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Cardiovascular Effects of Dipeptidyl Peptidase-4 Inhibitors and Glucagon-Like Peptide-1 Receptor Agonists: a Review for the General Cardiologist.

Curr Cardiol Rep · 2020

Last updated 2026-05-28

A review of clinical trials found that DPP-4 inhibitors, a type of diabetes drug, generally do not affect the risk of major heart problems like heart attacks or strokes, but saxagliptin may increase heart failure risk. In contrast, GLP-1 receptor agonists, another diabetes drug class, have been shown to be safe for the heart and some, like liraglutide and semaglutide, reduce the risk of major heart events in people with type 2 diabetes and existing heart disease.

AI summary of the abstract below.

JournalCurr Cardiol Rep, 2020
Citations4
Relative citation ratio0.26
NIH percentile16
Molecules
Conditions studied Type 2 Diabetes, Cardiovascular Risk Reduction

Abstract

PURPOSE OF REVIEW: Results from cardiovascular (CV) outcome trials have revealed important insights into the CV safety and efficacy of glucose-lowering agents, including dipeptidyl peptidase-4 inhibitors (DPP-4i) and glucagon-like peptide-1 receptor agonists (GLP-1RA). RECENT FINDINGS: Among patients with T2DM, DPP-4i have no significant effect on risk of major adverse CV events (MACE: CV death, myocardial infarction, or stroke) with mixed results regarding risk for heart failure (HF). While sitagliptin and linagliptin have neutral effects on HF risk, saxagliptin significantly increases the risk of HF. The CV safety of the GLP-1RA class of medications has been clearly demonstrated, and select agents, such as liraglutide, semaglutide, albiglutide, and dulaglutide, reduce the risk of MACE in patients with T2DM and established CV disease. CV outcome trials have demonstrated CV safety but not incremental efficacy for DPP-4i in most cases. Select GLP-1RA have proven efficacy for MACE and should be considered by cardiologists for CV risk mitigation in the care of patients with T2DM and established CV disease.

Verbatim abstract via PubMed 32770420 ↗