School of Pharmacy, Sungkyunkwan University, Suwon, South Korea.
Research Department of Practice and Policy, School of Pharmacy, University College London, London, UK.
BMJ Open. 2024 Apr 15;14(4):e077084. doi: 10.1136/bmjopen-2023-077084.
To investigate the risk of cardiovascular events associated with commonly used dual and triple therapies of evogliptin, a recently introduced dipeptidyl peptidase-4 inhibitor (DPP4i), for managing type 2 diabetes in routine clinical practice.
A retrospective cohort study.
Korean Health Insurance Review and Assessment database.
Patients who initiated metformin-based dual therapy and metformin+sulfonylurea-based triple therapy in South Korea from 2014 to 2018.
Initiation of combination therapy with evogliptin.
Hazards of cardiovascular events, a composite endpoint of myocardial infarction, heart failure and cerebrovascular events, and its individual components. Cox proportional hazards model with propensity score-based inverse probability of treatment weighting were used to estimate HRs and 95% CIs.
From the dual and triple therapy cohorts, 5830 metformin+evogliptin users and 2198 metformin+sulfonylurea+evogliptin users were identified, respectively. Metformin+evogliptin users, as compared with metformin+non-DPP4i, had a 29% reduced risk of cardiovascular events (HR 0.71, 95% CI 0.62 to 0.82); HRs for individual outcomes were cerebrovascular events (0.71, 95% CI 0.53 to 0.95), heart failure (0.70, 95% CI 0.59 to 0.82), myocardial infarction (0.89, 95% CI 0.60 to 1.31). Metformin+sulfonylurea+evogliptin users, compared with metformin+sulfonylurea+non-DPP4i, had a 24% reduced risk of cardiovascular events (0.76, 95% CI 0.59 to 0.97); HRs for individual outcomes were myocardial infarction (0.57, 95% CI 0.27 to 1.19), heart failure (0.74, 95% CI 0.55 to 1.01), cerebrovascular events (0.96, 95% CI 0.61 to 1.51).
These findings suggest that dual or triple therapies of evogliptin for the management of type 2 diabetes in routine clinical practice present no cardiovascular harms, but could alternatively offer cardiovascular benefits in this patient population.
在常规临床实践中,研究新型二肽基肽酶-4 抑制剂(DPP4i)依格列净联合二甲双胍和二甲双胍+磺酰脲类药物的双重和三重疗法治疗 2 型糖尿病与心血管事件风险的相关性。
回顾性队列研究。
韩国健康保险审查与评估数据库。
2014 年至 2018 年期间在韩国开始二甲双胍为基础的双重疗法和二甲双胍+磺酰脲类药物为基础的三重疗法的患者。
开始联合使用依格列净治疗。
心血管事件(心肌梗死、心力衰竭和脑血管事件的复合终点)及其各个组成部分的风险。采用倾向评分逆概率治疗加权的 Cox 比例风险模型来估计 HRs 和 95%CI。
在双重和三重治疗队列中,分别确定了 5830 名使用二甲双胍+依格列净的患者和 2198 名使用二甲双胍+磺酰脲类药物+依格列净的患者。与使用二甲双胍+非 DPP4i 相比,使用二甲双胍+依格列净的患者心血管事件风险降低了 29%(HR 0.71,95%CI 0.62 至 0.82);各个结局的 HR 为脑血管事件(0.71,95%CI 0.53 至 0.95)、心力衰竭(0.70,95%CI 0.59 至 0.82)和心肌梗死(0.89,95%CI 0.60 至 1.31)。与使用二甲双胍+磺酰脲类药物+非 DPP4i 相比,使用二甲双胍+磺酰脲类药物+依格列净的患者心血管事件风险降低了 24%(0.76,95%CI 0.59 至 0.97);各个结局的 HR 为心肌梗死(0.57,95%CI 0.27 至 1.19)、心力衰竭(0.74,95%CI 0.55 至 1.01)和脑血管事件(0.96,95%CI 0.61 至 1.51)。
这些发现表明,依格列净联合二甲双胍或二甲双胍+磺酰脲类药物治疗 2 型糖尿病在常规临床实践中不会增加心血管风险,反而可能对该患者人群带来心血管获益。