PLASMA LEPTIN LEVELS AND A RESTRICTIVE LUNG IN OBESE THAI CHILDREN AND ADOLESCENTS

Southeast Asian J Trop Med Public Health. 2015 Jan;46(1):116-24.

Abstract

Morbid obesity, the most significant risk factor for development of sev- eral respiratory diseases, is linked to decreased pulmonary function. The aim of this study was to determine the relationships between pulmonary function and plasma levels of homeostasis model assessment-insulin resistance (HOMA-IR), insulin, leptin, hs-CRP and fasting glucose. Values were measured in 39 Thai children and adolescents, divided into three groups according to lung function (forced expiratory volume in one second, FEV1); normal (Group A) FEV1 ≥ 80% (n = 19), obese normal (Group B) FEV1 ≥ 80% (n = 14) and obese (Group C) FEV1 < 80% (n = 6). Body mass index was highest in group C. Groups A and B were comparable for FEV1, forced vital capacity (FVC), maximal voluntary ventilation (MVV) and FEV1/FVC, whereas Group C exhibited significantly reduced FEV1, FVC and MVV but a normal FEV1/FVC ratio. All values except the FEV1/FVC ratio were significantly lower than in groups A and B. Group C had significantly higher levels of leptin, insulin, FG and HOMA-IR than Groups A and B (p < 0.001). There was a significant negative correlation between FEV1 and MVV with leptin, insulin and HOMA-IR, but not with high-sensitivity C-reactive protein (hs-CRP). We conclude that FEV1 is reduced in obese children and adolescents and inversely correlates with plasma leptin, insulin and HOMA-IR levels. We have shown that the most important factor in inducing a restrictive lung in these patients may be related to leptin status.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adolescent
  • Body Mass Index
  • C-Reactive Protein / metabolism
  • Child
  • Female
  • Forced Expiratory Volume / physiology
  • Humans
  • Insulin
  • Insulin Resistance
  • Leptin / blood*
  • Male
  • Pediatric Obesity / physiopathology*
  • Pulmonary Disease, Chronic Obstructive / physiopathology*
  • Risk Factors
  • Vital Capacity / physiology

Substances

  • Insulin
  • Leptin
  • C-Reactive Protein