Is there a place for incretin therapies in obesity and prediabetes?

Trends Endocrinol Metab. 2013 Mar;24(3):145-52. doi: 10.1016/j.tem.2013.01.004. Epub 2013 Feb 14.

Abstract

Incretin-based therapies exploit the insulinotropic actions of the gut hormones gastric inhibitory peptide (GIP) and glucagon-like peptide-1 (GLP-1) for the treatment of diabetes and include GLP-1 receptor agonists and inhibitors of dipeptidyl peptidase-4 (DPP-4), the enzyme that inactivates the incretin hormones in the body. Both drug classes improve metabolic control in type 2 diabetes (T2DM), with GLP-1 receptor agonists also lowering body weight. Pharmacotherapy using DPP-4 inhibitors has few side effects and is weight neutral. Animal studies support their use in prediabetes; however, human data are scarce. GLP-1 receptor agonist effects are also apparent in non-diabetic obese individuals. Therefore, incretin-based therapies, if safe, may be effective in preventing progression of prediabetes; and GLP-1 receptor agonists may have potential for use in the treatment of obesity.

Publication types

  • Review

MeSH terms

  • Animals
  • Diabetes Mellitus, Type 2 / drug therapy
  • Dipeptidyl-Peptidase IV Inhibitors / adverse effects
  • Dipeptidyl-Peptidase IV Inhibitors / therapeutic use*
  • Gastric Inhibitory Polypeptide / physiology
  • Gastric Inhibitory Polypeptide / therapeutic use
  • Glucagon-Like Peptide 1 / physiology
  • Glucagon-Like Peptide-1 Receptor
  • Humans
  • Incretins / therapeutic use*
  • Obesity / drug therapy*
  • Obesity / prevention & control
  • Prediabetic State / drug therapy*
  • Prediabetic State / prevention & control
  • Receptors, Glucagon / agonists*

Substances

  • Dipeptidyl-Peptidase IV Inhibitors
  • GLP1R protein, human
  • Glucagon-Like Peptide-1 Receptor
  • Incretins
  • Receptors, Glucagon
  • Gastric Inhibitory Polypeptide
  • Glucagon-Like Peptide 1