Li Yan-Rong, Wang Chih-Ching, Liu Chi-Hung, Yen Chieh-Li, Wu Victor Chien-Chia, Huang Evelyn Jou-Chen, Lee Ching-Yu, Hsiao Ching-Chung
Division of Endocrinology and Metabolism, Department of Internal Medicine, Linkou Chang Gung Memorial Hospital, Taoyuan, Taiwan.
College of Medicine, Chang Gung University, Taoyuan, Taiwan.
Front Endocrinol (Lausanne). 2024 Aug 30;15:1420485. doi: 10.3389/fendo.2024.1420485. eCollection 2024.
Sodium-glucose co-transporter-2 inhibitors (SGLT2i) have cardiovascular (CV) benefits, particularly in reducing the risk of heart failure (HF). Pioglitazone (Pio) has shown potential in decreasing the risks of recurrent stroke, non-fatal myocardial infarction (MI), and all-cause mortality but increasing risks of HF. Our study aimed to examine the synergistic effects on CV outcomes in patients with type 2 diabetes mellitus (T2DM) who received the combined treatment of SGLT2i and Pio.
A total of 117,850 patients with T2DM and without a history of HF were selected as the observational study cohort from the Chang Gung Research Database (CGRD) in Taiwan between January 1, 2016, and December 31, 2019. The primary composite outcome was 4-point major adverse CV events (4P-MACE), including CV death, non-fatal MI, non-fatal ischemic stroke, and hospitalization for HF. The study was divided into four groups: a combined treatment group in which SGLT2i and Pio were used, two individual groups in which SGLT2i or Pio was used separately, and a reference group (non-study drugs).
Combined treatment of SGLT2i and Pio had the lowest risk of 4P-MACE (adjusted hazard ratio [aHR], 0.66; 95% confidence interval [CI], 0.54-0.80) compared with the reference group after a mean follow-up of 2.2 years. There was no significant difference in risks of hospitalization for HF (adjusted subdistribution hazard ratio, 0.73; 95% CI, 0.49-1.07) compared with the reference group.
In T2DM patients without HF, the combined treatment with SGLT2i and Pio may synergistically provide CV benefits without increasing risks of HF.
钠-葡萄糖协同转运蛋白2抑制剂(SGLT2i)具有心血管(CV)益处,尤其是在降低心力衰竭(HF)风险方面。吡格列酮(Pio)已显示出降低复发性中风、非致命性心肌梗死(MI)和全因死亡率风险的潜力,但会增加HF风险。我们的研究旨在探讨接受SGLT2i和Pio联合治疗的2型糖尿病(T2DM)患者在心血管结局方面的协同作用。
从台湾长庚研究数据库(CGRD)中选取了117850例无HF病史的T2DM患者作为观察性研究队列,时间跨度为2016年1月1日至2019年12月31日。主要复合结局是4点主要不良心血管事件(4P-MACE),包括心血管死亡、非致命性MI、非致命性缺血性中风和HF住院。该研究分为四组:使用SGLT2i和Pio的联合治疗组、分别使用SGLT2i或Pio的两个单药组以及一个参照组(非研究药物组)。
在平均随访2.2年后,与参照组相比,SGLT2i和Pio联合治疗的4P-MACE风险最低(调整后风险比[aHR],0.66;95%置信区间[CI],0.54-0.80)。与参照组相比,HF住院风险无显著差异(调整后亚分布风险比,0.73;95%CI,0.49- 1.07)。
在无HF的T2DM患者中,SGLT2i和Pio联合治疗可能协同提供心血管益处,而不会增加HF风险。