Association between SGLT2 (sodium-glucose cotransporter-2) inhibitors and bladder cancer in individuals with type 2 diabetes; a systematic review and meta-analysis
Mobin Mohammadtabar, Alireza Fazeli, Najmeh Parsai, Z. Aboulfathiyarmohammadyar, Erfan Shafiei, Mohamad Khaledi, E. Zaremoghadam, Ali Rahnama Sisakht, Saeid Mohammadi, H. Mardanparvar
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引用次数: 0
Abstract
Introduction: Sodium-glucose cotransporter-2 (SGLT2) inhibitors are the most recent pharmaceutical group for type 2 diabetes (T2D) treatment. Evidence indicates contradictory relationships between sodium-glucose cotransporter-2 inhibitors and bladder cancer (BC). Hence, this study aims to investigate the relationship between SGLT2 inhibitors and BC in patients with T2D. Materials and Methods: This study is a systematic review and meta-analysis based on the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA). International databases including Cochrane, Web of Science, Scopus, PubMed, and Google Scholar were conducted for searching with keywords and without time and language limitations. The reference searching stage continued upgrading until November, 2022. Data analysis was performed with STATA 14 software. The tests with P values lower than 0.05 were considered statistically significant. Results: The four reviewed studies with a sample size comprising 497 755 individuals indicated the impact of SGLT2 inhibitors on BC of patients with T2D (OR: 0.68; 95% CI: 0.37, 1.2). The effect of dapagliflozin, canagliflozin and empagliflozin administration on the incidence of BC among the T2D patients were (OR: 0.72; 95% CI: 0.39, 1.30), (OR: 0.53; 95% CI: 0.23, 1.20), and (OR: 0.51; 95% CI: 0.20, 1.28), respectively. Conclusion: The general conclusion of this study revealed that SGLT2 inhibitors did not increase the risk of BC in T2D patients. The analysis of subgroups also indicated that the administration of dapagliflozin, canagliflozin, and empagliflozin also did not increase the risk of BC in T2D patients. Registration: This study has been compiled based on the PRISMA checklist, and its protocol was registered on the PROSPERO website (ID=CRD42023389014).
引言:钠-葡萄糖协同转运蛋白2(SGLT2)抑制剂是治疗2型糖尿病(T2D)的最新药物组。有证据表明钠-葡萄糖协同转运蛋白-2抑制剂与膀胱癌症(BC)之间存在矛盾关系。因此,本研究旨在探讨SGLT2抑制剂与T2D患者BC之间的关系。材料和方法:本研究是一项基于系统评价和荟萃分析首选报告项目(PRISMA)的系统综述和荟萃分析。包括Cochrane、Web of Science、Scopus、PubMed和Google Scholar在内的国际数据库进行了关键词搜索,没有时间和语言限制。参考搜索阶段继续升级,直到2022年11月。数据分析采用STATA14软件进行。P值低于0.05的测试被认为具有统计学意义。结果:四项回顾性研究的样本量为497755人,表明SGLT2抑制剂对T2D患者BC的影响(OR:0.68;95%CI:0.37,1.2)。达格列嗪、卡格列净和恩帕列嗪给药对T2D病人BC发生率的影响为(OR:0.72;95%CI:0.39,1.30),(OR:0.53;95%CI:0.23,1.20),和(OR:0.51;95%CI:0.20,1.28)。结论:本研究的总体结论表明,SGLT2抑制剂不会增加T2D患者患BC的风险。亚组分析还表明,服用达格列嗪、卡格列净和恩帕列嗪也不会增加T2D患者患BC的风险。注册:本研究基于PRISMA检查表编制,其方案已在PROSPERO网站上注册(ID=CRD42023389014)。