Meta-analysis of the association between sodium-glucose co-transporter-2 inhibitors and risk of skin cancer among patients with type 2 diabetes

被引:12
作者
Tang, Huilin [1 ]
Yang, Keming [1 ]
Song, Yiqing [1 ]
Han, Jiali [1 ,2 ]
机构
[1] Indiana Univ, Dept Epidemiol, Richard M Fairbanks Sch Publ Hlth, 1050 Wishard Blvd, Indianapolis, IN 46202 USA
[2] Indiana Univ, Melvin & Bren Simon Canc Ctr, Indianapolis, IN 46204 USA
关键词
beta cell function; clinical physiology; dyslipidaemia; glucose metabolism; insulin resistance; insulin secretion; ADD-ON THERAPY; INADEQUATE GLYCEMIC CONTROL; CHRONIC KIDNEY-DISEASE; DOUBLE-BLIND; EMPAGLIFLOZIN; METFORMIN; 24-WEEK; DAPAGLIFLOZIN; SAFETY; EFFICACY;
D O I
10.1111/dom.13474
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
A slight increase in melanoma risk was observed among sodium-glucose co-transporter-2 (SGLT-2) inhibitor users in the regular reports. However, the association remains uncertain. To address this issue, we performed a systematic search of electronic databases up to May 2, 2018 and a meta-analysis of 21 randomized controlled trials (RCTs) involving 20 308 patients. We did not find a significant increase in risk of melanoma among SGLT-2 inhibitor users (Peto odds ratio [OR], 2.17; 95% confidence interval [CI], 0.80-5.89; I-2, 0%). Similar results were observed in the subgroup analyses according to the type of SGLT-2 inhibitor, type of control, ages of patients, race/ethnicity, and trial durations. For non-melanoma skin cancer risk, no significant difference was observed when all trials were combined (Peto OR, 0.70; 95% CI, 0.47-1.07; I-2, 0%), while a significantly decreased risk was observed among trials with duration <52 weeks (Peto OR, 0.12; 95% CI, 0.02-0.59; I-2, 0%). No evidence of publication bias was detected in the analyses. Current evidence from RCTs did not support a significantly increased risk of skin cancer associated with SGLT-2 inhibitors.
引用
收藏
页码:2919 / 2924
页数:6
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