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Effect of GLP-1 Receptor Agonists in Heart Failure with Preserved Ejection Fraction: A Systematic Review and Meta-Analysis.

J Cardiovasc Dev Dis · 2026

Last updated 2026-05-28

A review of six studies involving 5,564 people with heart failure with preserved ejection fraction (HFpEF) found that GLP-1 drugs did not significantly reduce heart-related deaths or worsening heart failure events overall. However, these drugs did improve quality of life and were as safe as placebos, with newer versions like semaglutide and tirzepatide showing a 41% reduction in heart failure events when older drugs like exenatide were excluded.

AI summary of the abstract below.

JournalJ Cardiovasc Dev Dis, 2026
Citations0
Molecules
Conditions studied Heart Failure

Abstract

Heart failure with preserved ejection fraction (HFpEF) affects 32 million people worldwide and is responsible for tens of billions of dollars in healthcare expenditure annually, with costs primarily driven by hospitalizations. HFpEF is notoriously difficult to treat, but emerging studies suggest that glucagon-like peptide-1 receptor agonists (GLP-1 RAs) may be effective therapies. We performed a systematic review and meta-analysis of six randomized controlled trials with 5564 total participants investigating GLP-1 RAs in patients with HFpEF. Overall, no significant effect was noted for GLP-1 RAs on our primary outcomes of cardiovascular mortality and worsening heart failure (HF) events, although they were associated with improvement in quality of life measures. Furthermore, safety data favored the GLP-1 RA group, although tolerability did not differ compared with placebo. While the pooled analysis of all GLP-1 RAs showed neutral effects versus hard endpoints, sensitivity analyses excluding older-generation agents (exenatide) revealed a significant 41% reduction in HF events, suggesting that newer, more potent agents (semaglutide, tirzepatide) may offer disease-modifying benefits in HFpEF. Although future studies are needed, GLP-1 RAs appear to be promising for the treatment of HFpEF.

Verbatim abstract via PubMed 41745350 ↗