Key result
Semaglutide improves HF symptoms by ~11 points in KCCQ score among the most frail patients.
Why the study?
Frailty is common in HFpEF and semaglutide improves symptoms and reduces body weight in obesity-related HFpEF, but it was unknown whether semaglutide efficacy and safety vary by baseline frailty or whether semaglutide affects frailty burden.
Does semaglutide improve heart failure symptoms and reduce body weight in patients with obesity-related HFpEF across different baseline frailty strata?
RCT (n=1,145)
randomized
Yes
Does semaglutide improve heart failure symptoms and reduce body weight in patients with obesity-related HFpEF across different baseline frailty strata?
Semaglutide improves heart failure symptoms and reduces frailty burden in patients with obesity-related HFpEF, with the greatest symptomatic benefit observed in the most frail patients.
Answers are grounded in this paper and cite their sources.
Captured external expert commentary on this paper, strongest first. Original sources are linked where available.
“GLP-1 receptor agonist (GLP1RA) therapies help patients with obesity‑related heart failure with preserved ejection fraction (HFpEF) feel and function better, but clinicians should monitor for adverse effects, especially in older adults at risk of frailty and sarcopenia.”
Supports semaglutide prioritization in frail obese HFpEF; extends STEP-HFpEF efficacy data across frailty strata.
Frailty is common in heart failure with preserved ejection fraction (HFpEF). In the STEP-HFpEF (Research Study to Investigate How Well Semaglutide Works in People Living With Heart Failure and Obesity) program, semaglutide improved heart failure (HF) symptoms and physical limitations and reduced body weight (BW) in participants with obesity-related HFpEF. Whether the efficacy and safety of semaglutide vary by frailty and the effects of semaglutide on frailty are unknown. This study sought to evaluate the efficacy of semaglutide in participants with obesity-related HFpEF according to frailty status at baseline. The authors performed a prespecified, pooled, participant-level analysis of the STEP-HFpEF program that included participants with obesity-related HFpEF. Participants were randomized to once-weekly semaglutide, 2.4 mg, or placebo for 52 weeks. Dual primary endpoints were changes in Kansas City Cardiomyopathy Questionnaire-Clinical Summary Score (KCCQ-CSS) and BW. Frailty was estimated using a cumulative deficit-derived frailty index comprising 34 variables across multiple domains at baseline and follow-up. Efficacy and safety of semaglutide were evaluated in participants across 3 baseline frailty strata. Effects of semaglutide on frailty burden were also assessed. Of the 1,145 participants, 110 (9.6%) were nonfrail, 343 (30.0%) were more frail, and 692 (60.4%) were most frail. Semaglutide-mediated weight loss was similar across frailty strata (Pinteraction = 0.38). However, the effects of semaglutide on KCCQ-CSS varied by frailty status; participants who were most frail had the greatest improvement at 52 weeks (nonfrail mean difference: -1.5 [95% CI: -8.4 to 5.4]; more frail mean difference: 3.7 [95% CI: -0.2 to 7.6]; most frail mean difference: 11.0 [95% CI: 8.1-13.8]; Pinteraction < 0.001). Semaglutide reduced the burden of frailty during follow-up (OR for being nonfrail at 52 weeks: 3.16 [95% CI: 2.44-4.09]; P < 0.0001). Semaglutide resulted in a similar reduction in BW across frailty subgroups but greater improvements in HF-related symptoms. Moreover, semaglutide reduced frailty burden after 52 weeks of treatment. (Research Study to Investigate How Well Semaglutide Works in People Living With Heart Failure and Obesity [STEP-HFpEF]; NCT04788511) and (Research Study to Look at How Well Semaglutide Works in People Living With Heart Failure, Obesity and Type 2 Diabetes [STEP-HFpEF DM]; NCT04916470).
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Pandey et al. (2025) conducted an RCT in obesity-related HFpEF (n=1,145). Semaglutide vs. Placebo was evaluated on changes in Kansas City Cardiomyopathy Questionnaire-Clinical Summary Score (KCCQ-CSS) and body weight (BW) (MD 11.0, 95% CI 8.1-13.8, p=< 0.001). Semaglutide improved heart failure symptoms most in the most frail participants (MD 11.0; 95% CI 8.1-13.8) and significantly reduced overall frailty burden at 52 weeks (OR 3.16; P<0.0001).
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