Aldosterone Blockade in Chronic Kidney Disease

被引:21
|
作者
Hirsch, Jamie S. [1 ]
Drexler, Yelena [1 ]
Bomback, Andrew S. [1 ]
机构
[1] Columbia Univ Coll Phys & Surg, Dept Med, Div Nephrol, New York, NY 10032 USA
关键词
Aldosterone; chronic kidney disease; proteinuria; spironolactone; CONVERTING ENZYME-INHIBITOR; MINERALOCORTICOID RECEPTOR BLOCKADE; URINARY ALBUMIN EXCRETION; LEFT-VENTRICULAR HYPERTROPHY; STAGE RENAL-DISEASE; ESSENTIAL HYPERTENSIVE PATIENTS; CHRONIC-HEMODIALYSIS PATIENTS; GLOMERULAR-FILTRATION-RATE; CONGESTIVE-HEART-FAILURE; PLACEBO-CONTROLLED TRIAL;
D O I
10.1016/j.semnephrol.2014.04.006
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Although blockade of the renin-angiotensin-aldosterone system with angiotensin-converting enzyme inhibitors or angiotensin-receptor blockers has become standard therapy for chronic kidney disease (CKD), renewed interest in the role of aldosterone in mediating the injuries and progressive insults of CKD has highlighted the potential role of treatments targeting the mineralocorticoid receptor (MR). Although salt restriction is an important component of mitigating the profibrotic effects of MR activation, a growing body of literature has shown that MR antagonists, spironolactone and eplerenone, can reduce proteinuria and blood pressure in patients at all stages of CKD. These agents carry a risk of hyperkalemia, but this risk likely can be predicted based on baseline renal function and mitigated using dietary modifications and adjustments of concomitant medications. Data on hard outcomes, such as progression to end-stage renal disease and overall mortality, still are lacking in patients with CKD. (C) 2014 Elsevier Inc. All rights reserved.
引用
收藏
页码:307 / 322
页数:16
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