Department of Endocrinology, Affiliated Hospital of Southwest Medical College, Luzhou, Sichuan 646000, China.
Joslin Diabetes Center, Boston, MA, USA.
Sci Rep. 2017 Mar 9;7:44128. doi: 10.1038/srep44128.
To assess the efficacy and safety of the SGLT-2 inhibitors as adjunct therapy to insulin in T1DM, clinical trials indexed in PubMed, Cochrane Library, EMbase from inception through April 5, 2016. A meta-analysis was conducted on trials of SGLT-2 inhibitors in patients with T1DM on insulin therapy using RevMan 5.3 software. Of the 371 articles identified, ten met eligibility criteria. Seven clinical trials including four randomized controlled trials and 581 patients were included. Compared with the control group, SGLT-2 inhibitors group had significantly reduced fasting plasma glucose by 0.69 mmol/L [1.32; 0.07], glycosylated hemoglobin A1C by 0.37% [0.54; 0.20], body weight by 2.54 kg [3.48; 1.60] and total daily insulin dose by 6.22 IU [8.04; 4.40]. The total incidence of adverse events (AEs), hypoglycemia, and genital and urinary infections were also similar to placebo, while an increased incidence of diabetic ketoacidosis (DKA) (n = 16) was seen in SGLT-2 inhibitors group. The present study demonstrates that SGLT-2 inhibitors are effective as adjunct therapy to insulin in T1DM, heralding improved glycemic control, reduced body weight and total daily insulin dose without an increase in total AEs, hypoglycemia, or genital and urinary infections. However, the risk of DKA should be carefully monitored in future clinical trials.
为了评估 SGLT-2 抑制剂作为胰岛素辅助治疗 T1DM 的疗效和安全性,检索 PubMed、Cochrane Library、EMbase 自建库至 2016 年 4 月 5 日收录的相关临床研究,采用 RevMan 5.3 软件对纳入的 SGLT-2 抑制剂治疗胰岛素治疗的 T1DM 患者的临床研究进行荟萃分析。初检得到 371 篇文献,经筛选符合纳入标准的有 10 篇,共纳入 7 项临床研究,包括 4 项随机对照试验,共 581 例患者。与对照组相比,SGLT-2 抑制剂组空腹血糖降低 0.69mmol/L[1.32;0.07],糖化血红蛋白降低 0.37%[0.54;0.20],体重降低 2.54kg[3.48;1.60],胰岛素日总剂量降低 6.22IU[8.04;4.40]。两组不良反应(AE)、低血糖和泌尿生殖系感染的总发生率相似,而 SGLT-2 抑制剂组糖尿病酮症酸中毒(DKA)的发生率增加(n=16)。本研究表明 SGLT-2 抑制剂作为胰岛素辅助治疗 T1DM 有效,可改善血糖控制,减轻体重和胰岛素日总剂量,不增加 AE、低血糖和泌尿生殖系感染的发生率,但未来临床试验中应密切监测 DKA 的风险。