Renin-angiotensin system inhibitors in hypertensive adults with non-diabetic CKD with or without proteinuria: a systematic review and meta-analysis of randomized trials

被引:39
作者
Mishima, Eikan [1 ]
Haruna, Yoshisuke [2 ]
Arima, Hisatomi [3 ]
机构
[1] Tohoku Univ, Grad Sch Med, Div Nephrol Endocrinol & Vasc Med, Sendai, Miyagi, Japan
[2] Kawasaki Med Sch, Dept Nephrol & Hypertens, Kurashiki, Okayama, Japan
[3] Fukuoka Univ, Fac Med, Dept Prevent Med & Publ Hlth, Fukuoka, Fukuoka, Japan
关键词
Angiotensin-converting enzyme inhibitors; Angiotensin II receptor blockers; Chronic kidney disease; Proteinuria; !text type='JS']JS[!/text]H 2019 guidelines; CHRONIC KIDNEY-DISEASE; CONVERTING-ENZYME-INHIBITOR; CALCIUM-CHANNEL BLOCKER; CHRONIC-RENAL-FAILURE; II RECEPTOR BLOCKER; BLOOD-PRESSURE; DOUBLE-BLIND; CARDIOVASCULAR EVENTS; ACE-INHIBITION; HEART-FAILURE;
D O I
10.1038/s41440-018-0116-3
中图分类号
R6 [外科学];
学科分类号
1002 ; 100210 ;
摘要
The efficacy and safety of renin-angiotensin system inhibitors (RAS-I) in hypertensive adults with non-diabetic chronic kidney disease (CKD) differ depending on the presence or the absence of proteinuria. To estimate the effects of RAS-I in this population, we performed a systematic review and meta-analysis of randomized controlled trials where treatment with angiotensin-converting-enzyme inhibitors or angiotensin II receptor blockers were compared with placebo or active controls in adults with non-diabetic CKD. The treatment effects were separately reviewed in patients with and without proteinuria. Based on a search of Medline and the Cochrane Library up to September 2017, we identified 42 eligible trials (28, proteinuria-positive group; 6, proteinuria-negative group; 2, mixed-proteinuria group; and 6, proteinuria data-unavailable group). RAS-I reduced renal failure events in comparison to placebo or active agents in the proteinuria-positive group (relative risk [RR] 0.63, 95% confidence interval [CI] 0.52-0.75), but showed no significant effects on renal failure risk in the proteinuria-negative group (RR 0.64, 95% CI 0.18-2.30) although it reduced microalbuminuria. For cardiovascular events, RAS-I was not associated with a significantly reduced risk in both the proteinuria-positive and proteinuria-negative group (RR 0.77 and 1.06, 95% CI 0.51-1.16 and 0.85-1.32, respectively). In the mixed-proteinuria group and proteinuria data-unavailable group, RAS-I showed no significant effects on renal and cardiovascular events. Among adverse events, hyperkalemia increased with RAS-I administration in the proteinuria-positive group (RR 2.01, 95% CI 1.07-3.77). Our analysis showed the renoprotective effects of RAS-I treatment in patients with non-diabetic CKD having proteinuria, supporting its use as the first-line antihypertensive therapy in this population.
引用
收藏
页码:469 / 482
页数:14
相关论文
共 61 条
[1]   Comparison of Clinical Trajectories before Initiation of Renal Replacement Therapy between Diabetic Nephropathy and Nephrosclerosis on the KDIGO Guidelines Heat Map [J].
Abe, Masanori ;
Okada, Kazuyoshi ;
Maruyama, Noriaki ;
Takashima, Hiroyuki ;
Oikawa, Osamu ;
Soma, Masayoshi .
JOURNAL OF DIABETES RESEARCH, 2016, 2016
[2]   Effect of ramipril vs amlodipine on renal outcomes in hypertensive nephrosclerosis - A randomized controlled trial [J].
Agodoa, LY ;
Appel, L ;
Bakris, GL ;
Beck, G ;
Bourgoignie, J ;
Briggs, JP ;
Charleston, J ;
Cheek, D ;
Cleveland, W ;
Douglas, JG ;
Douglas, M ;
Dowie, D ;
Faulkner, M ;
Gabriel, A ;
Gassman, J ;
Greene, T ;
Hall, Y ;
Hebert, L ;
Hiremath, L ;
Jamerson, K ;
Johnson, CJ ;
Kopple, J ;
Kusek, J ;
Lash, J ;
Lea, J ;
Lewis, JB ;
Lipkowitz, M ;
Massry, S ;
Middleton, J ;
Miller, ER ;
Norris, K ;
O'Connor, D ;
Ojo, A ;
Phillips, RA ;
Pogue, V ;
Rahman, M ;
Randall, OS ;
Rostand, S ;
Schulman, G ;
Smith, W ;
Thornley-Brown, D ;
Tisher, CC ;
Toto, RD ;
Wright, JT ;
Xu, SC .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 2001, 285 (21) :2719-2728
[3]   Effects of fosinopril and pravastatin on cardiovascular events in subjects with microalbuminuria [J].
Asselbergs, FW ;
Diercks, GFH ;
Hillege, HL ;
van Boven, AJ ;
Janssen, WMT ;
Voors, AA ;
de Zeeuw, D ;
de Jong, PE ;
van Veldhuisen, DJ ;
van Gilst, WH .
CIRCULATION, 2004, 110 (18) :2809-2816
[4]  
BONNER G, 1993, ARZNEIMITTELFORSCH, V43-2, P852
[5]   Effects of enalapril in systolic heart failure patients with and without chronic kidney disease: Insights from the SOLVD Treatment trial [J].
Bowling, C. Barrett ;
Sanders, Paul W. ;
Allman, Richard M. ;
Rogers, William J. ;
Patel, Kanan ;
Aban, Inmaculada B. ;
Rich, Michael W. ;
Pitt, Bertram ;
White, Michel ;
Bakris, George C. ;
Fonarow, Gregg C. ;
Ahmed, Ali .
INTERNATIONAL JOURNAL OF CARDIOLOGY, 2013, 167 (01) :151-156
[6]   A randomized prospective comparison of nadolol, captopril with or without ticlopidine on disease progression in IgA nephropathy [J].
Cheng, IKP ;
Fang, GX ;
Wong, MC ;
Ji, YL ;
Chan, KW ;
Yeung, HWD .
NEPHROLOGY, 1998, 4 (1-2) :19-26
[7]   Effect of Lisinopril on the progression of renal insufficiency in mild proteinuric non-diabetic nephropathies [J].
Cinotti, GA ;
Zucchelli, PC .
NEPHROLOGY DIALYSIS TRANSPLANTATION, 2001, 16 (05) :961-966
[8]  
Del Vecchio L, 2004, J NEPHROL, V17, P261
[9]   Effect of antihypertensive therapy on renal function and urinary albumin excretion in hypertensive patients with autosomal dominant polycystic kidney disease [J].
Ecder, T ;
Chapman, AB ;
Brosnahan, GM ;
Edelstein, CL ;
Johnson, AM ;
Schrier, RW .
AMERICAN JOURNAL OF KIDNEY DISEASES, 2000, 35 (03) :427-432
[10]   The effects of amlodipine and enalapril on renal function in adults with hypertension and nondiabetic nephropathies: A 3-year, randomized, multicenter, double-blind, placebo-controlled study [J].
Esnault, Vincent L. M. ;
Brown, Edwina A. ;
Apetrei, Eduard ;
Bagon, Jacques ;
Calvo, Carlos ;
DeChatel, Rudolf ;
Holclaas, Hallvard ;
Krcmery, Silvester ;
Kobalava, Zhanna .
CLINICAL THERAPEUTICS, 2008, 30 (03) :482-498