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The incretin hormones: from scientific discovery to practical therapeutics.

Diabetologia · 2012

Last updated 2026-05-28

Incretins are gut hormones released after eating that help control blood sugar by boosting insulin release from the pancreas. Two types of incretin-based treatments—GLP-1 agonists and DPP-4 inhibitors—are used for type 2 diabetes and are effective at lowering blood sugar without a high risk of low blood sugar, while also helping with weight management. Research over the past 25 years has shown that people with type 2 diabetes have reduced incretin effects, and treatments like GLP-1 agonists (such as exenatide and liraglutide) and DPP-4 inhibitors (such as sitagliptin and vildagliptin) have been developed to address this.

AI summary of the abstract below.

JournalDiabetologia, 2012
Citations34
Relative citation ratio1.11
NIH percentile54
Molecules
Conditions studied Type 2 Diabetes, Obesity, Cardiovascular Risk Reduction

Abstract

The incretins are gut hormones secreted in response to nutrient/carbohydrate ingestion and act on the pancreatic beta cell to amplify glucose-stimulated insulin secretion. Incretin hormone-based treatments for patients with type 2 diabetes represent a major advance in diabetes therapeutics. The ability of the incretin agents (glucagon-like peptide 1 [GLP-1] agonists and dipeptidyl peptidase IV [DPP-4] inhibitors) to improve glycaemia with a low associated risk of hypoglycaemia, together with beneficial/neutral effects on body weight, offers a significant advantage for both patients and treating clinicians. In this edition of 'Then and Now,' it is useful to look back 25 years and reflect upon the developments in this field since Nauck and colleagues published two seminal papers. In 1986 they first documented a reduced incretin effect in patients with type 2 diabetes (Diabetologia 29:46-52), and then in 1993 they demonstrated that, in patients with poorly controlled type 2 diabetes, a single exogenous infusion of an incretin (GLP-1) increased insulin levels in a glucose-dependent manner and normalised fasting hyperglycaemia (Diabetologia 36:741-744). In the ensuing 26 years, progress in the field of incretin hormones has resulted in a greater understanding of the relative roles of GLP-1 and glucose-dependent insulinotropic polypeptide secretion and activity in the pathogenesis of type 2 diabetes and the important recognition that native GLP-1 is quickly degraded by the ubiquitous protease DPP-4. This has led to the development of GLP-1 agonists that are resistant to degradation by DPP-4 and of selective inhibitors of DPP-4 activity as therapeutic agents. GLP-1 agonists (exenatide and liraglutide) and DPP-4 inhibitors (sitagliptin, vildagliptin, saxagliptin and linagliptin) currently represent effective treatment options for patients with type 2 diabetes. Several additional agents are in the pipeline, including longer acting DPP-4-resistant GLP-1 agonists. More exciting, however, is the increasing recognition that the incretin agents have numerous extra-glycaemic effects that could translate into potential cardiovascular and other benefits.

Verbatim abstract via PubMed 22555471 ↗