Revisiting the association between sodium-glucose cotransporter-2 inhibitors and the risk of neoplasm in patients with type 2 diabetes: new insights from an updated systematic review and meta-analysis of randomized controlled trials

被引:0
|
作者
Wang, Yiran [1 ]
Li, Zonglin [1 ]
Lin, Chu [1 ]
Zhou, Jinyu [1 ]
Cai, Xiaoling [1 ]
Lv, Fang [1 ]
Yang, Wenjia [1 ]
Ji, Linong [1 ]
机构
[1] Peking Univ, Peoples Hosp, Dept Endocrinol & Metab, .11 Xizhimen South St, Beijing 100044, Peoples R China
基金
北京市自然科学基金; 中国国家自然科学基金;
关键词
Sodium-glucose cotransporter-2 inhibitors; neoplasm; type; 2; diabetes; pulmonary neoplasm; prostate neoplasm; SGLT2; INHIBITORS; CANCER; EMPAGLIFLOZIN; MORTALITY; MELLITUS; OUTCOMES;
D O I
暂无
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
ObjectiveTo evaluate the association between sodium-glucose cotransporter-2 inhibitors (SGLT-2i) and the risk of neoplasm in patients with Type 2 diabetes (T2D).MethodsLiterature retrieval was conducted using databases from inception to June 2024. Randomized controlled trials (RCTs) comparing SGLT-2i with placebo or other treatments in patients with T2D, and with reports of neoplasm events were included. Results were computed as the risk ratio (RR) with 95% confidence intervals (CI).ResultsA total of 53 RCTs with 126,232 participants were included. No significant differences were found for the risk of overall neoplasm (RR = 1.08, 95% CI: 0.99 to 1.19, I2 = 23%) in patients with SGLT-2i treatment compared with non-users. However, decreased risk of pulmonary neoplasm (RR = 0.83, 95% CI: 0.69 to 0.99, I2 = 0.0%) was observed in SGLT-2i users compared to non-users, while increased risk of prostate neoplasm in SGLT-2i users was found (RR = 1.21, 95% CI: 1.00 to 1.47, I2 = 0.0%).ConclusionCompared with non-users, the use of SGLT-2i was not associated with the risk of overall neoplasm. However, pulmonary neoplasms were less frequent in SGLT-2i users, while an increased risk of prostate neoplasm was observed in SGLT-2i users compared to non-users.Protocol registrationwww.crd.york.ac.uk/prospero identifier is CRD42021273681.
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页数:9
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