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[Cardiovascular effects of GLP-1 receptor agonist treatment: focus on liraglutide].

Vnitr Lek · 2015

Last updated 2026-05-28

Research on GLP-1 drugs like liraglutide suggests they may help reduce cardiovascular risks in people with type 2 diabetes. Studies show these drugs can lower blood pressure, improve blood sugar control, and reduce body weight, though they may slightly increase heart rate. Early data from phase III trials indicate liraglutide has good cardiovascular safety, and further research is ongoing to confirm potential heart-protective effects.

AI summary of the abstract below.

JournalVnitr Lek, 2015
Citations2
Relative citation ratio0.07
NIH percentile6
Molecules liraglutide
Conditions studied Type 2 Diabetes, Cardiovascular Risk Reduction

Abstract

Cardiovascular risk reduction is the major aim of type 2 diabetes mellitus treatment. The effects of various antidiabetics on the cardiovascular complications are currently under careful scrutiny. Incretin-based therapy that utilizes the effects of glucagon-like peptide 1 (GLP-1) or stimulation of its receptor by GLP-1 receptor agonists represents one of the most promising approaches from the potential cardiovascular risk reduction point of view. Experimental studies have shown that the GLP-1 and GLP-1 agonists treatment improves endothelial function, decrease blood pressure and protects myocardium during experimentally-induced ischemia. Clinical studies with GLP-1 receptor agonists consistently show that, in addition to good antidiabetic efficacy, its long-term administration decreases blood pressure, body weight and improves circulating lipid levels while slightly increasing heart rate. In this paper, we focus on the cardiovascular effects of GLP-1 receptor agonist liraglutide. Preliminary analyses of cardiovascular complications in phase III trials with liraglutide indicate its good cardiovascular safety. A possibility of cardioprotective effects of liraglutide remains still open and is currently studied within a prospective cardiovascular trial LEADER.

Verbatim abstract via PubMed 26375689 ↗

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