Esteghamati Alireza, Noshad Sina, Jarrah Sorour, Mousavizadeh Mostafa, Khoee Seyed Hamid, Nakhjavani Manouchehr
Endocrinology and Metabolism Research Center (EMRC), Vali-Asr Hospital, School of Medicine, Tehran University of Medical Sciences, Tehran, Iran.
Nephrol Dial Transplant. 2013 Nov;28(11):2823-33. doi: 10.1093/ndt/gft281. Epub 2013 Sep 5.
Addition of spironolactone (SPR) to angiotensin-converting enzyme (ACE) inhibitors or angiotensin II receptor blockers (ARBs) might provide antiproteinuric effects beyond what is gained by either medication alone. This study was designed to assess the long-term efficacy of SPR/ARB combination in comparison with the standard ACE/ARB regimen in diabetic nephropathy.
In an open-label, parallel-group, single-center, randomized clinical trial (NCT01667614), 136 patients with diabetes and proteinuria, already treated with enalapril and losartan, were included. In 74 patients, ACE inhibitors were discontinued. After a wash-out period of 2 weeks, 25 mg SPR daily was initiated. The remainder of the patients (n = 62) received ACE inhibitors and ARBs as before. Patients were followed every 3 months for 18 months. During each visit, systolic and diastolic blood pressure (BP), urinary albumin excretion (UAE), serum creatinine, estimated glomerular filtration rate (eGFR) and serum potassium concentrations were determined.
After 18 months, three patients in the SPR/ARB group developed asymptomatic hyperkalemia. SPR/ARB significantly reduced both systolic and diastolic BP (P < 0.001 and 0.001, respectively). SPR/ARB decreased UAE by 46, 72 and 59% after 3, 12 and 18 months, respectively. Compared with the continuation regimen, SPR/ARB was superior in UAE reduction (P = 0.017 after 18 months), independent of BP change. In both groups, eGFR declined significantly over the trial course and the decline rate did not differ significantly between the two groups.
Addition of SPR to ARB provides added benefits with respect to BP control and proteinuria diminution. These antiproteinuric effects are not accompanied by prevention of eGFR loss compared with conventional therapy with ACE/ARB.
在血管紧张素转换酶(ACE)抑制剂或血管紧张素II受体阻滞剂(ARB)基础上加用螺内酯(SPR)可能会产生比单独使用这两种药物更大的抗蛋白尿作用。本研究旨在评估SPR/ARB联合治疗与标准ACE/ARB方案相比在糖尿病肾病中的长期疗效。
在一项开放标签、平行组、单中心随机临床试验(NCT01667614)中,纳入了136例已接受依那普利和氯沙坦治疗的糖尿病蛋白尿患者。74例患者停用ACE抑制剂。经过2周的洗脱期后,开始每日服用25 mg SPR。其余患者(n = 62)继续按之前的方案接受ACE抑制剂和ARB治疗。患者每3个月随访一次,共随访18个月。每次随访时测定收缩压和舒张压(BP)、尿白蛋白排泄率(UAE)、血清肌酐、估算肾小球滤过率(eGFR)和血清钾浓度。
18个月后,SPR/ARB组有3例患者出现无症状性高钾血症。SPR/ARB显著降低了收缩压和舒张压(分别为P < 0.001和0.001)。SPR/ARB在3、12和18个月后分别使UAE降低了46%、72%和59%。与继续治疗方案相比,SPR/ARB在降低UAE方面更具优势(18个月后P = 0.017),且独立于血压变化。在两组中,eGFR在试验过程中均显著下降,两组间下降速率无显著差异。
在ARB基础上加用SPR在控制血压和减少蛋白尿方面具有额外益处。与ACE/ARB传统治疗相比,这些抗蛋白尿作用并未伴随预防eGFR下降。