Division of Nephrology, Department of Internal Medicine, Mackay Memorial Hospital, Hsinchu, Taiwan; Department of Medicine, MacKay Junior College of Medicine, Nursing and Management, Taipei, Taiwan; Department of Biological Science and Technology, National Chiao Tung University, Hsin-Chu, Taiwan.
Division of Nephrology, Department of Internal Medicine, National Taiwan University Hospital, Taipei, Taiwan.
Mayo Clin Proc. 2018 Dec;93(12):1760-1774. doi: 10.1016/j.mayocp.2018.06.023. Epub 2018 Oct 19.
To focus on the potential beneficial effects of the pleiotropic effects of dipeptidyl peptidase-4 inhibitors (DPP4is) on attenuating progression of diabetic kidney disease in reducing the long-term effect of the acute kidney injury (AKI) to chronic kidney disease (CKD) transition.
Data from the National Health Insurance Research Database from January 1, 1999, to July 31, 2011, were analyzed, and patients with diabetes weaning from dialysis-requiring AKI were identified. Cox proportional hazards models and inverse-weighted estimates of the probability of treatment were used to adjust for treatment selection bias. The outcomes were incident end-stage renal disease (ESRD) and mortality, major adverse cardiovascular events, and hospitalized heart failure.
Of a total of 6165 patients with diabetes weaning from dialysis-requiring AKI identified, 5635 (91.4%) patients were DPP4i nonusers and 530 (8.6%) patients were DPP4i users. Compared with DPP4i nonusers, DPP4i users had a lower risk of ESRD (hazard ratio, 0.81; 95% CI, 0.70-0.94; P=.04) and all-cause mortality (hazard ratio, 0.28; 95% CI, 0.23-0.34; P<.001) after adjustments for CKD, advanced CKD, and angiotensin-converting enzyme inhibitor or angiotensin II receptor blocker use. In contrast, the risk of major adverse cardiovascular events and hospitalized heart failure did not differ significantly between groups.
Dipeptidyl peptidase-4 inhibitor users had a lower risk of ESRD and mortality than did nonusers among patients with diabetes after weaning from dialysis-requiring AKI. Therefore, a prospective study of AKI to CKD transitions after episodes of AKI is needed to optimally target DPP4i interventions.
关注二肽基肽酶-4 抑制剂(DPP4i)的多效作用对减轻糖尿病肾病进展的潜在有益影响,以降低急性肾损伤(AKI)向慢性肾脏病(CKD)转变的长期影响。
分析了 1999 年 1 月 1 日至 2011 年 7 月 31 日期间国家健康保险研究数据库的数据,并确定了正在从需要透析的 AKI 中康复的糖尿病患者。使用 Cox 比例风险模型和治疗概率的逆加权估计来调整治疗选择偏倚。结果是终末期肾病(ESRD)和死亡率、主要不良心血管事件和住院心力衰竭的发生。
在总共 6165 名正在从需要透析的 AKI 中康复的糖尿病患者中,5635 名(91.4%)患者为 DPP4i 非使用者,530 名(8.6%)患者为 DPP4i 使用者。与 DPP4i 非使用者相比,DPP4i 使用者的 ESRD(风险比,0.81;95%CI,0.70-0.94;P=.04)和全因死亡率(风险比,0.28;95%CI,0.23-0.34;P<.001)的风险较低,在调整了 CKD、晚期 CKD 和血管紧张素转换酶抑制剂或血管紧张素 II 受体阻滞剂的使用后。相比之下,两组之间主要不良心血管事件和住院心力衰竭的风险无显著差异。
在从需要透析的 AKI 中康复的糖尿病患者中,与非使用者相比,DPP4i 使用者的 ESRD 和死亡率较低。因此,需要对 AKI 向 CKD 过渡进行前瞻性研究,以优化 DPP4i 干预的目标。