Department of Pharmacoepidemiology, Graduate School of Medicine and Public Health, Kyoto University, Kyoto, Japan.
Department of Diabetes, Endocrinology and Nutrition, Kyoto University Graduate School of Medicine, Kyoto, Japan.
Mayo Clin Proc. 2020 Feb;95(2):265-273. doi: 10.1016/j.mayocp.2019.12.004.
To assess whether sodium-glucose cotransporter-2 inhibitor (SGLT2i) therapy is associated with a favorable renal prognosis for patients with type 2 diabetes melllitus (T2DM) outside the clinical trials setting.
This retrospective study analyzed routinely collected health care records of ∼160 medical institutions in Japan from April 1, 2014, to December 31, 2017/2018 (varying at the institutional level). Adults with T2DM but without end-stage renal disease who initiated either SGLT2i or other classes of glucose-lowering medications (o-GLM) were matched using propensity score. The primary outcome was the time course of estimated glomerular filtration rate (eGFR) displayed in spline curve. The composite of renal worsening (>40% decline in eGFR) and the development of eGFR<30 mL/1.73 m per minute was evaluated as a secondary outcome. Two sensitivity analyses were conducted to determine the robustness of results.
We compared a matched cohort of 1433 SGLT2i users and 2739 o-GLM users (mean age: 61 years). The eGFR declined over time in both groups during the observation period (median: 17 months; maximum: 54 months), with a slower eGFR slope observed in SGLT2i users. This slower decline was consistently observed across different SGLT2i agents and different baseline eGFR groups. The cumulative incidence of composite renal endpoints was lower in the SGLT2i group with a hazard ratio of 0.70 (95% CI, 0.50-0.98; P=.039). Those findings were consistent in sensitivity analyses limited to the period adherent to the initial drug regimen and with a different approach for propensity score calculation.
In a matched cohort of T2DM patients, SGLT2i use was associated with preserved renal function relative to o-GLM use over 2 to 4 years.
评估钠-葡萄糖共转运蛋白 2 抑制剂(SGLT2i)治疗是否与临床试验环境之外的 2 型糖尿病(T2DM)患者的有利肾脏预后相关。
本回顾性研究分析了 2014 年 4 月 1 日至 2017/2018 年 12 月 31 日期间日本约 160 家医疗机构的常规收集的医疗记录(各机构水平不同)。纳入起始使用 SGLT2i 或其他类降糖药物(o-GLM)但无终末期肾病的 T2DM 成人患者,采用倾向评分匹配。主要结局是采用样条曲线显示的估算肾小球滤过率(eGFR)的时间进程。评估肾脏恶化(eGFR 下降>40%)和 eGFR<30 mL/1.73 m 每分的发展的复合终点作为次要结局。进行了两次敏感性分析以确定结果的稳健性。
我们比较了 1433 名 SGLT2i 使用者和 2739 名 o-GLM 使用者的匹配队列(平均年龄:61 岁)。在观察期间,两组的 eGFR 随时间推移而下降(中位数:17 个月;最长:54 个月),SGLT2i 使用者的 eGFR 下降更慢。在不同的 SGLT2i 药物和不同的基线 eGFR 组中均观察到这种较慢的下降。SGLT2i 组的复合肾脏终点累积发生率较低,风险比为 0.70(95%CI,0.50-0.98;P=.039)。在仅限于初始药物治疗期间且采用不同倾向评分计算方法的敏感性分析中,这些发现是一致的。
在 T2DM 患者的匹配队列中,与 o-GLM 相比,SGLT2i 使用在 2 至 4 年内与肾功能保留相关。