Key result
GLP-1 RA therapy in diabetic patients with HFrEF was associated with lower risk of HF hospitalization or death at 12 (RR 0.58; 95% CI 0.42-0.77) and 36 months (RR 0.72; 95% CI 0.61-0.85).
Why the study?
This study aimed to evaluate the real-world effectiveness of GLP-1 RAs on clinical outcomes in diabetic patients with heart failure with reduced ejection fraction (HFrEF).
Does glucagon-like peptide-1 receptor agonist therapy reduce the composite of heart failure hospitalization or all-cause mortality in diabetic patients with heart failure with reduced ejection fraction?
Cohort (n=2,618)
Does glucagon-like peptide-1 receptor agonist therapy reduce the composite of heart failure hospitalization or all-cause mortality in diabetic patients with heart failure with reduced ejection fraction?
In a real-world cohort of patients with diabetes and HFrEF, adding a GLP-1 receptor agonist to guideline-directed medical therapy was associated with a significantly lower risk of all-cause mortality or heart failure hospitalization at 1 and 3 years.
Answers are grounded in this paper and cite their sources.
May support GLP-1 RA consideration in diabetic HFrEF; leaves open confirmation in randomized trials.
Aims: To evaluate the effectiveness of GLP-1 RAs on clinical outcomes in diabetic patients with heart failure with reduced ejection fraction (HFrEF). Methods and results: In this retrospective observational cohort study, all adults with diabetes mellitus and HFrEF between 2014 and 2025 were identified. Patients treated with GLP-1 RAs were matched to controls using stratified exact matching. The primary outcome was a composite of heart failure hospitalization or all-cause mortality. Treatment effects were estimated using nonparametric bootstrap resampling (1,000 iterations) to derive risk ratios, NNT estimates, and corresponding 95% confidence intervals. Time-to-event analyses using Cox proportional hazards models were performed as a validation analysis. Among 7,878 patients with HFrEF, 793 (10.1%) patients who initiated GLP-1 RA therapy after HF diagnosis were matched to 1,825 controls. GLP-1 receptor agonist use was associated with a lower risk of heart failure hospitalization or death, with risk ratios of 0.58 (95% CI: 0.42-0.77) at 12 months and 0.72 (95% CI: 0.61-0.85) at 36 months. The combination of high baseline event rates and substantial relative risk reduction translated into remarkably low NNT values in the overall population, with an NNT of 17 (95% CI: 11-33) at 1 year and 13 (95% CI: 8-25) at 3 years. Post hoc subgroup analyses demonstrated consistent effects across clinical subgroups, with no significant heterogeneity observed. Conclusion: In this large real-world cohort of diabetic patients with HFrEF, GLP-1 receptor agonist therapy, in addition to guideline-directed medical therapy, was associated with a lower risk of death or heart failure hospitalization.
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Hammer et al. (2026) conducted a cohort in Diabetes mellitus and heart failure with reduced ejection fraction (HFrEF) (n=2,618). Glucagon-like peptide-1 receptor agonists (GLP-1 RAs) vs. Matched controls not treated with GLP-1 RAs (on guideline-directed medical therapy) was evaluated on Composite of heart failure hospitalization or all-cause mortality (RR 0.72, 95% CI 0.61-0.85). GLP-1 RA therapy in diabetic patients with HFrEF was associated with lower risk of HF hospitalization or death at 12 (RR 0.58; 95% CI 0.42-0.77) and 36 months (RR 0.72; 95% CI 0.61-0.85).
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