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GLP1-GIP receptor co-agonists: a promising evolution in the treatment of type 2 diabetes.

Acta Diabetol · 2024

Last updated 2026-05-28

Tirzepatide is a new type of diabetes and obesity drug that works by activating two gut hormones, GLP-1 and GIP. Clinical trials have tested tirzepatide in people with type 2 diabetes, and it is already approved in several countries for this use.

AI summary of the abstract below.

JournalActa Diabetol, 2024
Citations13
Relative citation ratio2.57
NIH percentile80
Molecules
Conditions studied Type 2 Diabetes

Abstract

Type 2 diabetes represents a growing challenge for global public health. Its prevalence is increasing worldwide, and, like obesity, it affects progressively younger populations compared to the past, with potentially greater impact on chronic complications. Dual glucagon like peptide 1 (GLP1) and glucose-dependent insulinotropic peptide (GIP) receptor agonists are among the new pharmacological strategies recently developed to address this challenge. Tirzepatide, characterized by its ability to selectively bind and activate receptors for the intestinal hormones GIP and GLP-1, has been tested in numerous clinical studies and is already currently authorized in several countries for the treatment of type 2 diabetes and obesity. In this context, the aim of the present document is to summarize, in the form of a narrative literature review, the currently available data on the main mechanisms of action of GIP/GLP-1 co-agonists and the clinical effects of tirzepatide evaluated in various clinical trials.

Verbatim abstract via PubMed 38831203 ↗