Insulin sensitivity, insulin secretion, and glucose effectiveness in obese subjects: a minimal model analysis

Metabolism. 1995 Nov;44(11):1397-400. doi: 10.1016/0026-0495(95)90136-1.

Abstract

The aim of the present study was to estimate insulin sensitivity (SI), insulin secretion, and glucose effectiveness in 14 obese subjects who were further divided into two groups: one with normal glucose tolerance and the other with impaired glucose tolerance (IGT). Glucose tolerance was determined by criteria of the World Health Organization. All subjects were Japanese. They underwent a modified frequently sampled intravenous glucose tolerance test: glucose (300 mg/kg body weight) was administered, and insulin (20 mU/kg body weight given over 5 minutes) was infused from 20 to 25 minutes after administration of glucose. SI and glucose effectiveness at basal insulin (SG) were estimated by Bergman's minimal model method. Body mass index (33.0 +/- 1.8 v 30.9 +/- 1.5 kg/m2, P > .05) and fasting insulin level (127.9 +/- 30.0 v 107.4 +/- 14.4 pmol/L, P > .05) were higher in obese IGT subjects than in normal obese subjects, but were not statistically significant. With regard to fasting glucose level, obese subjects with IGT (5.9 +/- 0.3 mmol/L) had significantly higher levels than those with normal glucose tolerance (5.1 +/- 0.2 mmol/L, P < .01). There was no significant difference in SI between the two groups (0.53 +/- 0.10 v 0.56 +/- 0.13 x 10(-4).min-1.pmol/L-1, P > .05). Pancreatic insulin secretion expressed as the integrated area of plasma insulin above the basal level during the first 19 minutes was significantly lower in obese subjects with IGT (3,366 +/- 1,495 pmol/L.min) than in those with normal glucose tolerance (16,400 +/- 4,509 pmol/L.min, P < .05).(ABSTRACT TRUNCATED AT 250 WORDS)

MeSH terms

  • Adult
  • Body Mass Index
  • Computer Simulation
  • Female
  • Glucose / metabolism
  • Glucose / pharmacology*
  • Glucose / standards
  • Glucose Tolerance Test
  • Humans
  • Insulin / blood*
  • Insulin / metabolism
  • Insulin Resistance / physiology*
  • Insulin Secretion
  • Islets of Langerhans / cytology
  • Islets of Langerhans / metabolism
  • Islets of Langerhans / physiology
  • Japan / epidemiology
  • Male
  • Middle Aged
  • Models, Biological
  • Obesity / blood*
  • Obesity / epidemiology
  • Obesity / physiopathology*
  • World Health Organization

Substances

  • Insulin
  • Glucose