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Comparative outcomes of heart failure among existent classes of anti-diabetic agents: a network meta-analysis of 171,253 participants from 91 randomized controlled trials

机译:现有抗糖尿病药物类别之间心力衰竭的比较结果:来自91项随机对照试验的171,253名参与者的网络荟萃分析

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The cardiovascular (CV) safety in terms of heart failure among different classes of treatment remains largely unknown. We sought to assess the comparative effect of these agents on heart failure outcomes. This study was registered in the International Prospective Register of Systematic Reviews (CRD 42016042063). MEDLINE, EMBASE, and the Cochrane Library Central Register of Controlled Trials were searched. For the primary outcomes reported previously, studies between Jan 1, 1980 and June 30, 2016 were screened, and subsequently updated till Jan 24, 2019. We performed network meta-analysis to obtain estimates for the outcomes of heart failure, in particular by rankograms for ranking of heart failure risk as well as by pairwise comparisons among all classes of anti-diabetic medications. A total of 91 trials were included, among which were 171,253 participants and 4163 reported cases of heart failure events. As for rankograms, the surface under the cumulative ranking curves (SUCRA) of sodium-glucose co-transporters 2 and thiazolidinediones were 93.4% and 4.3%, respectively, signifying the lowest and highest risk of heart failure, respectively. As for pairwise comparisons in the network, sodium-glucose co-transporters 2 were significantly superior to insulin (OR: 0.75, 95% CI 0.62–0.91), dipeptidyl peptidase 4 inhibitors (OR: 0.68, 95% CI 0.59–0.78), glucagon-like peptide-1 receptor agonists (OR: 0.65, 95% CI 0.54–0.78), and thiazolidinediones (OR: 0.46, 95% CI 0.27–0.77) in terms of heart failure risk. Furthermore, in an exploratory analysis among subjects with underlying heart failure or at risk of heart failure, the superiority of sodium-glucose co-transporters 2 was still significant. In terms of heart failure risk, sodium-glucose co-transporters 2 were the most favorable option among all classes of anti-diabetic medications.
机译:在心力衰竭方面,不同治疗类别之间的心血管(CV)安全性仍然未知。我们试图评估这些药物对心力衰竭结果的比较作用。该研究已在国际系统评价预期登记册(CRD 42016042063)中进行了注册。检索MEDLINE,EMBASE和Cochrane图书馆对照试验中央注册簿。对于先前报告的主要结果,筛选了1980年1月1日至2016年6月30日之间的研究,然后更新至2019年1月24日。心力衰竭风险的排名,以及所有类别的抗糖尿病药物之间的成对比较。总共包括91个试验,其中171,253名参与者和4163个报告的心力衰竭事件病例。至于等级图,钠-葡萄糖共转运蛋白2和噻唑烷二酮的累积等级曲线(SUCRA)下的表面分别为93.4%和4.3%,分别表示最低的和最高的心衰风险。至于网络中的成对比较,钠-葡萄糖共转运蛋白2显着优于胰岛素(OR:0.75,95%CI 0.62-0.91),二肽基肽酶4抑制剂(OR:0.68,95%CI 0.59-0.78),就心力衰竭风险而言,胰高血糖素样肽-1受体激动剂(OR:0.65,95%CI 0.54–0.78)和噻唑烷二酮(OR:0.46,95%CI 0.27–0.77)。此外,在具有潜在心力衰竭或有心力衰竭风险的受试者之间的探索性分析中,钠-葡萄糖共转运蛋白2的优越性仍然很明显。就心力衰竭风险而言,钠-葡萄糖共转运蛋白2是所有类型的抗糖尿病药物中最有利的选择。

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