Zhang Qi, Zhou Junteng, Wang Yushu, Chen Decai
Department of Endocrinology and Metabolism, West China Hospital of Sichuan UniversityChengdu 610041, Sichuan, China.
Department of Cardiology, West China Hospital of Sichuan UniversityChengdu 610041, Sichuan, China.
Am J Clin Exp Immunol. 2017 Dec 20;6(6):97-106. eCollection 2017.
The Background: Diacerein has been proposed as a treatment option for management of type 2 diabetes due to its anti-inflammatory properties.
The aim of this systematic review and meta-analysis of randomized controlled trials (RCTs) is to examine the effect and safety of diacerein in patients with type 2 diabetes.
We searched Pubmed, Embase, and Cochrane Library for RCTs published from database inception to September 2017.
Among 44 studies that were initially identified, four were eligible and were included in the following analysis. Diacerein significantly reduced fasting glycemia [weighted mean differences (WMD) -0.66, 95% confidence interval (95% CI) -1.16 to -0.16] and glycated hemoglobin A1c (HbA1c ) (WMD -0.85, 95% CI -1.44 to -0.26). And the patients with a diacerein supplementation duration of ≤12 weeks had a greater decrease of fasting glycemia and HbA1c than the supplementation duration of >12 weeks. Furthermore, compared with placebo, diacerein revealed a significant increase in the relative risk (RR) of gastrointestinal symptoms (RR=2.50, 95% CI: 1.10 to 5.65), especially in the study subgroup with supplementation duration of >12 weeks (RR=4.01, 95% CI: 2.32 to 6.95).
The sample size was relatively small and the duration of included studies was short so that the treatment efficacy and safety for longer duration was unknown.
Although further studies are needed, our findings clearly provide support to the use of diacerein in the clinical management of subjects with type 2 diabetes.
背景:由于双醋瑞因具有抗炎特性,已被提议作为2型糖尿病管理的一种治疗选择。
本随机对照试验(RCT)的系统评价和荟萃分析旨在研究双醋瑞因在2型糖尿病患者中的疗效和安全性。
我们在PubMed、Embase和Cochrane图书馆中检索了从数据库建立到2017年9月发表的RCT。
在最初识别的44项研究中,有4项符合条件并纳入以下分析。双醋瑞因显著降低空腹血糖[加权平均差(WMD)-0.66,95%置信区间(95%CI)-1.16至-0.16]和糖化血红蛋白A1c(HbA1c)(WMD -0.85,95%CI -1.44至-0.26)。并且双醋瑞因补充持续时间≤12周的患者空腹血糖和HbA1c的下降幅度大于补充持续时间>12周的患者。此外,与安慰剂相比,双醋瑞因显示胃肠道症状的相对风险(RR)显著增加(RR = 2.50,95%CI:1.10至5.65),尤其是在补充持续时间>12周的研究亚组中(RR = 4.01,95%CI:2.32至6.95)。
样本量相对较小,纳入研究的持续时间较短,因此更长持续时间的治疗疗效和安全性未知。
尽管需要进一步研究,但我们的研究结果明确支持双醋瑞因在2型糖尿病患者临床管理中的应用。