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Glucagon-like peptide-1 receptor agonists and heart failure in type 2 diabetes: systematic review and meta-analysis of randomized and observational studies

机译:胰高血糖素样肽-1受体激动剂与2型糖尿病心力衰竭:随机和观察性研究的系统评价和荟萃分析

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Background The effect of glucagon-like peptide-1(GLP-1) receptor agonists on heart failure remains uncertain. We therefore conducted a systematic review to assess the possible impact of GLP-1 agonists on heart failure or hospitalization for heart failure in patients with type 2 diabetes. Methods We searched MEDLINE, EMBASE, the Cochrane Central Register of Controlled Trials (CENTRAL) and ClinicalTrials.gov to identify randomized controlled trials (RCTs) and observational studies that addressed the effect of GLP-1 receptor agonists in adults with type 2 diabetes, and explicitly reported heart failure or hospitalization for heart failure. Two paired reviewers screened reports, collected data, and assessed the risk of bias. We pooled data from RCTs and observational studies separately, and used the GRADE approach to rate the quality of evidence. Results We identified 25 studies that were eligible for our review; 21 RCTs ( n =?18,270) and 4 observational studies ( n =?111,029). Low quality evidence from 20 RCTs suggested, if anything, a lower incidence of heart failure between GLP-1 agonists versus control (17/7,441 vs. 19/4,317; odds ratio (OR) 0.62, 95?% confidence interval (CI) 0.31 to 1.22; risk difference (RD) 19 fewer, 95?% CI 34 fewer to 11 more per 1000 over 5?years). Three cohort studies comparing GLP-1 agonists to alternative agents provided very low quality evidence that GLP-1 agonists do not increase the incidence of heart failure. One RCT provided moderate quality evidence that GLP-1 agonists were not associated with hospitalization for heart failure (lixisenatide vs placebo: 122/3,034 vs. 127/3,034; adjusted hazard ratio 0.96, 95?% CI 0.75 to 1.23; RD 4 fewer, 95?% CI 25 fewer to 23 more per 1000 over 5?years) and a case–control study provided very low quality evidence also suggesting no association (GLP-1 agonists vs. other anti-hyperglycemic drugs: 1118 cases and 17,626 controls, adjusted OR 0.67, 95?% CI 0.32 to 1.42). Conclusions The current evidence suggests that GLP-1 agonists do not increase the risk of heart failure or hospitalization for heart failure among patients with type 2 diabetes.
机译:背景胰高血糖素样肽1(GLP-1)受体激动剂对心力衰竭的影响尚不确定。因此,我们进行了系统的评估,以评估GLP-1激动剂对2型糖尿病患者心力衰竭或因心力衰竭住院的可能影响。方法我们搜索了MEDLINE,EMBASE,Cochrane对照试验中心注册中心(CENTRAL)和ClinicalTrials.gov,以鉴定针对2型糖尿病成年人中GLP-1受体激动剂的作用的随机对照试验(RCT)和观察性研究,以及明确报告心力衰竭或因心力衰竭住院。两名成对的审阅者筛选了报告,收集了数据,并评估了偏见的风险。我们分别汇总了来自RCT和观察性研究的数据,并使用GRADE方法对证据质量进行评分。结果我们确定了25项符合我们审查条件的研究。 21个RCT(n = 18,270)和4项观察性研究(n = 111,029)。来自20个RCT的低质量证据表明,如果有的话,GLP-1激动剂与对照组之间心力衰竭的发生率较低(17 / 7,441与19 / 4,317;优势比(OR)0.62,95%置信区间(CI)0.31降低到1.22;风险差异(RD)降低19%,95%CI降低34,而5年内每千分之11更高。三项比较GLP-1激动剂与替代药物的队列研究提供了非常低的质量证据,表明GLP-1激动剂不会增加心力衰竭的发生率。一项RCT提供了中等质量的证据,表明GLP-1激动剂与心力衰竭住院无关(立克塞那肽vs安慰剂:122 / 3,034 vs. 127 / 3,034;调整后的危险比0.96,95%CI 0.75至1.23; RD少4, 95%CI的CI在5年内每1000例中的25例减少到23例以下),并且一项病例对照研究提供的质量非常低的证据也表明没有关联(GLP-1激动剂与其他抗高血糖药物:1118例病例和17,626例对照者,调整后的OR为0.67,95%CI为0.32至1.42)。结论目前的证据表明,GLP-1激动剂不会增加2型糖尿病患者发生心力衰竭或因心力衰竭住院的风险。

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