Systematic review and meta-analysis of six RCTs (5,564 participants) evaluating GLP-1 RA effects in HFpEF, incorporating STEP-HFpEF (semaglutide), SUMMIT (tirzepatide), and other trials. Quantifies GLP-1 RA reductions in HF hospitalization, cardiovascular death, KCCQ quality of life, and exercise capacity in HFpEF. Provides pooled evidence that GLP-1 RAs represent an effective new therapeutic class for HFpEF—addressing this historically treatment-refractory form of heart failure that represents over 50% of all HF cases globally.
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.
Authors
Behers, Benjamin J; Sanchez, Christian; Hozayen, Omar; Hozayen, Yousef; Kammer, Rheiner; Corrigan, William T; Stephenson-Moe, Christoph A; Miller, Matthew W; Idriss, Mohab; Cekan, Luis E; King, Alan D; Brown, Garrett H; Hamad, Karen M