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质子泵抑制剂与新发慢性肾脏病及进展至终末期肾病的风险

Proton Pump Inhibitors and Risk of Incident CKD and Progression to ESRD.

作者信息

Xie Yan, Bowe Benjamin, Li Tingting, Xian Hong, Balasubramanian Sumitra, Al-Aly Ziyad

机构信息

Clinical Epidemiology Center, Veterans Affairs Saint Louis Health Care System.

Department of Medicine, Washington University School of Medicine, Saint Louis, Missouri.

出版信息

J Am Soc Nephrol. 2016 Oct;27(10):3153-3163. doi: 10.1681/ASN.2015121377. Epub 2016 Apr 14.

Abstract

The association between proton pump inhibitors (PPI) use and risk of acute interstitial nephritis has been described. However, whether exposure to PPI associates with incident CKD, CKD progression, or ESRD is not known. We used Department of Veterans Affairs national databases to build a primary cohort of new users of PPI (n=173,321) and new users of histamine H-receptor antagonists (H blockers; n=20,270) and followed these patients over 5 years to ascertain renal outcomes. In adjusted Cox survival models, the PPI group, compared with the H blockers group, had an increased risk of incident eGFR<60 ml/min per 1.73 m and of incident CKD (hazard ratio [HR], 1.22; 95% confidence interval [95% CI], 1.18 to 1.26; and HR, 1.28; 95% CI, 1.23 to 1.34, respectively). Patients treated with PPI also had a significantly elevated risk of doubling of serum creatinine level (HR, 1.53; 95% CI, 1.42 to 1.65), of eGFR decline >30% (HR, 1.32; 95% CI, 1.28 to 1.37), and of ESRD (HR, 1.96; 95% CI, 1.21 to 3.18). Furthermore, we detected a graded association between duration of PPI exposure and risk of renal outcomes among those exposed to PPI for 31-90, 91-180, 181-360, and 361-720 days compared with those exposed for ≤30 days. Examination of risk of renal outcomes in 1:1 propensity score-matched cohorts of patients taking H blockers versus patients taking PPI and patients taking PPI versus controls yielded consistent results. Our results suggest that PPI exposure associates with increased risk of incident CKD, CKD progression, and ESRD.

摘要

质子泵抑制剂(PPI)的使用与急性间质性肾炎风险之间的关联已被描述。然而,PPI暴露是否与新发慢性肾脏病(CKD)、CKD进展或终末期肾病(ESRD)相关尚不清楚。我们利用退伍军人事务部的全国数据库建立了一个主要队列,其中包括PPI新使用者(n = 173321)和组胺H受体拮抗剂(H阻滞剂;n = 20270)新使用者,并对这些患者进行了5年的随访以确定肾脏结局。在调整后的Cox生存模型中,与H阻滞剂组相比,PPI组新发估算肾小球滤过率(eGFR)<60 ml/min/1.73 m²和新发CKD的风险增加(风险比[HR]分别为1.22;95%置信区间[95%CI]为1.18至1.26;以及HR为1.28;95%CI为1.23至1.34)。接受PPI治疗的患者血清肌酐水平翻倍、eGFR下降>30%以及ESRD的风险也显著升高(HR分别为1.53;95%CI为1.42至1.65;HR为1.32;95%CI为1.28至1.37;以及HR为1.96;95%CI为1.21至3.18)。此外,我们发现,与暴露≤30天的患者相比,暴露于PPI 31 - 90天、91 - 180天、181 - 360天和361 - 720天的患者中,PPI暴露持续时间与肾脏结局风险之间存在分级关联。对服用H阻滞剂的患者与服用PPI的患者以及服用PPI的患者与对照组进行1:1倾向评分匹配队列的肾脏结局风险检查,结果一致。我们的结果表明,PPI暴露与新发CKD、CKD进展和ESRD风险增加相关。

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