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背景药物对接受 SGLT2 抑制剂的糖尿病患者初始 eGFR 变化及肾脏结局的影响。

The Association of Background Medications on Initial eGFR Change and Kidney Outcomes in Diabetic Patients Receiving SGLT2 Inhibitor.

机构信息

The Cardiovascular Department, Linkou Chang Gung Memorial Hospital, Taoyuan City, Taiwan.

College of Medicine, Chang Gung University, Taoyuan City, Taiwan.

出版信息

Clin J Am Soc Nephrol. 2023 Jul 1;18(7):858-868. doi: 10.2215/CJN.0000000000000159. Epub 2023 Mar 31.

Abstract

BACKGROUND

To determine whether background medications modify the effects of sodium-glucose cotransporter-2 inhibitor (SGLT2i) on the eGFR and kidney outcomes among patients with type 2 diabetes.

METHODS

We used medical data from a multicenter health care facility in Taiwan and included 10,071 patients who received SGLT2i treatment from June 1, 2016, to December 31, 2018. Direct comparisons for use versus no use of specific background drugs were conducted after adjusting for baseline characteristics through propensity score matching. Patients were followed up until the occurrence of composite kidney outcomes (two-fold increase in the serum creatinine level or the development of end-stage kidney disease), mortality, or the end of the study period.

RESULTS

Patients exhibited an initial mean (SEM) decline of -2.72 (0.10) ml/min per 1.73 m 2 in eGFR dip from baseline to a mean treatment duration of 8.1±3.1 weeks after SGLT2i initiation. The eGFR trajectory stabilized 24 weeks after SGLT2i treatment with a mean (SEM) slope of -1.36 (0.25) ml/min per 1.73 m 2 per year. Compared with no drug use, the use of background renin-angiotensin inhibitor ( n =2073), thiazide diuretics ( n =1764), loop diuretics ( n =708), fenofibrate ( n =1043), xanthine oxidase inhibitor ( n =264), and insulin ( n =1656) was associated with a larger initial decrease in eGFR, while background metformin treatment ( n =827) was associated with a smaller initial decrease in eGFR after SGLT2i treatment. The only drugs associated with the long-term composite kidney outcome during SGLT2i treatment were renin-angiotensin inhibitor (hazard ratio [HR], 0.61; 95% confidence interval [CI], 0.40 to 0.95) and loop diuretics (HR, 1.88; 95% CI, 1.19 to 2.96).

CONCLUSIONS

Several background medications were associated with the initial eGFR dip after SGLT2i initiation. Most drugs were not associated with long-term composite kidney outcomes among patients treated with SGLT2i, except for renin-angiotensin system inhibitor associated with favorable outcomes and loop diuretics associated with worse composite kidney outcomes.

摘要

背景

为了确定背景药物是否会改变钠-葡萄糖共转运蛋白 2 抑制剂(SGLT2i)对 2 型糖尿病患者的 eGFR 和肾脏结局的影响。

方法

我们使用了来自台湾一家多中心医疗机构的医疗数据,纳入了 10071 名自 2016 年 6 月 1 日至 2018 年 12 月 31 日接受 SGLT2i 治疗的患者。在通过倾向评分匹配调整基线特征后,对使用与不使用特定背景药物进行了直接比较。对患者进行随访,直至发生复合肾脏结局(血清肌酐水平升高两倍或发展为终末期肾脏疾病)、死亡或研究结束。

结果

患者在开始 SGLT2i 治疗后 8.1±3.1 周内,eGFR 初始平均(SEM)下降-2.72(0.10)ml/min/1.73m 2。在 SGLT2i 治疗 24 周后,eGFR 轨迹稳定,平均(SEM)斜率为每年-1.36(0.25)ml/min/1.73m 2。与未使用药物相比,使用背景肾素-血管紧张素抑制剂(n=2073)、噻嗪类利尿剂(n=1764)、袢利尿剂(n=708)、非诺贝特(n=1043)、黄嘌呤氧化酶抑制剂(n=264)和胰岛素(n=1656)与 eGFR 初始下降更大相关,而背景二甲双胍治疗(n=827)与 SGLT2i 治疗后 eGFR 初始下降较小相关。在 SGLT2i 治疗期间,唯一与长期复合肾脏结局相关的药物是肾素-血管紧张素抑制剂(HR,0.61;95%置信区间[CI],0.40 至 0.95)和袢利尿剂(HR,1.88;95%CI,1.19 至 2.96)。

结论

几种背景药物与 SGLT2i 起始后 eGFR 初始下降有关。除了肾素-血管紧张素系统抑制剂与良好的结局相关和袢利尿剂与较差的复合肾脏结局相关外,大多数药物与接受 SGLT2i 治疗的患者的长期复合肾脏结局无关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6f4e/10356138/db0aeb5c583f/cjasn-18-858-g001.jpg

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