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除胰岛素治疗外,钠-葡萄糖协同转运蛋白2抑制剂用于2型糖尿病管理:一项随机对照试验的荟萃分析

Sodium-glucose co-transporter 2 inhibitors in addition to insulin therapy for management of type 2 diabetes mellitus: A meta-analysis of randomized controlled trials.

作者信息

Tang Huilin, Cui Wei, Li Dandan, Wang Tiansheng, Zhang Jingjing, Zhai Suodi, Song Yiqing

机构信息

Department of Pharmacy, Peking University Third Hospital, Beijing, China.

Department of Epidemiology, Richard M. Fairbanks School of Public Health, Indiana University, Indianapolis, Indiana.

出版信息

Diabetes Obes Metab. 2017 Jan;19(1):142-147. doi: 10.1111/dom.12785. Epub 2016 Sep 29.

Abstract

Given inconsistent trial results of sodium-glucose cotransporter 2 (SGLT2) inhibitors in addition to insulin therapy for treating type 2 diabetes mellitus (T2DM), a meta-analysis was performed to evaluate the efficacy and safety of this combination for T2DM by searching available randomized trials from PubMed, Embase, CENTRAL and ClinicalTrials.gov. Our meta-analysis included seven eligible placebo-controlled trials involving 4235 patients. Compared with placebo, SGLT2 inhibitor treatment was significantly associated with a mean reduction in HbA1c of -0.56%, fasting plasma glucose of -0.95 mmol/L, body weight of -2.63 kg and insulin dose of -8.79 IU, but an increased risk of drug-related adverse events by 36%, urinary tract infections by 29% and genital infections by 357%. No significant increase was observed in risk of overall adverse events [risk ratio (RR), 1.00], serious adverse events (RR, 0.90), adverse events leading to discontinuation (RR, 1.16), hypoglycaemia events (RR, 1.07) and severe hypoglycaemia events (RR, 1.24). No diabetic ketoacidosis events were reported. Further studies are needed to establish optimal combination type and dose.

摘要

鉴于钠-葡萄糖协同转运蛋白2(SGLT2)抑制剂联合胰岛素治疗2型糖尿病(T2DM)的试验结果不一致,我们通过检索PubMed、Embase、CENTRAL和ClinicalTrials.gov上的随机试验,进行了一项荟萃分析,以评估该联合治疗方案对T2DM的疗效和安全性。我们的荟萃分析纳入了7项符合条件的安慰剂对照试验,涉及4235例患者。与安慰剂相比,SGLT2抑制剂治疗与糖化血红蛋白(HbA1c)平均降低-0.56%、空腹血糖降低-0.95 mmol/L、体重降低-2.63 kg以及胰岛素剂量降低-8.79 IU显著相关,但药物相关不良事件风险增加36%,尿路感染风险增加29%,生殖器感染风险增加357%。总体不良事件风险(风险比[RR],1.00)、严重不良事件(RR,0.90)、导致停药的不良事件(RR,1.16)、低血糖事件(RR,1.07)和严重低血糖事件(RR,1.24)均未观察到显著增加。未报告糖尿病酮症酸中毒事件。需要进一步研究以确定最佳联合类型和剂量。

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