Department of Human Health Sciences, Graduate School of Medicine, Kyoto University, Kyoto 6068507, Japan.
Division of General Internal Medicine and Health Services Research, David Geffen School of Medicine at UCLA, Los Angeles, California 90095, USA.
J Clin Endocrinol Metab. 2022 Dec 17;108(1):221-231. doi: 10.1210/clinem/dgac591.
The preventive effect of sodium-glucose cotransporter 2 (SGLT2) inhibitors for new-onset diabetes was investigated in secondary analyses of several randomized controlled trials (RCTs). However, the results were inconsistent.
This work aimed to synthesize available evidence and evaluate whether SGLT2 inhibitors are effective in preventing new-onset diabetes.
In this systematic review and meta-analysis of RCTs, MEDLINE, EMBASE, and Cochrane Central Register of Controlled Trials were searched through February 11, 2022. Two independent authors screened the search results and extracted summary data from eligible RCTs (including original and post hoc analyses) comparing SGLT2 inhibitors and placebo for the risk of new-onset diabetes among adults with prediabetes. Meta-analysis was conducted using random-effects models to calculate risk ratios and 95% CIs.
We included 4 RCTs with 5655 participants who had prediabetes. Based on the random-effects meta-analysis, SGLT2 inhibitors were significantly associated with a lower risk of new-onset diabetes (relative risk, 0.79; 95% CI, 0.68-0.93). The relative risks of new-onset diabetes in dapagliflozin and empagliflozin were 0.68 (95% CI, 0.52-0.89) and 0.87 (95% CI, 0.72-1.04), respectively (P-for-heterogeneity = .14). The frequency of severe hypoglycemia was not elevated in the SGLT2 inhibitors group compared to the placebo group.
In this meta-analysis, SGLT2 inhibitors were associated with a reduced risk of new-onset type 2 diabetes among adults with prediabetes and heart failure or chronic kidney disease. These findings indicate the potential usefulness of SGLT2 inhibitors in preventing diabetes among high-risk populations with prediabetes.
钠-葡萄糖共转运蛋白 2(SGLT2)抑制剂对新发糖尿病的预防作用已在几项随机对照试验(RCT)的二次分析中进行了研究。然而,结果并不一致。
本研究旨在综合现有证据,评估 SGLT2 抑制剂是否能有效预防新发糖尿病。
在这项对 RCT 的系统评价和荟萃分析中,我们通过 2022 年 2 月 11 日检索了 MEDLINE、EMBASE 和 Cochrane 对照试验中心注册库。两名独立作者筛选检索结果,并从比较 SGLT2 抑制剂与安慰剂在有前驱糖尿病的成年人中新发糖尿病风险的合格 RCT(包括原始和事后分析)中提取汇总数据。使用随机效应模型进行荟萃分析,以计算风险比和 95%置信区间。
我们纳入了 4 项 RCT,共 5655 名有前驱糖尿病的参与者。基于随机效应荟萃分析,SGLT2 抑制剂与新发糖尿病风险降低显著相关(相对风险,0.79;95%置信区间,0.68-0.93)。达格列净和恩格列净的新发糖尿病相对风险分别为 0.68(95%置信区间,0.52-0.89)和 0.87(95%置信区间,0.72-1.04)(P 异质性=0.14)。与安慰剂组相比,SGLT2 抑制剂组严重低血糖的发生频率并未升高。
在这项荟萃分析中,SGLT2 抑制剂与前驱糖尿病合并心力衰竭或慢性肾脏病成年人新发 2 型糖尿病风险降低相关。这些发现表明 SGLT2 抑制剂在预防前驱糖尿病高危人群糖尿病方面具有潜在的作用。