2型糖尿病患者接受钠-葡萄糖共转运体2抑制剂加肾素-血管紧张素系统阻断剂联合疗法的肾脏疗效:基于人群的队列研究

Ming-Hsien Tsai, Ming-chih Chen, Yen-Chun Huang, Wei-Shan Chang, Kai-Yuan Hsiao, Hung-Hsiang Liou, Yu-Wei Fang
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引用次数: 0

摘要

背景:钠-葡萄糖共转运体2抑制剂(SGLT2i)可降低对肾脏的危害,从而使2型糖尿病患者受益。本研究旨在评估钠-葡萄糖共转运体 2 抑制剂(SGLT2i)与传统的肾素-血管紧张素系统阻断剂(RASB)联用,与 RASB 和二肽基肽酶 4 抑制剂(DPP4i)联用相比,是否能对 2 型糖尿病患者的肾脏预后产生协同效应:这是一项回顾性队列研究。研究利用了台湾国民健康保险研究数据库(NHIRD)的数据,包括2016年1月1日至2016年12月31日期间入组的2型糖尿病患者。参与者被分为两组:病例组(n = 3622 人)接受 RASB 加 SGLT2i 治疗,对比组(n = 3622 人)接受 RASB 加 DPP4i 治疗。两组根据性别、年龄和 Charlson 合并症指数进行 1:1 匹配。此外,还使用 TriNetX 进行外部验证:匹配前,未经调整的危险比(HRs)显示,在慢性肾病(CKD)(HR:0.66;95% CI,0.58-0.74)、晚期肾衰竭(HR:0.64;95% CI,0.44-0.93)和开始长期透析(HR:0.61;95% CI,0.38-0.97)方面,SGLT2i 组与对照组存在显著差异。这些差异在配对后仍然显著:CKD(HR:0.74;95% CI,0.65-0.84)、晚期肾衰竭(HR:0.62;95% CI,0.42-0.92)和开始长期透析(HR:0.53;95% CI,0.32-0.87)。在TriNetX数据集中持续观察到了联合疗法对肾脏的益处:局限性:NHIRD缺乏关键的临床因素(如身体特征、实验室数据),回顾性设计可能导致基线差异,尽管TriNexT进行了验证,但其在台湾患者之外的推广性有限:结论:在2型糖尿病患者中,SGLT2i和RASB联合治疗可获得更好的肾脏疗效。
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Renal outcomes of combination therapy with sodium-glucose cotransporter 2 inhibitors plus renin-angiotensin system blockers in patients with type 2 diabetes mellitus: A population-based cohort study
Background: Sodium-glucose cotransporter 2 inhibitors (SGLT2i) can benefit patients with type 2 diabetes mellitus by reducing hazardous renal outcomes. This study aimed to evaluate whether the combination of sodium-glucose cotransporter 2 inhibitors (SGLT2i) and conventional renin-angiotensin system blockers (RASB) provides a synergistic effect on renal outcomes in patients with type 2 diabetes mellitus, compared to the combination of RASB and dipeptidyl peptidase 4 inhibitors (DPP4i). Methods: This is a retrospective cohort study. The study utilized data from the Taiwan National Health Insurance Research Database (NHIRD), including patients with type 2 diabetes mellitus enrolled between January 1, 2016, and December 31, 2016. Participants were divided into two groups: the case group (n = 3,622) receiving RASB plus SGLT2i and the comparison group (n = 3,622) receiving RASB plus DPP4i. The groups were matched 1:1 based on gender, age, and Charlson comorbidity index. Additionally, TriNetX was used for external validation. Results: Prior to matching, unadjusted hazard ratios (HRs) showed significant differences favoring the SGLT2i group for chronic kidney disease (CKD) (HR: 0.66; 95% CI, 0.58–0.74), advanced kidney failure (HR: 0.64; 95% CI, 0.44–0.93), and initiation of long-term dialysis (HR: 0.61; 95% CI, 0.38–0.97). These differences remained significant post-matching: CKD (HR: 0.74; 95% CI, 0.65–0.84), advanced kidney failure (HR: 0.62; 95% CI, 0.42–0.92), and commencement of long-term dialysis (HR: 0.53; 95% CI, 0.32–0.87). The renal benefits of the combination therapy were consistently observed in the TriNetX dataset. Limitations: NHIRD lacks key clinical factors (e.g., physical features, lab data), potential baseline disparities due to retrospective design, and limited generalizability beyond Taiwanese patients, despite TriNexT validation. Conclusions: In patients with type 2 diabetes mellitus, combination therapy with SGLT2i and RASB yielded better renal outcomes.
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