Intensive Blood-Pressure Control in Hypertensive Chronic Kidney Disease

被引:523
作者
Appel, Lawrence J. [1 ]
Wright, Jackson T., Jr. [2 ]
Greene, Tom [4 ]
Agodoa, Lawrence Y. [5 ]
Astor, Brad C.
Bakris, George L. [6 ]
Cleveland, William H. [8 ]
Charleston, Jeanne
Contreras, Gabriel [10 ]
Faulkner, Marquetta L. [11 ]
Gabbai, Francis B. [13 ,14 ]
Gassman, Jennifer J. [3 ]
Hebert, Lee A. [15 ]
Jamerson, Kenneth A. [16 ]
Kopple, Joel D. [17 ,18 ]
Kusek, John W. [5 ]
Lash, James P. [7 ]
Lea, Janice P. [9 ]
Lewis, Julia B. [12 ]
Lipkowitz, Michael S. [22 ]
Massry, Shaul G. [19 ]
Miller, Edgar R.
Norris, Keith [21 ]
Phillips, Robert A. [25 ]
Pogue, Velvie A. [23 ,24 ]
Randall, Otelio S. [26 ,27 ]
Rostand, Stephen G. [28 ]
Smogorzewski, Miroslaw J. [20 ]
Toto, Robert D. [29 ]
Wang, Xuelei [3 ]
机构
[1] Johns Hopkins Univ, Johns Hopkins Med Inst, Welch Ctr Prevent Epidemiol & Clin Res, Baltimore, MD 21205 USA
[2] Case Western Reserve Univ, Dept Med, Cleveland, OH 44106 USA
[3] Cleveland Clin Fdn, Dept Quantitat Hlth Sci, Cleveland, OH 44195 USA
[4] Univ Utah, Sch Med, Div Clin Epidemiol, Salt Lake City, UT USA
[5] NIDDK, Div Kidney Urol & Hematol Dis, Bethesda, MD USA
[6] Univ Chicago, Pritzker Sch Med, Dept Med, Hypertens Dis Unit, Chicago, IL 60637 USA
[7] Univ Illinois, Dept Med, Chicago, IL USA
[8] Morehouse Sch Med, Multidisciplinary Res Ctr, Atlanta, GA 30310 USA
[9] Emory Univ, Sch Med, Emory Ctr Hypertens & Renal Dis Res, Atlanta, GA USA
[10] Univ Miami, Miller Sch Med, Dept Med, Miami, FL 33136 USA
[11] Meharry Med Coll, Nashville, TN 37208 USA
[12] Vanderbilt Univ, Sch Med, Div Nephrol, Nashville, TN 37212 USA
[13] Vet Affairs San Diego Healthcare Syst, San Diego, CA USA
[14] Univ Calif San Diego, Dept Med, San Diego, CA 92103 USA
[15] Ohio State Univ, Med Ctr, Div Nephrol, Columbus, OH 43210 USA
[16] Univ Michigan, Div Cardiovasc Med, Ann Arbor, MI 48109 USA
[17] Harbor UCLA Med Ctr, Los Angeles Biomed Res Inst, Los Angeles, CA USA
[18] Univ Calif Los Angeles, Los Angeles, CA USA
[19] Los Angeles Cty Univ So Calif, Med Ctr, Los Angeles, CA USA
[20] Univ So Calif, Keck Sch Med, Div Nephrol, Los Angeles, CA 90033 USA
[21] Charles Drew Univ Med & Sci, Dept Internal Med, Los Angeles, CA USA
[22] Mt Sinai Sch Med, Dept Med, New York, NY USA
[23] Columbia Univ Coll Phys & Surg, Harlem Hosp Ctr, Dept Med, New York, NY 10032 USA
[24] Columbia Univ, New York, NY USA
[25] Univ Massachusetts, Sch Med, Cardiovasc Res Fdn, Worcester, MA USA
[26] Howard Univ, Washington, DC 20059 USA
[27] Howard Univ Hosp, Washington, DC USA
[28] Univ Alabama Birmingham, Div Nephrol, Birmingham, AL USA
[29] Univ Texas SW Med Ctr Dallas, Dept Med, Dallas, TX 75390 USA
基金
美国国家卫生研究院;
关键词
STAGE RENAL-DISEASE; AFRICAN-AMERICAN; PROGRESSION; PROTEINURIA; OUTCOMES; DESIGN; DIET;
D O I
10.1056/NEJMoa0910975
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
BACKGROUND In observational studies, the relationship between blood pressure and end-stage renal disease (ESRD) is direct and progressive. The burden of hypertension-related chronic kidney disease and ESRD is especially high among black patients. Yet few trials have tested whether intensive blood-pressure control retards the progression of chronic kidney disease among black patients. METHODS We randomly assigned 1094 black patients with hypertensive chronic kidney disease to receive either intensive or standard blood-pressure control. After completing the trial phase, patients were invited to enroll in a cohort phase in which the blood-pressure target was less than 130/80 mm Hg. The primary clinical outcome in the cohort phase was the progression of chronic kidney disease, which was defined as a doubling of the serum creatinine level, a diagnosis of ESRD, or death. Follow-up ranged from 8.8 to 12.2 years. RESULTS During the trial phase, the mean blood pressure was 130/78 mm Hg in the intensive-control group and 141/86 mm Hg in the standard-control group. During the cohort phase, corresponding mean blood pressures were 131/78 mm Hg and 134/78 mm Hg. In both phases, there was no significant between-group difference in the risk of the primary outcome (hazard ratio in the intensive-control group, 0.91; P = 0.27). However, the effects differed according to the baseline level of proteinuria (P = 0.02 for interaction), with a potential benefit in patients with a protein-to-creatinine ratio of more than 0.22 (hazard ratio, 0.73; P = 0.01). CONCLUSIONS In overall analyses, intensive blood-pressure control had no effect on kidney disease progression. However, there may be differential effects of intensive blood-pressure control in patients with and those without baseline proteinuria.
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收藏
页码:918 / 929
页数:12
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