Department of Cardiology, Keio University School of Medicine, Tokyo, Japan.
AstraZeneca K.K., Osaka, Japan.
J Diabetes Investig. 2021 Jan;12(1):67-73. doi: 10.1111/jdi.13321. Epub 2020 Jul 26.
There are limited data on cardiovascular efficacy and safety of type 2 diabetes therapies in Japan, where treatments are characterized by lower metformin use and higher dipeptidyl peptidase-4 inhibitor (DPP4i) use versus other countries. We investigated the cardiovascular outcomes in Japanese patients with type 2 diabetes initiating sodium-glucose cotransporter 2 inhibitors (SGLT2i) matched 1:1 to patients initiating other glucose-lowering drugs (33,890 patients/group) or DPP4i (9,876 patients/group). SGLT2i initiation was associated with lower risks (hazard ratio of in-hospital death [death] 0.56, 95% confidence interval [CI] 0.47-0.67; hospitalization for heart failure 0.75, 95% CI 0.64-0.89; composite of hospitalization for heart failure or death 0.65, 95% CI 0.58-0.74 and stroke 0.66, 95% CI 0.52-0.84 versus other glucose-lowering drugs and lower risks of death 0.52, 95% CI 0.36-0.73) and composite of hospitalization for heart failure or death (0.65, 95% CI 0.51-0.83) versus DPP4i. In conclusion, SGLT2i initiators had lower risks of cardiovascular events versus other glucose-lowering drug initiators and, uniquely, versus DPP4i initiators in Japanese real-world practice.
在日本,心血管疗效和安全性的数据有限,与其他国家相比,日本的治疗方法的特点是使用二甲双胍的比例较低,而使用二肽基肽酶-4 抑制剂(DPP4i)的比例较高。我们调查了起始钠-葡萄糖共转运蛋白 2 抑制剂(SGLT2i)的日本 2 型糖尿病患者的心血管结局,将他们与起始其他降血糖药物(每组 33890 例患者)或 DPP4i(每组 9876 例患者)的患者进行 1:1 匹配。SGLT2i 的起始与较低的风险相关(院内死亡[死亡]的风险比为 0.56,95%置信区间[CI]为 0.47-0.67;心力衰竭住院的风险比为 0.75,95%CI 为 0.64-0.89;心力衰竭或死亡的复合住院风险比为 0.65,95%CI 为 0.58-0.74和中风的风险比为 0.66,95%CI 为 0.52-0.84,与其他降血糖药物相比,SGLT2i 的起始与死亡的风险比为 0.52,95%CI 为 0.36-0.73)和心力衰竭或死亡的复合住院风险比为 0.65,95%CI 为 0.51-0.83,与 DPP4i 相比。总之,在日本的真实世界实践中,SGLT2i 的起始者与其他降血糖药物的起始者相比,具有较低的心血管事件风险,与 DPP4i 的起始者相比,具有独特的较低风险。