Endothelin A receptor antagonists in diabetic kidney disease

被引:12
作者
Georgianos, Panagiotis I. [1 ]
Agarwal, Rajiv [2 ,3 ]
机构
[1] Aristotle Univ Thessaloniki, AHEPA Hosp, Dept Med 1, Div Nephrol & Hypertens, Thessaloniki, Greece
[2] Indiana Univ Sch Med, Dept Med, Indianapolis, IN 46202 USA
[3] Richard L Roudebush Vet Adm Med Ctr, Indianapolis, IN 46202 USA
关键词
diabetic nephropathy; endothelin antagonism; kidney injury progression; proteinuria; ANGIOTENSIN SYSTEM BLOCKADE; HEART-FAILURE; ATRASENTAN; ALBUMINURIA; NEPHROPATHY; PROTEINURIA; REDUCTION; PROGRESSION; PREDICTORS; AVOSENTAN;
D O I
10.1097/MNH.0000000000000342
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
Purpose of review Despite optimal therapy of diabetic nephropathy with agents blocking the renin-angiotensin-aldosterone system, the residual risk of nephropathy progression to end-stage renal disease (ESRD) remains high. The purpose of this review is to discuss the potential role of endothelin antagonism as a therapeutic tool to reduce residual proteinuria and delay kidney injury progression among patients with diabetic nephropathy. Recent findings Preclinical studies have shown that endothelin receptor antagonists (ERAs) exert proteinuria lowering and nephroprotective actions in experimental models of diabetic nephropathy. ERAs reduce proteinuria in phase 2 trials that included therapy with renin-angiotensin-aldosterone system blockers. Safety of these agents and protection from ESRD needs to be demonstrated in phase 3 trials. Excess risk of fluid retention and heart failure risk remains. Summary The hypothesis that the antiproteinuric effect of endothelin antagonism may be translated into a slower progression of diabetic nephropathy to ESRD is investigated in ongoing randomized trials assessing 'hard' renal endpoints. ERAs may represent a promising tool toward renoprotection in diabetic nephropathy by individualizing therapy and mitigating the risk of heart failure, if these trials are positive.
引用
收藏
页码:338 / 344
页数:7
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