Department of Medicine and Therapeutics, Prince of Wales Hospital, The Chinese University of Hong Kong, Shatin, Hong Kong, China.
PLoS One. 2013 May 10;8(5):e62736. doi: 10.1371/journal.pone.0062736. Print 2013.
Laboratory research and previous study suggest that aliskiren, a direct renin inhibitor, has anti-proteinuric effects. We conducted a randomized crossover study to evaluate the anti-proteinuric effect of aliskiren in patients with immunoglobulin A (IgA) nephropathy.
We studied 22 patients with biopsy-proven IgA nephropathy and persistent proteinuria despite angiotensin converting enzyme (ACE) inhibitor or angiotensin receptor blocker (ARB). Patients were randomized to either oral aliskiren 300 mg/day or placebo for 16 weeks and then crossed over to the other treatment arm after a washout period. Proteinuria, estimated glomerular filtration rate (eGFR), blood pressure, and serum potassium were monitored.
After aliskiren treatment, there was a significant reduction in proteinuria in 4 weeks (1.76±0.95 to 1.03±0.69 g:g-Cr, p<0.0001), which remained at a low level throughout the treatment period. There was a significant difference in proteinuria between the aliskiren and placebo groups from 4 to 16 weeks after treatment (p<0.01 for all comparisons). After aliskiren treatment, there were modest but statistically significant reductions in eGFR (57.2±29.1 to 54.8±29.3 ml/min/1.73 m(2), p = 0.013) and diastolic blood pressure (72.6±12.3 to 66.2±11.2 mmHg, p<0.0001). None of the patient developed severe hyperkalemia (serum potassium ≥6.0 mmol/l) during the study period.
Aliskiren has anti-proteinuric effect in patients with IgA nephropathy and persistent proteinuria despite ACE inhibitor or ARB. Further studies are needed to confirm the renal protecting effect of direct renin inhibition in chronic proteinuric kidney diseases.
ClinicalTrials.gov NCT00870493.
实验室研究和先前的研究表明,直接肾素抑制剂阿利西尤单抗具有抗蛋白尿作用。我们进行了一项随机交叉研究,以评估阿利西尤单抗在免疫球蛋白 A (IgA) 肾病患者中的抗蛋白尿作用。
我们研究了 22 例经活检证实的 IgA 肾病患者,这些患者在接受血管紧张素转换酶 (ACE) 抑制剂或血管紧张素受体阻滞剂 (ARB) 治疗后仍有持续性蛋白尿。患者被随机分配接受口服阿利西尤单抗 300mg/天或安慰剂治疗 16 周,然后在洗脱期后交叉至另一治疗组。监测蛋白尿、估计肾小球滤过率 (eGFR)、血压和血清钾。
阿利西尤单抗治疗后,4 周时蛋白尿显著减少(从 1.76±0.95 降至 1.03±0.69 g:g-Cr,p<0.0001),并在整个治疗期间保持在较低水平。治疗后 4 至 16 周时,阿利西尤单抗组与安慰剂组之间的蛋白尿差异有统计学意义(所有比较均 p<0.01)。阿利西尤单抗治疗后,eGFR(从 57.2±29.1 降至 54.8±29.3 ml/min/1.73 m(2),p = 0.013)和舒张压(从 72.6±12.3 降至 66.2±11.2 mmHg,p<0.0001)均有适度但有统计学意义的降低。在研究期间,没有患者发生严重高钾血症(血清钾≥6.0mmol/l)。
阿利西尤单抗可降低 IgA 肾病患者的蛋白尿,即使在接受 ACE 抑制剂或 ARB 治疗后仍有持续性蛋白尿。需要进一步的研究来证实直接肾素抑制在慢性蛋白尿性肾脏疾病中的肾脏保护作用。
ClinicalTrials.gov NCT00870493。