RELATIONSHIP BETWEEN CIRCULATING LEPTIN AND PERIPHERAL FAT DISTRIBUTION IN OBESE SUBJECTS

Citation
F. Lonnqvist et al., RELATIONSHIP BETWEEN CIRCULATING LEPTIN AND PERIPHERAL FAT DISTRIBUTION IN OBESE SUBJECTS, International journal of obesity, 21(4), 1997, pp. 255-260
Citations number
20
Categorie Soggetti
Nutrition & Dietetics","Endocrynology & Metabolism
ISSN journal
03070565
Volume
21
Issue
4
Year of publication
1997
Pages
255 - 260
Database
ISI
SICI code
0307-0565(1997)21:4<255:RBCLAP>2.0.ZU;2-T
Abstract
BACKGROUND: Abdominal obesity is an important risk factor for the deve lopment of non-insulin dependent diabetes mellitus and other atherogen ic disorders. The recently discovered fat-derived hormone leptin has b een proposed to regulate adiposity through stimulation of satiety and increased energy expenditure. This study was undertaken to examine the relationship between fasting plasma leptin, body fat distribution and atherogenic complications in markedly obese adult subjects. SUBJECTS: The study comprised 29 women and 26 men who all were obese but otherw ise healthy (body mass index, BMI, 33-60 kg/m(2)). RESULTS: In 37 of t he obese subjects, who were characterized in detail, the fasting plasm a leptin levels correlated with plasma insulin (-0.34) but not in a si gnificant way with blood pressure, insulin sensitivity, plasma glucose tolerance or circulating concentrations of glucose, lipoproteins, cat echolamines or plasminogen activator inhibitor-1. In the whole patient material the fasting plasma leptin levels were two times higher in wo men than in men who had similar body mass index values (P < 0.0001), I n spite of the fact that all subjects were massively obese, the plasma leptin values correlated positively with BMI (r=0.39, P=0.004). On th e other hand, there was a negative correlation between plasma leptin a nd waist-to-hip ratio (r=0.65, P=0.0001), which was independent of BMI . CONCLUSION: Except for a quite weak relationship with fasting plasma insulin, leptin appears not to be associated with classical metabolic atherogenic complications to obesity. Instead, it may protect obese s ubjects with a gynoid fat distribution from metabolic complications. A bout 40% of the variation in leptin in massively obese subjects could in fact be explained by peripheral fat distribution.