Department of Medicine, Kidney Center, Tokyo Women's Medical University, Kawada-cho 8-1, Shinjyuku-ku, Tokyo 162-8666, Japan.
Int Urol Nephrol. 2012 Jun;44(3):841-5. doi: 10.1007/s11255-011-9991-0. Epub 2011 May 28.
Blockade of the renin-angiotensin-aldosterone system is a therapeutic mainstay in patients with chronic kidney disease (CKD). However, the renoprotective effect of the novel direct renin inhibitor aliskiren is unknown.
We performed a prospective study in 10 CKD patients. All 10 patients with persistent proteinuria (urinary protein-to-creatinin ratio 0.3-3.5 g/g), despite good blood pressure control (<130/80 mmHg) with olmesartan, were started on 150 mg/day aliskiren. Clinical parameters were examined before and after 4, 8, 12, and 16 weeks of treatment.
Urinary protein-to-creatinine ratio significantly decreased by about 40% at 16 weeks from baseline (P = 0.0002), although estimated glomerular filtration rate and blood pressure did not change throughout the study period. Plasma renin activity also decreased significantly from baseline (P = 0.019), although plasma aldosterone concentration did not change.
Aliskiren combined with olmesartan reduces proteinuria in CKD patients.
血管紧张素转化酶抑制剂阻断剂是慢性肾脏病(CKD)患者的主要治疗方法。然而,新型直接肾素抑制剂阿利克仑的肾保护作用尚不清楚。
我们对 10 名 CKD 患者进行了一项前瞻性研究。所有 10 名持续蛋白尿(尿蛋白/肌酐比值 0.3-3.5 g/g)的患者,尽管用奥美沙坦良好地控制了血压(<130/80 mmHg),都开始服用 150 mg/天的阿利克仑。在治疗前、治疗后 4、8、12 和 16 周时检查临床参数。
与基线相比,16 周时尿蛋白/肌酐比值显著降低约 40%(P=0.0002),尽管整个研究期间估计肾小球滤过率和血压没有变化。血浆肾素活性也从基线显著下降(P=0.019),尽管血浆醛固酮浓度没有变化。
阿利克仑联合奥美沙坦可减少 CKD 患者的蛋白尿。