Efficacy and safety of semaglutide in patients with heart failure with preserved ejection fraction and obesity

IF 4.6 Q2 MATERIALS SCIENCE, BIOMATERIALS ACS Applied Bio Materials Pub Date : 2024-05-20 DOI:10.1002/clc.24283
Ayesha Rehman MBBS, Shahab Saidullah MBBS, Muhammad Asad MBBS, Umer R. Gondal MBBS, Amna Ashraf MBBS, Muhammad F. Khan MBBS, Waheed Akhtar MBBS, Amin Mehmoodi MBBS, Jahanzeb Malik MBBS
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Abstract

Background

Semaglutide, a once-weekly glucagon-like peptide-1 receptor agonist, has shown promise in weight management and cardiovascular outcomes in other populations. This study aimed to evaluate the efficacy of semaglutide in heart failure with preserved ejection fraction (HFpEF) patients with obesity.

Methods

A retrospective study analyzed 318 patients with HFpEF, of which 104 received semaglutide and 214 received placebo. Primary endpoints included evaluating changes in exercise capacity and weight management.

Results

Semaglutide treatment led to significant improvements in the primary endpoints. Patients in the semaglutide group demonstrated substantial enhancements in exercise capacity, as measured by the 6-min walk distance, compared to the placebo group (mean difference 15.1 meters, 95% CI 5.8 to 24.4, p = 0.002). Additionally, semaglutide resulted in substantial weight loss compared to placebo (mean difference −2.9%, 95% CI −4.1–−1.7, p = 0.001). Several secondary endpoints, including reductions in C-reactive protein levels and improvements in other clinical parameters, further supported the efficacy of semaglutide. Adverse events were generally well-tolerated, with no unexpected safety concerns.

Conclusion

Semaglutide demonstrated significant clinical benefits in HFpEF patients with obesity, as evidenced by improved symptoms, physical function, and weight reduction.

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塞马鲁肽对射血分数保留型肥胖心力衰竭患者的疗效和安全性。
背景塞马鲁肽是一种每周一次的胰高血糖素样肽-1受体激动剂,已在其他人群中显示出控制体重和改善心血管预后的前景。本研究旨在评估塞马鲁肽对肥胖型射血分数保留型心力衰竭(HFpEF)患者的疗效:一项回顾性研究分析了318名射血分数保留型心力衰竭患者,其中104人接受了semaglutide治疗,214人接受了安慰剂治疗。主要终点包括评估运动能力和体重管理的变化:结果:塞马鲁肽治疗显著改善了主要终点。与安慰剂组相比,以6分钟步行距离为衡量标准,塞马鲁肽组患者的运动能力大幅提高(平均差异为15.1米,95% CI为5.8至24.4,P = 0.002)。此外,与安慰剂组相比,塞马鲁肽还能显著减轻体重(平均差异-2.9%,95% CI -4.1--1.7,p = 0.001)。几个次要终点,包括C反应蛋白水平的降低和其他临床参数的改善,进一步证实了塞马鲁肽的疗效。患者对不良反应的耐受性普遍良好,没有出现意外的安全问题:结论:塞马鲁肽对肥胖型高频血友病患者有显著的临床疗效,表现为症状改善、身体功能改善和体重减轻。
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来源期刊
ACS Applied Bio Materials
ACS Applied Bio Materials Chemistry-Chemistry (all)
CiteScore
9.40
自引率
2.10%
发文量
464
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