In particular, BMI ≥ 95th percentile for age has been defined as obesity whereas BMI ≥ 85Th and < 95th percentile for age as overweight[7]. The majority of studies that investigated the association of obesity with lung function in childhood and adolescence used BMI as an indicator of obesity. However, in some studies researchers preferred to use waist circumference percentiles (WCP) because this index is believed to reflect more accurately the amount of visceral adipose tissue[6]. The results of all relevant studies will be presented here, irrespective of the tool that was used for the definition of obesity.

IMPACT OF OVERWEIGHT-OBESITY ON PLETHYSMOGRAPHIC INDICES OF LUNG FUNCTION (STATIC LUNG VOLUMES)

PubMed was searched from January 1997 till the end of October 2017. Only articles in English language were eligible. Five studies were identified that had investigated the impact of overweight/obesity on the plethysmographic indices of lung function in children and adolescents. A summary of these studies is presented in Table 1, in chronological order. The relationship of BMI with total lung capacity (TLC) was investigated by all researchers without finding any significant association. The only exception was the study of van de Griendt et al[8] who did not simply assessed the relationship of BMI with TLC but rather tried to explore the effect of BMI reduction on lung volumes after an intervention program of weight reduction. The % predicted TLC increased by 2.27% (0.86%-3.86%) after weight loss and this increase was statistically significant. Nevertheless, the population of this study was consisted of extremely obese children with either a BMI equivalent ≥ 35 kg/m2, or a BMI equivalent to at least 30 kg/m2 plus a comorbidity related to obesity; as a consequence, it is questionable whether generalization of the study findings is proper or not. Quite similarly, however, in the study of Li et al[9], and despite the absence of any association between BMI and TLC, there was a significant inverse correlation between trunk and subtotal body fat with TLC. Kongkiattikul et al[10], who also explored the association of trunk or body fat percentage with lung volumes, presented only data regarding functional residual capacity (FRC), and no information was given for TLC.

Table 1 Summary of studies that investigated the impact of overweight/obesity on the plethysmographic indices of lung function.
No.Ref.No. of children, age range (yr)Exclusion criteria for the study populationObesity indicesPlethysmographic variables
1Li et al[9], 200364, 7-18Children with chronic cardiorespiratory problemsBMI, Trunk Body Fat, and Subtotal Body Fat (total-head). The last 2 indices were calculated as a percentage of body massTLC, RV, FRC
2van de Griendt et al[8], 2012112, 8.5-18.9Children diagnosed as asthmaticsBM, WCTLC, ERV
3Davidson et al[12], 2014327, 6-17Children diagnosed as asthmaticsBMITLC, RV, FRC, ERV, VC
4Rastogi et al[11], 2014168, 13-18History of smoking or chronic inflammatory conditionsBMI, WC, Waist-hip ratioTLC, RV, FRC, RV/TLC, ERV, IC
5Kongkiattikul et al[10], 201545, 8.6-17.3Children with an underlying pulmonary diseaseBMI, WC, WHR Hip circumference Body fat percentage Truncal fat percentage Fat mass index Fat free mass indexTLC, RV, FRC, RV/TLC (only results for FRC were presented)

Four studies presented data for FRC and showed either significantly lower FRC levels in subjects with adiposity or, similarly, a statistically significant inverse association between FRC and adiposity. BMI was the index of adiposity in three of these studies whereas Li et al[9] found an inverse association between FRC and trunk or subtotal body fat but not with BMI. From the studies that presented data for expiratory reserve volume (ERV) and residual volume (RV)[11,12], it seems that both ERV and RV decreased with increased adiposity. ERV also increased on an average of 15% in severely obese individuals who lost weight following an intervention program[8].

IMPACT OF OVERWEIGHT-OBESITY ON SPIROMETRIC INDICES OF LUNG FUNCTION

Table 2 depicts the summary of the studies that investigated the relationship of overweight/obesity in children and/or adolescents with the spirometric variables of lung function. Twenty-three relevant studies were identified by searching PubMed from January 1997 till October 2017. Only articles in English language were eligible.

Table 2 Summary of studies that investigated the impact of overweight/obesity on spirometric indices of lung function.
No.Ref.Obesity indicesStudy populationMain findings
1Lazarus et al[34], 1997Total body fat calculated from equations based on skinfold thicknessRepresentative sample of 2464 Australian school children aged 9, 12, and 15 yoTotal body fat was inversely associated with FVC and FEV1 after adjusting for height and weight
2Li et al[9], 2003Trunk and subtotal (total-head) body fat massSixty-four obese children, 7-18 yo without cardiorespiratory problems.No significant associations between the obesity and the spirometric indices
3Perez-Padilla et al[35], 2006Trunk body fatA cross-sectional study of 6784 students 6-20 yoIn children < 11 yr FEV1 and FVC increased with BMI. In subjects > 12 yr lung function increased with BMI, reached a plateau (at a BMI Z score of 1SD) and then decreased among those with highest BMI
4Nageswari et al[36], 2007% body massTwenty obese/overweight children and 20 normal-weight (controls), 12-16 yoFEV1, FVC, FEF25%-75% were significantly lower in the obese group compared to the controls
5Chen et al[18], 2009Subtotal body fat (total-head)A cross-sectional study of 718 children 6-17 yoWC, but not BMI, was positively associated with FEV1 and FVC, and negatively associated with FEV1/FVC
6Spathopoulos et al[37], 2009% body massThree hundred fifty-seven overweight, 300 obese, and 196 normal-weight children. Not well-controlled asthma cases were excludedAll spirometric parameters were significantly different across the three groups. BMI > 85th centile was a significant independent predictor of reduced spirometric parameters after controlling for confounders
7Cibella et al[16], 2011BMICross-sectional study carried out in a sample of 708 children 10-16 yoFEV1 and FVC were lower in children with BMI > 85th centile compared to those with normal BMI. No difference was found for FEF25%-75%, FEV1/FVC
8Feng et al[19], 2012BMIA cross-sectional performed on 1572 healthy children 9-18 yo. Children with asthma were excludedWC was inversely associated with FEV1, FVC and FEV1/FVC. BMI was positively related with FEV1 and FVC and negatively associated with FEV1/FVC
9van de Griendt et al[8], 2012BMIOne hundred twelve obese children 8.5-18.9 yo, taking part in a multidisciplinary treatment programme.FEV1 and FVC increased by 2.91% and 3.08% after weight reduction following a 6 mo intervention program and this increase was significant. No significant change was observed in MEF50
10Paralikar et al[38], 2012WCThirty obese boys 12-17 yo and 30 age-matched normal-weight boysFEV1, FEV1/FVC and MVV were significantly decreased in the obese group
11Bekkers et al[20], 2013BMI, WCChildren from a birth cohort (n = 1058) examined at the age of 8 yoLarge WC in girls was associated with lower FEV1 /FVC ratio
12Davidson et al[12], 2013BMIThree hundred twenty-seven children 6-17 yo referred for lung testing due to various respiratory problems. Individuals with cardiopulmonary, chest wall disease, or asthma, were excludedPositive relationship between BMI z-score and percent predicted FVC, and VC. Negative relationship between BMI z-score and FRC, ERV, RV, and FEV1/FVC
13Han et al[17], 2014BMI, PBF, WCCross-sectional study in 2681 children 6-17 yoAmong children without asthma, BMI, PBF, and WC were associated with higher FEV1 and FVC, and lower FEV1/FVC
14Khan et al[39], 2014BMI, WC, WHR, skinfold measurementsA sample of 1583 children, < 18 yo. No data on asthma diagnosis was providedOverweight/obese boys, had WC and WHR inversely associated with residual FVC, FEV0.75, and FEV1
15Rastogi et al[11], 2014BMIA sample of 168 adolescents, 13-18 yo, irrespective of asthma statusObese adolescents had lower RV, RV/TLC ratio, ERV, and FRC, and higher IC adolescents; the 2 groups did not differ in measures of lower airway obstruction, namely FEV1/FVC, and MEF
16Torun et al[40], 2014BMIA cross-sectional study of 30 overweight, 34 obese and 64 morbidly obese children, 9-17 yo, referred to a paediatric endocrinology dept. Asthmatic patients were excluded from the studyPEF and FEV25–75 were significantly reduced in in the overweight, obese and morbidly obese children
17Bekkers et al[41], 2015BMI, WCChildren from a birth cohort examined at the ages of 8 yo (n = 1090) and 12 yo (n = 1288)At 8 yo, large WC was associated with lower FEV1/FVC after adjusting for BMI (only in girls)
18Kongkiattikul et al[10], 2015BMI, FMI, body fat percentage, truncal fat percentage, mean fat free mass indexForty-five obese children, 8-18 yoNegative correlation between FRC and almost all obesity indices
19Cibella et al[14], 2015BMIA cross-sectional study of 2393 healthy children 10-17 yo. Children with asthma were excludedFVC and FEV1 were positively but disproportionately correlated to weight. FEV1/FVC and FEF25-75%/FVC ratios were negatively correlated to weight
20Costa Junior et al[42], 2016BMI, WC, body composition (tetrapolar bioimpedance)A cross-sectional study of 40 obese and 35 normal-weight children, 6-10 yo. Children with respiratory problems were excludedObese children had lower FEV1 and FEV1/FVC
21Liyanage et al[13], 2016BMIA cross-sectional study of 55 obese and 220 normal-weight children, 9-15 yo. Children with asthma were excludedNo significant difference in spirometric values
22Akin et al[43], 2017BMI, WC, neck circumferenceA cross-sectional study of 178 children, 5 to 15 yo. Children with asthma were excludedNegative correlation between FEV1, FEV1/FVC, and obesity indices
23Yao et al[15], 2017BMI1717 children, 5 to 18 yo, irrespective of asthma statusBMI is associated positively with FVC, FEV1, and PEF, and FEF25-75, but negatively with FEV1/FVC

As a general remark, the findings of these 23 studies are, to some extent, inconsistent. In 3 of the studies[9], which are discussed in the rest of the present paragraph, no difference was found in forced expiratory volume in 1 s (FEV1), forced vital capacity (FVC), FV1/FVC and FEF25%-75% between obese and/or overweight and normal-weight children. Li et al did not find an association between BMI and other adiposity indices with spirometric variables within a group of obese subjects. The study, however, did not include either overweight or normal weight individuals to serve as controls. Taking, therefore, into consideration the small sample size and the limited variation of BMI, as all subjects had BMI > 95th centile, it is likely that this study may have not had the power to detect significant associations between BMI and spirometric parameters. Liyanage et al[13] also did not find any difference when they compared overweight and obese with normal weight children. However, because the former two categories constituted one group the effect of more severe obesity on dynamic lung volumes may have been missed. Similarly, Rastogi et al[11] did not find any association between BMI or waist circumference and spirometric variables. However, asthma was neither an exclusion criterion for participants recruitment nor was taken into account in the final analysis. Accordingly, definitive conclusions cannot be drawn from this study for non-asthmatic adolescents. Kongkiattikul et al[10], who measured static as well as dynamic volumes, mentioned only the statistical significance that observed for FRC. It could therefore be hypothesized that no difference of spirometric variables was identified among the studied subjects in relation to the degree of their adiposity.

Twenty out of 23 studies revealed statistical association between the degree of adiposity and at least one of the spirometric variables. In general, the results depict a trend of significantly decreased spirometric values in the individuals at higher BMI centiles. Interestingly, however, a number of these studies revealed results that were not so clear-cut and implied a more complex association between obesity and lung function; these particular studies are discussed in some details in the following lines[14,15]. Yao et al[15] recruited obese children irrespective of asthma status. Nevertheless, in their analysis they controlled for physician-diagnosed asthma and found that excess weight was positively and significantly associated with FEV1, FVC, and FEF25%-75%, but negatively and significantly associated with FEV1/FVC. In order to interpret these findings they commented that the lower FEV1/FVC ratio in relation to higher FEV1 and FVC indicated that the lung volumes were larger in obese subjects but the airways size has not grown proportionately. Quite similar results were found in another recent study by Cibella et al[14] who also analyzed their data after controlling for age, and showed that the effect of excess weight on spirometric values was independent of age. It is worth mentioning that the results of a precedent study from the same research group in 2011[16] did not point to the same direction. However, the results of these two studies are not comparable since the population of the 2011 study included both asthmatic and non-asthmatic subjects without taking into account for asthma status. The study that first described this distinct trend of associations between adiposity indices and spirometric variables was that of Han et al[17] in 2014 which was, however, designed to explore the association of obesity indices and asthma. It is very interesting that the finding of significantly lower FEV1/FVC ratio in obese/overweight subjects has not been exclusively observed in the afore-mentioned studies; it is almost universally present among the rest of the presented studies.

The results quite often varied in studies[18,19] that used different surrogates of obesity (BMI or WC). This discrepancy indicates that adiposity markers are not necessarily interchangeable at least as far it concerns studies exploring the variations of lung function variables. Furthermore, it seems that the population age span may have affected the results of the studies to some extent. As it was shown in the PIAMA birth cohort study[20], significantly lower FEV1/FVC was observed in the whole study population, regardless of gender, at the age of 12 years but not at the age of 8 years. Therefore cross sectional studies that included children between 6-18 years may have resulted in different findings depending on the number of subjects in each specific age sub-group.

DISCUSSION

The above presented findings, despite a degree of inconsistency, indicate that the excess weight in childhood and adolescence has an adverse influence on the lung function of otherwise healthy subjects. A recent meta-analysis[21] that evaluated the effects of overweight/obesity in both children and adults found that lung function is detrimentally affected but its pattern differs between adults and children. Based on the data of the included studies, authors showed that the FEV1/FVC ratio was lower in obese/overweight children with a decrement of 2.4%. They did not find a significant difference for FEV1 or FVC. However, these conclusions were reached through a pooled analysis in asthmatic and non-asthmatic children and without having controlled for asthma status within the childhood population.

There are several factors that could have attributed to the relatively diverse findings of the studies we included in the present systematic review. The sample size employed was small in some of them; in others, the age range of the recruited participants was fairly wide and no age groups for sub-analysis were specified; not all studies excluded children with asthma diagnosis; there was not available information on the duration of the overweight/obesity, a variable that may also have an impact on lung function[22]. The variation of obesity prevalence among the different populations, as well as the type of fat deposition which was not taken into account in the majority of the studies, may also have contributed to the observed discordance of the results among some of the studies. A factor not to be overlooked is that studied populations were of different ethnicity, and it is known that the amount of visceral adiposity tissue is dependent on ethnic origin[23]. Lastly, data for maturity stage (Tanner stage) were not provided in any of the studies and therefore no adjustment was made for this parameter.

The physiologic mechanisms that underlie the impact of obesity on lung function are not entirely understood. It seems that the thoracic and abdominal fat deposition limit the outward movement of the chest wall and the descent of the diaphragm[24]. Additionally, obesity is associated with reduced compliance of the respiratory system although it is not clarified whether both lung and chest wall compliance are reduced or not[24,25]. It is also of note that obesity may coexist with obstructive sleep apnea syndrome (OSAS).Obese children have a 4.5 fold increased risk for OSAS[26] a syndrome that may further contribute to hypoventilation in obesity[27]. More recent studies suggest that the adverse effects of obesity on lung function are due not only to mechanical reasons but also to the metabolic abnormalities encountered in obesity. Rastogi et al[11] found that insulin resistance was a significant determinant of FEV1/FVC ratio and ERV in adolescents, even after adjusting for general and truncal adiposity. The above are supported from the results of a recent study conducted in obese women[28]. Additionally hepatic steatosis is more prevalent in obese children and as it was recently shown in adult population hepatic steatosis was associated with poor pulmonary function[29]. The main proposed mechanisms underlying reduced lung function in obese children are depicted in Figure 1.

Figure 1
Figure 1 Mechanisms underlying reduced lung function in obese children. ERV: Expiratory reserve volume; FEV1: Forced expiratory volume in 1 s; FVC: Forced vital capacity.

Another interesting aspect on this issue was proposed by Forno et al[30] who have shown in a recent study that obesity was related to dysanapsis. The notion of dysanaptic growth of the lung was first introduced by Green et al[31] in 1974 and it indicates a normal but disproportionate growth of the airways and parenchyma so as large lungs to be accompanied by airways with incommensurate small proportions[31,32]. In spirometry airway dysanapsis is indicated by normal FEV1 (above the 5th centile), normal high FVC (above the 75th centile), and low FEV1/FVC ratio (< 0.8)[38]. Forno et al[30] used the data of six different cohorts and analyzed them cross-sectionally - or longitudinally if that was feasible - and found that obesity was associated with dysanapsis in childhood and adolescence.

In the majority of studies the lung function values of overweight/obese children were within normal limits, and so, it could be argued that the impairment of lung function is of no clinical relevance. This may seem plausible while the subjects are at rest but it would not be likely in the case of exercise tolerance. It should be kept in mind that obesity is not only a consequence of sedentary life style but also that the physical performance of obese subjects may be lower. The latter may be due in part to the altered lung function that leads to a vicious cycle of inadequate physical activity and obesity persistence. Additionally, the persistence of overweight/obesity to adulthood may also adversely affect their lung function as adults[22,33].

As obesity is a worldwide public health problem, its adverse impact on lung function of non-asthmatic children and adolescents is of utmost importance since it may contribute to the increased morbidity of obese subjects. The physicians should be aware of this aspect of obesity and communicate this information to children and their families.

Footnotes

Manuscript source: Invited manuscript

Specialty type: Pediatrics

Country of origin: Greece

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P- Reviewer: Arslan N, Tarantino G S- Editor: Ji FF L- Editor: Filipodia E- Editor: Tan WW

References
1.  NCD Risk Factor Collaboration (NCD-RisC). Worldwide trends in body-mass index, underweight, overweight, and obesity from 1975 to 2016: a pooled analysis of 2416 population-based measurement studies in 128·9 million children, adolescents, and adults. Lancet. 2017;390:2627-2642.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 4037]  [Cited by in F6Publishing: 3623]  [Article Influence: 517.6]  [Reference Citation Analysis (0)]
2.  Ng M, Fleming T, Robinson M, Thomson B, Graetz N, Margono C, Mullany EC, Biryukov S, Abbafati C, Abera SF. Global, regional, and national prevalence of overweight and obesity in children and adults during 1980-2013: a systematic analysis for the Global Burden of Disease Study 2013. Lancet. 2014;384:766-781.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 7951]  [Cited by in F6Publishing: 7548]  [Article Influence: 754.8]  [Reference Citation Analysis (0)]
3.  Singh AS, Mulder C, Twisk JW, van Mechelen W, Chinapaw MJ. Tracking of childhood overweight into adulthood: a systematic review of the literature. Obes Rev. 2008;9:474-488.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 1656]  [Cited by in F6Publishing: 1640]  [Article Influence: 102.5]  [Reference Citation Analysis (0)]
4.  GBD 2015 Obesity Collaborators, Afshin A, Forouzanfar MH, Reitsma MB, Sur P, Estep K, Lee A, Marczak L, Mokdad AH, Moradi-Lakeh M, Naghavi M, Salama JS, Vos T, Abate KH, Abbafati C, Ahmed MB, Al-Aly Z, Alkerwi A, Al-Raddadi R, Amare AT, Amberbir A, Amegah AK, Amini E, Amrock SM, Anjana RM, Ärnlöv J, Asayesh H, Banerjee A, Barac A, Baye E, Bennett DA, Beyene AS, Biadgilign S, Biryukov S, Bjertness E, Boneya DJ, Campos-Nonato I, Carrero JJ, Cecilio P, Cercy K, Ciobanu LG, Cornaby L, Damtew SA, Dandona L, Dandona R, Dharmaratne SD, Duncan BB, Eshrati B, Esteghamati A, Feigin VL, Fernandes JC, Fürst T, Gebrehiwot TT, Gold A, Gona PN, Goto A, Habtewold TD, Hadush KT, Hafezi-Nejad N, Hay SI, Horino M, Islami F, Kamal R, Kasaeian A, Katikireddi SV, Kengne AP, Kesavachandran CN, Khader YS, Khang YH, Khubchandani J, Kim D, Kim YJ, Kinfu Y, Kosen S, Ku T, Defo BK, Kumar GA, Larson HJ, Leinsalu M, Liang X, Lim SS, Liu P, Lopez AD, Lozano R, Majeed A, Malekzadeh R, Malta DC, Mazidi M, McAlinden C, McGarvey ST, Mengistu DT, Mensah GA, Mensink GBM, Mezgebe HB, Mirrakhimov EM, Mueller UO, Noubiap JJ, Obermeyer CM, Ogbo FA, Owolabi MO, Patton GC, Pourmalek F, Qorbani M, Rafay A, Rai RK, Ranabhat CL, Reinig N, Safiri S, Salomon JA, Sanabria JR, Santos IS, Sartorius B, Sawhney M, Schmidhuber J, Schutte AE, Schmidt MI, Sepanlou SG, Shamsizadeh M, Sheikhbahaei S, Shin MJ, Shiri R, Shiue I, Roba HS, Silva DAS, Silverberg JI, Singh JA, Stranges S, Swaminathan S, Tabarés-Seisdedos R, Tadese F, Tedla BA, Tegegne BS, Terkawi AS, Thakur JS, Tonelli M, Topor-Madry R, Tyrovolas S, Ukwaja KN, Uthman OA, Vaezghasemi M, Vasankari T, Vlassov VV, Vollset SE, Weiderpass E, Werdecker A, Wesana J, Westerman R, Yano Y, Yonemoto N, Yonga G, Zaidi Z, Zenebe ZM, Zipkin B, Murray CJL. Health Effects of Overweight and Obesity in 195 Countries over 25 Years. N Engl J Med. 2017;377:13-27.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 3869]  [Cited by in F6Publishing: 4184]  [Article Influence: 597.7]  [Reference Citation Analysis (2)]
5.  Peters U, Suratt BT, Bates JHT, Dixon AE. Beyond BMI: Obesity and Lung Disease. Chest. 2018;153:702-709.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 52]  [Cited by in F6Publishing: 49]  [Article Influence: 7.0]  [Reference Citation Analysis (0)]
6.  Krebs NF, Himes JH, Jacobson D, Nicklas TA, Guilday P, Styne D. Assessment of child and adolescent overweight and obesity. Pediatrics. 2007;120 Suppl 4:S193-S228.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 585]  [Cited by in F6Publishing: 551]  [Article Influence: 32.4]  [Reference Citation Analysis (0)]
7.  Ogden CL, Flegal KM. Changes in terminology for childhood overweight and obesity. Natl Health Stat Report. 2010;1-5.  [PubMed]  [DOI]  [Cited in This Article: ]
8.  van de Griendt EJ, van der Baan-Slootweg OH, van Essen-Zandvliet EE, van der Palen J, Tamminga-Smeulders CL, Benninga MA, van Aalderen WM. Gain in lung function after weight reduction in severely obese children. Arch Dis Child. 2012;97:1039-1042.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 14]  [Cited by in F6Publishing: 14]  [Article Influence: 1.2]  [Reference Citation Analysis (0)]
9.  Li AM, Chan D, Wong E, Yin J, Nelson EA, Fok TF. The effects of obesity on pulmonary function. Arch Dis Child. 2003;88:361-363.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 151]  [Cited by in F6Publishing: 158]  [Article Influence: 7.5]  [Reference Citation Analysis (0)]
10.  Kongkiattikul L, Sritippayawan S, Chomtho S, Deerojanawong J, Prapphal N. Relationship between Obesity Indices and Pulmonary Function Parameters in Obese Thai Children and Adolescents. Indian J Pediatr. 2015;82:1112-1116.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 12]  [Cited by in F6Publishing: 9]  [Article Influence: 1.0]  [Reference Citation Analysis (0)]
11.  Rastogi D, Bhalani K, Hall CB, Isasi CR. Association of pulmonary function with adiposity and metabolic abnormalities in urban minority adolescents. Ann Am Thorac Soc. 2014;11:744-752.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 38]  [Cited by in F6Publishing: 38]  [Article Influence: 4.2]  [Reference Citation Analysis (0)]
12.  Davidson WJ, Mackenzie-Rife KA, Witmans MB, Montgomery MD, Ball GD, Egbogah S, Eves ND. Obesity negatively impacts lung function in children and adolescents. Pediatr Pulmonol. 2014;49:1003-1010.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 72]  [Cited by in F6Publishing: 75]  [Article Influence: 7.5]  [Reference Citation Analysis (0)]
13.  Liyanage G, Jayamanne B D, Aaqiff M, Sriwardhana D. Effect of body mass index on pulmonary function in children. Ceylon Med J. 2016;61:163-166.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 5]  [Cited by in F6Publishing: 6]  [Article Influence: 0.8]  [Reference Citation Analysis (0)]
14.  Cibella F, Bruno A, Cuttitta G, Bucchieri S, Melis MR, De Cantis S, La Grutta S, Viegi G. An elevated body mass index increases lung volume but reduces airflow in Italian schoolchildren. PLoS One. 2015;10:e0127154.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 27]  [Cited by in F6Publishing: 24]  [Article Influence: 2.7]  [Reference Citation Analysis (0)]
15.  Yao TC, Tsai HJ, Chang SW, Chung RH, Hsu JY, Tsai MH, Liao SL, Hua MC, Lai SH, Chen LC, Yeh KW, Tseng YL, Lin WC, Chang SC, Huang JL; Prediction of Allergies in Taiwanese Children (PATCH) Study Group. Obesity disproportionately impacts lung volumes, airflow and exhaled nitric oxide in children. PLoS One. 2017;12:e0174691.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 31]  [Cited by in F6Publishing: 34]  [Article Influence: 4.9]  [Reference Citation Analysis (0)]
16.  Cibella F, Cuttitta G, La Grutta S, Melis MR, Bucchieri S, Viegi G. A cross-sectional study assessing the relationship between BMI, asthma, atopy, and eNO among schoolchildren. Ann Allergy Asthma Immunol. 2011;107:330-336.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 40]  [Cited by in F6Publishing: 41]  [Article Influence: 3.2]  [Reference Citation Analysis (0)]
17.  Han YY, Forno E, Celedón JC. Adiposity, fractional exhaled nitric oxide, and asthma in U.S. children. Am J Respir Crit Care Med. 2014;190:32-39.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 64]  [Cited by in F6Publishing: 66]  [Article Influence: 6.6]  [Reference Citation Analysis (0)]
18.  Chen Y, Rennie D, Cormier Y, Dosman JA. Waist circumference associated with pulmonary function in children. Pediatr Pulmonol. 2009;44:216-221.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 46]  [Cited by in F6Publishing: 48]  [Article Influence: 3.2]  [Reference Citation Analysis (0)]
19.  Feng K, Chen L, Han SM, Zhu GJ. Ratio of waist circumference to chest circumference is inversely associated with lung function in Chinese children and adolescents. Respirology. 2012;17:1114-1118.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 9]  [Cited by in F6Publishing: 10]  [Article Influence: 0.9]  [Reference Citation Analysis (0)]
20.  Bekkers MB, Wijga AH, de Jongste JC, Kerkhof M, Postma D, Gehring U, Smit HA, Brunekreef B. Waist circumference, BMI, and lung function in 8-year-old children: the PIAMA birth cohort study. Pediatr Pulmonol. 2013;48:674-682.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 12]  [Cited by in F6Publishing: 14]  [Article Influence: 1.3]  [Reference Citation Analysis (0)]
21.  Forno E, Han YY, Mullen J, Celedón JC. Overweight, Obesity, and Lung Function in Children and Adults-A Meta-analysis. J Allergy Clin Immunol Pract. 2018;6:570-581.e10.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 134]  [Cited by in F6Publishing: 130]  [Article Influence: 21.7]  [Reference Citation Analysis (0)]
22.  Santamaria F, Montella S, Greco L, Valerio G, Franzese A, Maniscalco M, Fiorentino G, Peroni D, Pietrobelli A, De Stefano S. Obesity duration is associated to pulmonary function impairment in obese subjects. Obesity (Silver Spring). 2011;19:1623-1628.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 45]  [Cited by in F6Publishing: 47]  [Article Influence: 3.6]  [Reference Citation Analysis (0)]
23.  Lear SA, Humphries KH, Kohli S, Chockalingam A, Frohlich JJ, Birmingham CL. Visceral adipose tissue accumulation differs according to ethnic background: results of the Multicultural Community Health Assessment Trial (M-CHAT). Am J Clin Nutr. 2007;86:353-359.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 401]  [Cited by in F6Publishing: 401]  [Article Influence: 23.6]  [Reference Citation Analysis (0)]
24.  Robinson PD. Obesity and its impact on the respiratory system. Paediatr Respir Rev. 2014;15:219-226.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 9]  [Cited by in F6Publishing: 15]  [Article Influence: 1.5]  [Reference Citation Analysis (0)]
25.  Parameswaran K, Todd DC, Soth M. Altered respiratory physiology in obesity. Can Respir J. 2006;13:203-210.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 291]  [Cited by in F6Publishing: 289]  [Article Influence: 16.1]  [Reference Citation Analysis (0)]
26.  Redline S, Tishler PV, Schluchter M, Aylor J, Clark K, Graham G. Risk factors for sleep-disordered breathing in children. Associations with obesity, race, and respiratory problems. Am J Respir Crit Care Med. 1999;159:1527-1532.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 813]  [Cited by in F6Publishing: 750]  [Article Influence: 30.0]  [Reference Citation Analysis (0)]
27.  Arens R, Muzumdar H. Childhood obesity and obstructive sleep apnea syndrome. J Appl Physiol (1985). 2010;108:436-444.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 131]  [Cited by in F6Publishing: 136]  [Article Influence: 9.1]  [Reference Citation Analysis (0)]
28.  Lecube A, Sampol G, Muñoz X, Lloberes P, Hernández C, Simó R. Insulin resistance is related to impaired lung function in morbidly obese women: a case-control study. Diabetes Metab Res Rev. 2010;26:639-645.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 23]  [Cited by in F6Publishing: 24]  [Article Influence: 1.7]  [Reference Citation Analysis (0)]
29.  Mann JP, Valenti L, Scorletti E, Byrne CD, Nobili V. Nonalcoholic Fatty Liver Disease in Children. Semin Liver Dis. 2018;38:1-13.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 74]  [Cited by in F6Publishing: 84]  [Article Influence: 14.0]  [Reference Citation Analysis (0)]
30.  Forno E, Weiner DJ, Mullen J, Sawicki G, Kurland G, Han YY, Cloutier MM, Canino G, Weiss ST, Litonjua AA. Obesity and Airway Dysanapsis in Children with and without Asthma. Am J Respir Crit Care Med. 2017;195:314-323.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 150]  [Cited by in F6Publishing: 109]  [Article Influence: 15.6]  [Reference Citation Analysis (0)]
31.  Green M, Mead J, Turner JM. Variability of maximum expiratory flow-volume curves. J Appl Physiol. 1974;37:67-74.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 217]  [Cited by in F6Publishing: 222]  [Article Influence: 4.4]  [Reference Citation Analysis (0)]
32.  Mead J. Dysanapsis in normal lungs assessed by the relationship between maximal flow, static recoil, and vital capacity. Am Rev Respir Dis. 1980;121:339-342.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in F6Publishing: 87]  [Reference Citation Analysis (0)]
33.  Suresh S, O’Callaghan M, Sly PD, Mamun AA. Impact of childhood anthropometry trends on adult lung function. Chest. 2015;147:1118-1126.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 27]  [Cited by in F6Publishing: 28]  [Article Influence: 3.1]  [Reference Citation Analysis (0)]
34.  Lazarus R, Colditz G, Berkey CS, Speizer FE. Effects of body fat on ventilatory function in children and adolescents: cross-sectional findings from a random population sample of school children. Pediatr Pulmonol. 1997;24:187-194.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in F6Publishing: 1]  [Reference Citation Analysis (0)]
35.  Pérez-Padilla R, Rojas R, Torres V, Borja-Aburto V, Olaiz G, The Empece Working Group. Obesity among children residing in Mexico City and its impact on lung function: a comparison with Mexican-Americans. Arch Med Res. 2006;37:165-171.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 26]  [Cited by in F6Publishing: 22]  [Article Influence: 1.2]  [Reference Citation Analysis (0)]
36.  Nageswari KS, Sharma R, Kohli DR. Assessment of respiratory and sympathetic cardiovascular parameters in obese school children. Indian J Physiol Pharmacol. 2007;51:235-243.  [PubMed]  [DOI]  [Cited in This Article: ]
37.  Spathopoulos D, Paraskakis E, Trypsianis G, Tsalkidis A, Arvanitidou V, Emporiadou M, Bouros D, Chatzimichael A. The effect of obesity on pulmonary lung function of school aged children in Greece. Pediatr Pulmonol. 2009;44:273-280.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 83]  [Cited by in F6Publishing: 89]  [Article Influence: 5.9]  [Reference Citation Analysis (0)]
38.  Paralikar SJ, Kathrotia RG, Pathak NR, Jani MB. Assessment of pulmonary functions in obese adolescent boys. Lung India. 2012;29:236-240.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 17]  [Cited by in F6Publishing: 18]  [Article Influence: 1.5]  [Reference Citation Analysis (0)]
39.  Khan S, Little J, Chen Y. Relationship Between Adiposity and Pulmonary Function in School-Aged Canadian Children. Pediatr Allergy Immunol Pulmonol. 2014;27:126-132.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 8]  [Cited by in F6Publishing: 8]  [Article Influence: 0.8]  [Reference Citation Analysis (0)]
40.  Torun E, Cakir E, Ozgüç F, Ozgen IT. The effect of obesity degree on childhood pulmonary function tests. Balkan Med J. 2014;31:235-238.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 15]  [Cited by in F6Publishing: 16]  [Article Influence: 1.6]  [Reference Citation Analysis (0)]
41.  Bekkers MB, Wijga AH, Gehring U, Koppelman GH, de Jongste JC, Smit HA, Brunekreef B. BMI, waist circumference at 8 and 12 years of age and FVC and FEV1 at 12 years of age; the PIAMA birth cohort study. BMC Pulm Med. 2015;15:39.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 18]  [Cited by in F6Publishing: 18]  [Article Influence: 2.0]  [Reference Citation Analysis (0)]
42.  Costa Junior D, Peixoto-Souza FS, Araujo PN, Barbalho-Moulin MC, Alves VC, Gomes EL, Costa D. Influence of Body Composition on Lung Function and Respiratory Muscle Strength in Children With Obesity. J Clin Med Res. 2016;8:105-110.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 12]  [Cited by in F6Publishing: 12]  [Article Influence: 1.3]  [Reference Citation Analysis (0)]
43.  Akın O, Arslan M, Haymana C, Karabulut E, Hacihamdioglu B, Yavuz ST. Association of neck circumference and pulmonary function in children. Ann Allergy Asthma Immunol. 2017;119:27-30.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 5]  [Cited by in F6Publishing: 5]  [Article Influence: 0.7]  [Reference Citation Analysis (0)]