Effect of ramipril vs amlodipine on renal outcomes in hypertensive nephrosclerosis - A randomized controlled trial

被引:689
作者
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
机构
[1] Louis Stokes, Cleveland VA Med Ctr, Cleveland, OH 44106 USA
[2] NIDDKD, Bethesda, MD 20892 USA
[3] Johns Hopkins Univ, Dept Prevent Med, Baltimore, MD USA
[4] Rush Presbyterian St Lukes Med Ctr, Dept Prevent Med, Chicago, IL 60612 USA
[5] Cleveland Clin Fdn, Dept Biostat, Cleveland, OH 44195 USA
[6] Univ Miami, Dept Med, Coral Gables, FL 33124 USA
[7] Med Univ S Carolina, Dept Med, Charleston, SC 29425 USA
[8] Morehouse Sch Med, Dept Med, Atlanta, GA 30310 USA
[9] Case Western Reserve Univ Hosp, Dept Med, Cleveland, OH 44106 USA
[10] Emory Univ, Med Ctr, Dept Med, Atlanta, GA 30322 USA
[11] Harlem Hosp Med Ctr, Dept Med, New York, NY USA
[12] Meharry Med Coll, Dept Med, Nashville, TN 37208 USA
[13] Mt Sinai Sch Med, Dept Med, New York, NY USA
[14] Ohio State Univ, Dept Med, Columbus, OH 43210 USA
[15] Univ Michigan, Dept Med, Ann Arbor, MI 48109 USA
[16] Univ Calif Los Angeles, Harbor Med Ctr, Dept Med, Los Angeles, CA 90024 USA
[17] Univ Illinois, Dept Med, Chicago, IL USA
[18] Vanderbilt Univ, Dept Med, Nashville, TN USA
[19] Univ So Calif, Dept Med, Los Angeles, CA USA
[20] Univ Texas, SW Med Ctr, Dept Med, Dallas, TX USA
[21] Martin L King Charles R Drew Med Ctr, Dept Med, Los Angeles, CA USA
[22] Univ Calif San Diego, Dept Med, San Diego, CA 92103 USA
[23] Howard Univ, Dept Med, Washington, DC 20059 USA
[24] Univ Alabama Birmingham, Dept Med, Birmingham, AL 35294 USA
[25] Univ Florida, Dept Med, Gainesville, FL USA
来源
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION | 2001年 / 285卷 / 21期
关键词
D O I
10.1001/jama.285.21.2719
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Context incidence of end-stage renal disease due to hypertension has increased in recent decades, but the optimal strategy for treatment of hypertension to prevent renal failure is unknown, especially among African Americans. Objective To compare the effects of an angiotensin-converting enzyme (ACE) inhibitor (ramipril), a dihydropyridine calcium channel blocker (amlodipine), and a beta -blocker (metoprolol) on hypertensive renal disease progression. Design, Setting, and Participants Interim analysis of a randomized, double-blind, 3 x 2 factorial trial conducted in 1094 African Americans aged 18 to 70 years with hypertensive renal disease (glomerular filtration rate [GFR] of 20-65 mL/min per 1.73 m(2)) enrolled between February. 1995 and September 1998. This report compares the ramipril and amlodipine groups following discontinuation of the amlodipine intervention in September 2000. Interventions Participants were randomly assigned to receive amlodipine, 15 to 10 mg/d (n=217), ramipril, 2.5 to 10 mg/d (n=436), or metoprolol, 50 to 200 mg/d (n=441), with other agents added to achieve 1 of 2 blood pressure goals. Main Outcome Measures The primary outcome measure was the rate of change in GFR; the main secondary outcome was a composite index of the clinical end points of reduction in GFR of more than 50% or 25 mL/min per 1.73 m(2), end-stage renal disease, or death. Results Among participants with a urinary protein to creatinine ratio of >0.22 (corresponding approximately to proteinuria of more than 300 mg/d), the ramipril group had a 36% (2.02 [SE, 0.74] mL/min per 1.73 m(2)/y) slower mean decline in GFR over 3 years (P=.006) and a 48% reduced risk of the clinical end points vs the amlodipine group (95% confidence interval [CI], 20%-66%). In the entire cohort, there was no significant difference in mean GFR decline from baseline to 3 years between treatment groups (P=.38). However,compared with the amlodipine group, after adjustment for baseline covariates the ramipril group had a 38% reduced risk of clinical end points (95% CI, 13% -56%), a 36% slower mean decline in GFR after 3 months (P=.002), and less proteinuria (P<.001). Conclusion Ramipril, compared with amlodipine, retards renal disease progression in patients with hypertensive renal disease and proteinuria and may offer benefit to patients without proteinuria.
引用
收藏
页码:2719 / 2728
页数:10
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