Metabolic effects of short-term GLP-1 treatment in insulin resistant heart failure patients

Exp Clin Endocrinol Diabetes. 2012 May;120(5):266-72. doi: 10.1055/s-0032-1304605. Epub 2012 Mar 15.

Abstract

We studied the metabolic effects of 48-h GLP-1 treatment in insulin resistant heart failure patients.In a randomized placebo-controlled double-blinded cross-over study, 11 non-diabetic HF patients with IHD received 48-h GLP-1 and placebo-infusion. We applied OGTT, hyperinsulinemic clamp, indirect calorimetry, forearm, and tracer methods.7 insulin resistant HF (EF 28%±2) patients completed the protocol. GLP-1 decreased plasma glucose levels (p=0.048) and improved glucose tolerance. 4 patients had hypoglycemic events during GLP-1 vs. none during placebo. GLP-1 treatment tended to increase whole body protein turnover (p=0.08) but did not cause muscle wasting. No significant changes in circulating levels of insulin, glucagon, free fatty acids or insulin sensitivity were detected.GLP-1 treatment decreased glucose levels and increased glucose tolerance in insulin resistant HF patients with IHD. Hypoglycemia was common and may limit the use of GLP-1 in these patients. Insulin sensitivity, lipid-, and protein metabolism remained unchanged.Data were collected at the examinational laboratories of Department of Endocrinology and Department of Cardiology, Aarhus University Hospital, Aarhus, Denmark.

Publication types

  • Randomized Controlled Trial
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Blood Glucose / metabolism*
  • Calorimetry, Indirect
  • Cross-Over Studies
  • Double-Blind Method
  • Drug Administration Schedule
  • Fatty Acids, Nonesterified / blood
  • Glucagon / blood
  • Glucagon-Like Peptide 1 / administration & dosage*
  • Glucose Clamp Technique
  • Glucose Tolerance Test
  • Heart Failure / drug therapy*
  • Humans
  • Insulin / blood
  • Insulin Resistance / physiology*
  • Male
  • Middle Aged

Substances

  • Blood Glucose
  • Fatty Acids, Nonesterified
  • Insulin
  • Glucagon-Like Peptide 1
  • Glucagon