Umaña Mejia Carlos Alberto, Sañudo Soto Claudia Victoria, Robalino Juan, Hernández Mayra, Santos Bretón Myriam Bertha, Garcia-Vasquez Edwin A, Rocha Paola, Palacios Brambila Luis Miguel, Morales Sergio, Romo Miguel, Castillo Jaqueline L, Montelongo Quevedo Mauricio, Flores Valdés Jose R
General Medicine, Universidad Autonoma De Guadalajara, Guadalajara, MEX.
General Medicine, Universidad Autónoma De Durango, Sinaloa, MEX.
Cureus. 2025 Jun 2;17(6):e85250. doi: 10.7759/cureus.85250. eCollection 2025 Jun.
Heart failure (HF) is a major global health concern and can be classified into different phenotypes based on left ventricular ejection fraction (LVEF), including heart failure with preserved ejection fraction (HFpEF), reduced ejection fraction, and mildly reduced ejection fraction. This systematic review aims to determine the effect of semaglutide compared to placebo in obese patients with HFpEF. Following PRISMA 2020 guidelines, relevant studies published from January 2021 to August 2024 were identified through searches in PubMed and Science Direct. Randomized clinical trials (RCTs), cohort studies, and case-control studies were considered; however, only two randomized controlled trials (RCTs) and one retrospective cohort ultimately met the inclusion criteria, encompassing a total of 1463 participants with HFpEF and obesity. The risk of bias was evaluated utilizing the Cochrane risk of bias tool for RCTs and the Newcastle-Ottawa Scale (NOS) for the retrospective cohort. In each study, participants were divided into two groups receiving either semaglutide or placebo. The findings after a 52-week follow-up showed that treatment with semaglutide 2.4 mg once weekly resulted in a significant reduction in biomarkers associated with HF. Specifically, baseline C-reactive protein (CRP) values decreased by 43% and 42% in the RCTs and 37% in the retrospective cohort. NT-proBNP levels declined by 20.90% and 23.20% in the RCTs and 15.80% in the cohort, compared to the placebo group. The reductions in CRP and NT-proBNP are clinically relevant, as elevated levels of these biomarkers are associated with worse outcomes in HFpEF. In addition, participants in the semaglutide group experienced a reduction in body weight ranging from 9% to 13% across the three studies, while those in the placebo group showed weight loss between 2% and 7% across the studies. Functional improvement was also observed, with the Kansas City Cardiomyopathy Questionnaire-Clinical Summary Score (KCCQ-CSS) increasing by 13 to 16 points in the semaglutide group compared to the placebo. These results suggest that semaglutide may be a promising treatment for HFpEF in obese patients, offering not only significant weight loss but also improvements in biomarkers and quality of life. Therefore, semaglutide appears to provide potential cardiovascular and metabolic benefits in addition to its established weight-reducing effects, although findings should be interpreted with caution given the limited number of included studies.
心力衰竭(HF)是一个重大的全球健康问题,可根据左心室射血分数(LVEF)分为不同的表型,包括射血分数保留的心力衰竭(HFpEF)、射血分数降低和射血分数轻度降低。本系统评价旨在确定与安慰剂相比,司美格鲁肽对肥胖HFpEF患者的影响。遵循PRISMA 2020指南,通过在PubMed和Science Direct中检索,确定了2021年1月至2024年8月发表的相关研究。纳入了随机临床试验(RCT)、队列研究和病例对照研究;然而,最终只有两项随机对照试验(RCT)和一项回顾性队列研究符合纳入标准,共纳入了1463名HFpEF和肥胖患者。使用Cochrane偏倚风险工具对RCT进行偏倚风险评估,使用纽卡斯尔-渥太华量表(NOS)对回顾性队列进行评估。在每项研究中,参与者被分为两组,分别接受司美格鲁肽或安慰剂。52周随访后的结果表明,每周一次注射2.4 mg司美格鲁肽可显著降低与HF相关的生物标志物。具体而言,在RCT中,基线C反应蛋白(CRP)值下降了43%和42%,在回顾性队列中下降了37%。与安慰剂组相比 在RCT中,NT-proBNP水平下降了20.90%和23.20%,在队列中下降了15.80%。CRP和NT-proBNP的降低具有临床意义,因为这些生物标志物水平升高与HFpEF的不良预后相关。此外,在三项研究中,司美格鲁肽组参与者的体重减轻了9%至13%,而安慰剂组参与者在各项研究中的体重减轻了2%至7%。还观察到功能改善,与安慰剂相比,司美格鲁肽组的堪萨斯城心肌病问卷临床总结评分(KCCQ-CSS)提高了13至16分。这些结果表明,司美格鲁肽可能是肥胖HFpEF患者的一种有前景的治疗方法,不仅能显著减轻体重,还能改善生物标志物和生活质量。因此,尽管纳入研究数量有限,研究结果应谨慎解读,但司美格鲁肽似乎除了已证实的减肥效果外,还能提供潜在的心血管和代谢益处。