SGLT2 抑制剂对老年 2 型糖尿病和高血压患者的肾脏保护作用:一项基于真实世界人群的队列研究。

Postgraduate medicine Pub Date : 2024-11-01 Epub Date: 2024-11-13 DOI:10.1080/00325481.2024.2426442
Shasha Geng, Yang Li, Jianli Ge, Yue Liu, Qingqing Li, Xin Chen, Yingqian Zhu, Xiaotong Guo, Huixiao Yuan, Xiaoli Wang, Hua Jiang
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引用次数: 0

摘要

研究目的本研究旨在基于真实世界的临床数据,探讨钠-葡萄糖共转运体 2 抑制剂(SGLT2i)对老年 2 型糖尿病(T2DM)和高血压患者的肾保护作用。该研究旨在为该人群慢性肾病的循证药物治疗提供理论依据:方法:利用上海市卫计委的 "健康云 "平台,对患有 T2DM 和高血压的老年患者进行识别和筛查。进一步构建倾向得分匹配队列,以估计 SGLT2i 对肾功能快速下降(∆eGFR≤-5 ml/min/1.73 m2 或 ∆eGFR%≤-5%)风险的影响。为评估结果的稳健性,进行了多项敏感性分析:结果:经过倾向评分匹配后,SGLT2i 组和非 SGLT2i 组之间的协变量无明显差异。多变量逻辑模型的结果表明,无论是定义为∆eGFR≤-5 ml/min/1.73 m2(OR = 0.60,95% CI:0.38-0.96)还是∆eGFR%≤-5%(OR = 0.57,95% CI:0.37-0.89),使用SGLT2i与eGFR快速下降的风险之间存在一致的反相关性。在肾素-血管紧张素系统抑制剂(RASi)治疗分层中,SGLT2i与RASi组eGFR快速下降风险较低相关(所有ORs p 0.05):结论:SGLT2i 能明显降低 T2DM 和高血压老年患者 eGFR 快速下降的风险,但与 RASi 的协同作用尚不明确。
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Nephroprotective effect of SGLT2 inhibitors in elderly patients with type 2 diabetes mellitus and hypertension: a real-world population-based cohort study.

Objectives: This study aimed to investigate the nephroprotective effect of sodium-glucose cotransporter 2 inhibitors (SGLT2i) in elderly patients with type 2 diabetes mellitus (T2DM) and hypertension based on real-world clinical data. The study aimed to provide a theoretical basis for evidence-based pharmacological treatment of chronic kidney disease in this population.

Methods: The 'Health Cloud' platform of the Shanghai Municipal Health Commission was employed to identify and screen elderly patients with T2DM and hypertension. The propensity score matching cohort was further constructed to estimate the effect of SGLT2i on the risk of rapid decline in renal function (∆eGFR≤-5 mL/min/1.73 m2 or ∆eGFR%≤-5%). Multiple sensitivity analyses were conducted to assess the robustness of the results.

Results: After propensity score matching, no significant differences of covariates were identified between the SGLT2i and non-SGLT2i groups. The results of multivariate logistic models demonstrated a consistent and inverse correlation between SGLT2i use and the risk of rapid eGFR decline, whether defined as ∆eGFR≤-5 mL/min/1.73 m2 (OR = 0.60, 95% CI:0.38-0.96) or ∆eGFR%≤-5% (OR = 0.57, 95% CI:0.37-0.89). In the stratification of renin-angiotensin system inhibitor (RASi) treatment, SGLT2i was associated with a lower risk of rapid eGFR decline in the RASi group (all ORs < 1, p < 0.05), with no interaction between SGLT2i and RASi (all P for interaction > 0.05) detected.

Conclusions: SGLT2i significantly reduced the risk of rapid eGFR decline in elderly patients with T2DM and hypertension, but the synergistic effect with RASi remains unclear.

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