Impaired incretin response after a mixed meal is associated with insulin resistance in nondiabetic men

Diabetes Care. 2001 Sep;24(9):1640-5. doi: 10.2337/diacare.24.9.1640.

Abstract

Objective: To investigate whether features of the insulin resistance syndrome are associated with altered incretin responses to food intake.

Research design and methods: From a population-based study, 35 men were recruited, representing a wide spectrum of insulin sensitivity and body weight. Each subject underwent a hyperinsulinemic-euglycemic clamp to determine insulin sensitivity. A mixed meal was given, and plasma levels of gastric inhibitory polypeptide (GIP) and glucagon-like peptide 1 (GLP-1), as well as insulin, glucagon, and glucose were measured.

Results: Insulin resistance was associated with impaired GIP and GLP-1 responses to a mixed meal. The total area under the curve (AUC) of the GIP response after the mixed meal was associated with insulin sensitivity (r = 0.54, P < 0.01). There was a significant difference between the highest and the lowest tertile of insulin sensitivity (P < 0.05). GLP-1 levels 15 min after food intake were significantly lower in the most insulin-resistant tertile compared with the most insulin-sensitive tertile. During the first hour, the AUC of GLP-1 correlated significantly with insulin sensitivity (r = 0.47, P < 0.01). Multiple linear regression analysis showed that insulin resistance, but not obesity, was an independent predictor of these decreased incretin responses.

Conclusions: In insulin resistance, the GIP and GLP-1 responses to a mixed meal are impaired and are related to the degree of insulin resistance. Decreased incretin responsiveness may be of importance for the development of impaired glucose tolerance.

Publication types

  • Clinical Trial
  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Biomarkers / blood
  • Blood Glucose / metabolism*
  • Blood Pressure
  • Body Weight
  • Eating*
  • Gastric Inhibitory Polypeptide / blood
  • Gastrointestinal Hormones / blood*
  • Gastrointestinal Hormones / metabolism
  • Glucagon / blood
  • Glucagon-Like Peptide 1
  • Glucagon-Like Peptides
  • Glucose Clamp Technique
  • Humans
  • Insulin / administration & dosage
  • Insulin / blood
  • Insulin / pharmacology
  • Insulin Resistance / physiology*
  • Male
  • Middle Aged
  • Peptide Fragments / blood*
  • Peptide Fragments / metabolism
  • Postprandial Period / physiology*
  • Protein Precursors / blood
  • Regression Analysis

Substances

  • Biomarkers
  • Blood Glucose
  • Gastrointestinal Hormones
  • Insulin
  • Peptide Fragments
  • Protein Precursors
  • glucagon-like peptide 1 (7-36)amide
  • Gastric Inhibitory Polypeptide
  • Glucagon-Like Peptides
  • Glucagon-Like Peptide 1
  • Glucagon