Leptin: a significant indicator of total body fat but not of visceral fat and insulin insensitivity in African-American women

Diabetes. 1996 Nov;45(11):1635-7. doi: 10.2337/diab.45.11.1635.

Abstract

The recently cloned adipose tissue hormone leptin has been proposed to be involved in the neuroendocrine regulation of adiposity and its metabolic sequelae. Visceral fat is known to predict reduced insulin sensitivity and associated adverse metabolic profiles. In this study, we report the first evaluation of the relationships between leptin levels and total body fat, visceral fat, and insulin sensitivity in a cohort of premenopausal African-American women. Thirty-four subjects were analyzed for total fat mass and visceral fat by dual-energy X-ray absorptiometry and computerized axial tomography, respectively. Insulin sensitivity (SI) was assessed using Bergman's minimal model. Results showed that fasting leptin levels strongly correlated with total body fat mass (r = 0.797, P < 0.001). Correlations of leptin with visceral fat (r = 0.54, P < 0.001) and SI (r = -0.419, P = 0.02) were dependent on total body fat. In conclusion, leptin levels reflect total body fat mass, and although visceral fat is known to predict reduced insulin sensitivity independently, leptin did not. Our data thus suggest that diverse mechanisms are responsible for the regulation of total body versus visceral fat distribution, with its metabolic and health risks.

Publication types

  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Adipose Tissue / anatomy & histology*
  • Adipose Tissue / physiology
  • Adult
  • Anthropometry
  • Biomarkers
  • Black or African American
  • Body Constitution
  • Body Mass Index
  • Female
  • Humans
  • Insulin / blood
  • Insulin / metabolism*
  • Insulin / pharmacology
  • Insulin Secretion
  • Leptin
  • Premenopause
  • Proteins / analysis*
  • Recombinant Proteins / pharmacology
  • Regression Analysis
  • White People
  • Wisconsin

Substances

  • Biomarkers
  • Insulin
  • Leptin
  • Proteins
  • Recombinant Proteins