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PubMed1 Apr 2026·Obesity reviews : an official journal of the International Association for the Study of Obesity● 7/10i

GLP-1 Receptor Agonists for the Prevention of New-Onset Heart Failure: A Systematic Review and Meta-Analysis of Placebo-Controlled Randomized Clinical Trials.

Neves JS, Lobato CB, Leite AR, Vale C, Vasques-Nóvoa F et al.

GLP-1 receptor agonists reduced new-onset heart failure risk by 23% in patients with type 2 diabetes or obesity without existing heart failure. Meta-analysis of 6 placebo-controlled RCTs, 52,752 participants. This establishes primary prevention of heart failure as a new GLP-1 benefit, extending beyond the known secondary prevention data in patients with established HFpEF. The protective effect was independent of glucose or weight control but correlated with cardiovascular benefits.

Strategic signal

FDA will likely require dedicated primary prevention heart failure trials for new GLP-1 label expansions, following the precedent set with SGLT2 inhibitors where Jardiance and Farxiga pursued separate heart failure prevention indications. CMS and commercial payers will face pressure to expand coverage criteria beyond diabetes and obesity to include high cardiovascular risk patients for heart failure prevention, similar to SGLT2 reimbursement evolution. Novo Nordisk and Eli Lilly can leverage this evidence in medical communications to cardiologists, but will need prospective trial data to support formal indication claims.

GLP-1Cardiovascular

Original Abstract

INTRODUCTION: Glucagon-like peptide-1 receptor agonists (GLP-1 RA) improve outcomes in heart failure (HF) with preserved ejection fraction. Whether GLP-1 RA prevent new-onset HF in Type 2 diabetes or obesity requires further investigation. METHODS: We performed an updated meta-analysis of randomized placebo-controlled trials (RCT) of treatment with GLP-1 RA in participants without HF. The hazard ratio (HR) and 95% confidence intervals (95% CI) were extracted from the group without HF in each study. The primary outcome was time to first HF event (HF hospitalization or urgent visit for HF). The correlation between the effect of GLP-1 RA on HF events and the effects on HbA1c, weight and major atherosclerotic cardiovascular events (MACE) was also investigated. We also evaluated the heterogeneity of effect according to study characteristics. RESULTS: A total of 52,752 participants without HF from six RCTs were included. Treatment with GLP-1 RA (vs. placebo) decreased the risk of new-onset HF (HR = 0.77 [95% CI 0.65-0.93], p < 0.001) and the composite of HF events or cardiovascular death (HR = 0.82 [95% CI 0.76-0.89], p < 0.001). The effect of GLP-1 RA on HF events was independent of its effects on HbA1c or weight, but was correlated with its protective effects on MACE. The effects on HF prevention were more pronounced in studies restricted to patients with atherosclerotic cardiovascular disease and in trials with higher incidence rate of HF events. CONCLUSION: Treatment with GLP-1 RA decreases the risk of new-onset HF in patients with Type 2 diabetes or obesity.

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