个别二肽基肽酶-4 抑制剂与 2 型糖尿病患者的急性肾损伤:系统综述和网络荟萃分析

IF 2.7 4区 医学 Q2 PHARMACOLOGY & PHARMACY
Satoru Mitsuboshi, Makoto Morizumi, Kazumasa Kotake, Ryohei Kaseda, Ichiei Narita
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引用次数: 0

摘要

这项随机对照试验的网络荟萃分析旨在确定是否有任何一种二肽基肽酶-4(DPP-4)抑制剂会增加急性肾损伤(AKI)的风险。我们通过PubMed医学文献分析和检索系统在线版、Cochrane对照试验中央登记册和ClinicalTrials.gov进行了系统检索,以确定相关研究。主要结果为 AKI。采用随机效应模型进行了频数网络荟萃分析,以考虑异质性。共纳入了 29 项研究,涉及 56 117 名参与者。共有 918 例 AKI(1.63%)。一般认为偏倚风险较低。与安慰剂相比,唯一能显著增加 AKI 发生率的 DPP-4 抑制剂是西他列汀(风险比 1.65,95% 置信区间 1.22-2.23)。然而,由于有一项研究在漏斗图中显示出明显的异常值,且研究对象高度异质性,仅包括接受冠状动脉旁路移植手术的患者,因此我们进行了事后敏感性分析,排除了这项研究。结果显示,西他列汀与安慰剂在发生 AKI 的风险上没有统计学意义上的显著差异。单个 DPP-4 抑制剂似乎不会增加 AKI 风险。不过,西他列汀可能会导致有潜在严重心血管疾病的患者发生 AKI。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Individual dipeptidyl peptidase-4 inhibitors and acute kidney injury in patients with type 2 diabetes: A systematic review and network meta-analysis

This network meta-analysis of randomized controlled trials aimed to determine whether any individual dipeptidyl peptidase-4 (DPP-4) inhibitors increase the risk of acute kidney injury (AKI). The Medical Literature Analysis and Retrieval System Online via PubMed, the Cochrane Central Register of Controlled Trials and ClinicalTrials.gov were systematically searched to identify relevant studies. The primary outcome was AKI. A frequentist network meta-analysis was performed using a random-effects model to account for heterogeneity. Twenty-nine studies involving 56 117 participants were included. There were 918 cases of AKI (1.63%). The risk of bias was generally considered to be low. The only DPP-4 inhibitor that significantly increased the frequency of AKI when compared with placebo was sitagliptin (risk ratio 1.65, 95% confidence interval 1.22–2.23). However, because one study showed significant outliers in the funnel plot, in a highly heterogeneous population composed solely of patients undergoing surgery for coronary artery bypass graft, we conducted a post-hoc sensitivity analysis to exclude this study. The results showed no statistically significant difference in the risk of AKI between sitagliptin and placebo. Individual DPP-4 inhibitors do not appear to increase the risk of AKI. However, sitagliptin may be associated with AKI in patients with underlying severe cardiovascular disease.

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来源期刊
CiteScore
5.60
自引率
6.50%
发文量
126
审稿时长
1 months
期刊介绍: Basic & Clinical Pharmacology and Toxicology is an independent journal, publishing original scientific research in all fields of toxicology, basic and clinical pharmacology. This includes experimental animal pharmacology and toxicology and molecular (-genetic), biochemical and cellular pharmacology and toxicology. It also includes all aspects of clinical pharmacology: pharmacokinetics, pharmacodynamics, therapeutic drug monitoring, drug/drug interactions, pharmacogenetics/-genomics, pharmacoepidemiology, pharmacovigilance, pharmacoeconomics, randomized controlled clinical trials and rational pharmacotherapy. For all compounds used in the studies, the chemical constitution and composition should be known, also for natural compounds.
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