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Effect of add-on direct renin inhibitor aliskiren in patients with non-diabetes related chronic kidney disease

机译:附加的直接肾素抑制剂阿利吉仑对非糖尿病相关慢性肾脏病患者的影响

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Background The renin-angiotensin-aldosterone system (RAAS) plays an important role in the progression of chronic kidney disease (CKD). Although dual RAAS inhibition results in worse renal outcomes than monotherapy in high risk type 2 diabetes patients, the effect of dual RAAS inhibition in patients with non-DM CKD is unclear. The aim of this study was to evaluate the potential renoprotective effect of add-on direct renin inhibitor in non-DM CKD patients. Methods We retrospectively enrolled 189 non-DM CKD patients who had been taking angiotensin II receptor blockers (ARBs) for more than six months. Patients were divided into an add-on aliskiren group and an ARB monotherapy group. The primary outcomes were a decline in glomerular filtration rate (GFR) and a reduction in urinary protein-to-creatinine ratio at six months. Results The baseline characteristics of the two groups were similar. Aliskiren 150 mg daily reduced the urinary protein-to-creatinine ratio by 26% (95% confidence interval, 15 to 37%; p? Conclusion Add-on direct renin inhibitor aliskiren (150 mg daily) safely reduced proteinuria and attenuated the decline in GFR in the non-DM CKD patients who were receiving ARBs.
机译:背景技术肾素-血管紧张素-醛固酮系统(RAAS)在慢性肾脏疾病(CKD)的进展中起重要作用。尽管在高风险的2型糖尿病患者中,双重RAAS抑制导致的肾结局比单药治疗更差,但对非DM CKD患者的双重RAAS抑制作用尚不清楚。这项研究的目的是评估在非DM CKD患者中添加直接肾素抑制剂的潜在肾脏保护作用。方法我们回顾性研究了189例接受血管紧张素II受体阻滞剂(ARB)超过六个月的非DM CKD患者。将患者分为追加阿利吉仑组和ARB单药治疗组。主要结果是六个月时肾小球滤过率(GFR)下降和尿蛋白与肌酐比率降低。结果两组的基线特征相似。每天150 mg Aliskiren可使尿蛋白与肌酐的比例降低26%(95%置信区间为15至37%; p?结论)附加直接肾素抑制剂aliskiren(每天150 mg)可安全降低蛋白尿并减轻尿酸下降。接受ARB的非DM CKD患者的GFR。

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