SAAD AHMED WAQAS MBBS , MUHAMMAD UMER SOHAIL MBBS , MUHAMMAD SAAD MBBS , ABDUL MANNAN KHAN MINHAS MD , STEPHEN J. GREENE MD , MARAT FUDIM MD, MHS , GREGG C. FONAROW MD, MHS , DMITRY ABRAMOV MD , MUHAMMAD SHAHZEB KHAN MD, MSc , RAHEEL AHMED MRCP
{"title":"GLP-1受体激动剂对心力衰竭患者射血分数轻度降低或保留的疗效:系统回顾和荟萃分析","authors":"SAAD AHMED WAQAS MBBS , MUHAMMAD UMER SOHAIL MBBS , MUHAMMAD SAAD MBBS , ABDUL MANNAN KHAN MINHAS MD , STEPHEN J. GREENE MD , MARAT FUDIM MD, MHS , GREGG C. FONAROW MD, MHS , DMITRY ABRAMOV MD , MUHAMMAD SHAHZEB KHAN MD, MSc , RAHEEL AHMED MRCP","doi":"10.1016/j.cardfail.2025.01.022","DOIUrl":null,"url":null,"abstract":"<div><h3>Background</h3><div>Heart failure (HF) with mildly reduced or preserved ejection fraction (HFpEF) accounts for over half of cases of HF, with obesity playing a key role. Residual risk remains high despite available therapies. Glucagon-like peptide-1 receptor agonists (GLP-1RAs) have shown potential cardiometabolic benefits, but their role in HFpEF remains unclear.</div></div><div><h3>Methods</h3><div>A systematic review and meta-analysis of randomized controlled trials evaluating GLP-1RAs in HFpEF were conducted. Studies evaluating GLP-1RA in combination with glucose-dependent insulinotropic polypeptide (GIP) were also included. The analyzed outcomes included cardiovascular (CV) death, worsening HF events and their composite. Hazard ratios (HRs) with 95% confidence intervals (CIs) were pooled by using a random-effects model.</div></div><div><h3>Results</h3><div>Six randomized controlled trials involving 8788 patients were included. GLP-1RAs significantly reduced the composite outcome of CV death or worsening HF events (HR: 0.68 [0.51–0.89]; <em>P</em> = 0.006, I² = 47%) as well as worsening HF events alone (HR: 0.56 [0.38–0.82]; <em>P</em> = 0.003, I² = 51%). No significant reduction was observed for CV death alone (HR: 0.86 [0.67–1.12]; <em>P</em> = 0.27, I² = 0%).</div></div><div><h3>Conclusion</h3><div>GLP-1RAs reduce worsening HF events and the composite of CV death or worsening HF in HFpEF, particularly in patients with obesity or diabetes. These findings support their role as a promising therapy requiring further HFpEF-focused trials.</div></div>","PeriodicalId":15204,"journal":{"name":"Journal of Cardiac Failure","volume":"31 7","pages":"Pages 1076-1080"},"PeriodicalIF":6.7000,"publicationDate":"2025-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Efficacy of GLP-1 Receptor Agonists in Patients With Heart Failure and Mildly Reduced or Preserved Ejection Fraction: A Systematic Review and Meta-Analysis\",\"authors\":\"SAAD AHMED WAQAS MBBS , MUHAMMAD UMER SOHAIL MBBS , MUHAMMAD SAAD MBBS , ABDUL MANNAN KHAN MINHAS MD , STEPHEN J. GREENE MD , MARAT FUDIM MD, MHS , GREGG C. FONAROW MD, MHS , DMITRY ABRAMOV MD , MUHAMMAD SHAHZEB KHAN MD, MSc , RAHEEL AHMED MRCP\",\"doi\":\"10.1016/j.cardfail.2025.01.022\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><h3>Background</h3><div>Heart failure (HF) with mildly reduced or preserved ejection fraction (HFpEF) accounts for over half of cases of HF, with obesity playing a key role. Residual risk remains high despite available therapies. Glucagon-like peptide-1 receptor agonists (GLP-1RAs) have shown potential cardiometabolic benefits, but their role in HFpEF remains unclear.</div></div><div><h3>Methods</h3><div>A systematic review and meta-analysis of randomized controlled trials evaluating GLP-1RAs in HFpEF were conducted. Studies evaluating GLP-1RA in combination with glucose-dependent insulinotropic polypeptide (GIP) were also included. The analyzed outcomes included cardiovascular (CV) death, worsening HF events and their composite. Hazard ratios (HRs) with 95% confidence intervals (CIs) were pooled by using a random-effects model.</div></div><div><h3>Results</h3><div>Six randomized controlled trials involving 8788 patients were included. GLP-1RAs significantly reduced the composite outcome of CV death or worsening HF events (HR: 0.68 [0.51–0.89]; <em>P</em> = 0.006, I² = 47%) as well as worsening HF events alone (HR: 0.56 [0.38–0.82]; <em>P</em> = 0.003, I² = 51%). No significant reduction was observed for CV death alone (HR: 0.86 [0.67–1.12]; <em>P</em> = 0.27, I² = 0%).</div></div><div><h3>Conclusion</h3><div>GLP-1RAs reduce worsening HF events and the composite of CV death or worsening HF in HFpEF, particularly in patients with obesity or diabetes. These findings support their role as a promising therapy requiring further HFpEF-focused trials.</div></div>\",\"PeriodicalId\":15204,\"journal\":{\"name\":\"Journal of Cardiac Failure\",\"volume\":\"31 7\",\"pages\":\"Pages 1076-1080\"},\"PeriodicalIF\":6.7000,\"publicationDate\":\"2025-07-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Cardiac Failure\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S1071916425000910\",\"RegionNum\":2,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"CARDIAC & CARDIOVASCULAR SYSTEMS\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Cardiac Failure","FirstCategoryId":"3","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1071916425000910","RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CARDIAC & CARDIOVASCULAR SYSTEMS","Score":null,"Total":0}
引用次数: 0
摘要
背景:心力衰竭伴轻度射血分数降低或保留(HFpEF)占心力衰竭病例的一半以上,其中肥胖起关键作用。尽管有现有的治疗方法,剩余风险仍然很高。胰高血糖素样肽-1受体激动剂(GLP-1RAs)已显示出潜在的心脏代谢益处,但它们在HFpEF中的作用尚不清楚。方法:对评价HFpEF中GLP-1RAs的随机对照试验(rct)进行系统回顾和荟萃分析。还包括评估GLP-1RA与葡萄糖依赖性胰岛素性多肽(GIP)联合作用的研究。分析的结果包括心血管(CV)死亡、心衰(HF)事件恶化及其复合。风险比(hr)和95%置信区间(ci)采用随机效应模型进行汇总。结果:纳入6项随机对照试验,共8788例患者。GLP-1RAs显著降低CV死亡或心衰恶化事件的综合结局(HR: 0.68 [0.51-0.89], p = 0.006,I² = 47%)以及单独心衰恶化事件的综合结局(HR: 0.56 [0.38-0.82], p = 0.003,I² = 51%)。单独的CV死亡率无显著降低(HR: 0.86 [0.67-1.12], p = 0.27,I² = 0%)。结论:GLP-1RAs可减少HFpEF中恶化的HF事件和CV死亡或恶化HF的复合,特别是在肥胖或糖尿病患者中。这些发现支持了它们作为一种有希望的治疗方法的作用,需要进一步以hfpef为重点的试验。
Efficacy of GLP-1 Receptor Agonists in Patients With Heart Failure and Mildly Reduced or Preserved Ejection Fraction: A Systematic Review and Meta-Analysis
Background
Heart failure (HF) with mildly reduced or preserved ejection fraction (HFpEF) accounts for over half of cases of HF, with obesity playing a key role. Residual risk remains high despite available therapies. Glucagon-like peptide-1 receptor agonists (GLP-1RAs) have shown potential cardiometabolic benefits, but their role in HFpEF remains unclear.
Methods
A systematic review and meta-analysis of randomized controlled trials evaluating GLP-1RAs in HFpEF were conducted. Studies evaluating GLP-1RA in combination with glucose-dependent insulinotropic polypeptide (GIP) were also included. The analyzed outcomes included cardiovascular (CV) death, worsening HF events and their composite. Hazard ratios (HRs) with 95% confidence intervals (CIs) were pooled by using a random-effects model.
Results
Six randomized controlled trials involving 8788 patients were included. GLP-1RAs significantly reduced the composite outcome of CV death or worsening HF events (HR: 0.68 [0.51–0.89]; P = 0.006, I² = 47%) as well as worsening HF events alone (HR: 0.56 [0.38–0.82]; P = 0.003, I² = 51%). No significant reduction was observed for CV death alone (HR: 0.86 [0.67–1.12]; P = 0.27, I² = 0%).
Conclusion
GLP-1RAs reduce worsening HF events and the composite of CV death or worsening HF in HFpEF, particularly in patients with obesity or diabetes. These findings support their role as a promising therapy requiring further HFpEF-focused trials.
期刊介绍:
Journal of Cardiac Failure publishes original, peer-reviewed communications of scientific excellence and review articles on clinical research, basic human studies, animal studies, and bench research with potential clinical applications to heart failure - pathogenesis, etiology, epidemiology, pathophysiological mechanisms, assessment, prevention, and treatment.