Sodium-glucose co-transporter-2 inhibitors and the risk of diabetic ketoacidosis in patients with type 2 diabetes: A systematic review and meta-analysis of randomized controlled trials

被引:127
作者
Liu, Jiali [1 ,2 ]
Li, Ling [1 ,2 ]
Li, Sheyu [3 ]
Wang, Yuning [1 ,2 ]
Qin, Xuan [1 ,2 ]
Deng, Ke [1 ,2 ]
Liu, Yanmei [1 ,2 ]
Zou, Kang [1 ,2 ]
Sun, Xin [1 ,2 ]
机构
[1] Sichuan Univ, West China Hosp, Cochrane China Ctr, Chinese Evidence Based Med Ctr, Chengdu, Peoples R China
[2] Sichuan Univ, West China Hosp, Natl Clin Res Ctr Geriatr, Chengdu, Peoples R China
[3] Sichuan Univ, West China Hosp, Dept Endocrinol & Metab, Chengdu, Peoples R China
基金
中国国家自然科学基金; 中国博士后科学基金;
关键词
SGLT2; inhibitor; type; 2; diabetes; diabetic ketoacidosis; systematic review; meta-analysis; SGLT2; INHIBITORS; CANAGLIFLOZIN; MELLITUS; OUTCOMES; SAFETY;
D O I
10.1111/dom.14075
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Aim To assess the effects of sodium-glucoseco-transporter-2 (SGLT2) inhibitors on diabetic ketoacidosis (DKA) in patients with type 2 diabetes. Materials and Methods We searched PubMed, EMBASE, Cochrane Central Register of Controlled Trials (CENTRAL) and from inception to 13 June 2019 for randomized controlled trials (RCTs) that compared SGLT2 inhibitors with control in patients with type 2 diabetes. Paired reviewers independently screened citations, assessed the risk of bias and extracted data. Peto's method was used as the primary approach to pool the effect of SGLT2 inhibitors on DKA. Sensitivity analyses with the alternative effect measure (risk ratio) or pooling method (Mantel-Haenszel), the use of continuity correction of 0.5 for zero-event trials or a generalized linear mixed model were conducted. Six preplanned subgroup analyses were performed to explore heterogeneity. The grading of recommendations assessment, development and evaluation (GRADE) approach was used to rate the quality of evidence. Results A total of 39 RCTs were included, involving 60 580 patients and 85 DKA events. SGLT2 inhibitors were statistically associated with an increased risk of DKA versus control (SGLT2 inhibitors: 62/34 961 [0.18%] vs. control: 23/25 211 [0.09%], Peto odds ratio [OR] 2.13, 95% confidence interval [CI] 1.38 to 3.27, I-2 = 8%; RD 1.7 more events, 95% CI 0.6 more to 3.4 more events per 1000 over 5 years; high-quality evidence). Sensitivity analyses showed similar results. The subgroup analyses by mean age (interaction P = 0 .02) and length of follow-up (interaction P = 0 .03) showed a larger relative effect among older patients (aged >= 60 years) and those with longer use of SGLT2 inhibitors (>52 weeks). Conclusions High-quality evidence suggests that SGLT2 inhibitors may increase the risk of DKA in patients with type 2 diabetes. The apparent differences in treatment effects among patients of a different age or follow-up were probable, suggesting the advisability of caution in patients with long-term use of SGLT2 inhibitors or in older patients.
引用
收藏
页码:1619 / 1627
页数:9
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