Cardiovascular risk reduction in hypertensive black patients with left ventricular hypertrophy -: The LIFE study

被引:87
|
作者
Julius, S
Alderman, MH
Beevers, G
Dahlöf, B
Devereux, RB
Douglas, JG
Edelman, JM
Harris, KE
Kjeldsen, SE
Nesbitt, S
Randall, OS
Wright, JT
机构
[1] Univ Michigan, Med Ctr, Dept Internal Med, Div Hypertens,Taubman Ctr 3918, Ann Arbor, MI 48109 USA
[2] Howard Univ Hosp, Gen Clin Res Ctr, Washington, DC USA
[3] Univ Texas, SW Med Ctr, Dept Internal Med, Div Hypertens, Dallas, TX USA
[4] Ullevaal Univ Hosp, Dept Cardiol, Oslo, Norway
[5] Univ Michigan, Dept Internal Med, Ann Arbor, MI 48109 USA
[6] Merck & Co Inc, West Point, PA USA
[7] Case Western Reserve Univ, Div Hypertens, Cleveland, OH 44106 USA
[8] Cornell Med Ctr, Div Cardiol, New York, NY USA
[9] Sahlgrens Univ Hosp, Dept Med, Ostra, S-41345 Gothenburg, Sweden
[10] City Hosp, Birmingham, W Midlands, England
[11] Albert Einstein Coll Med, Bronx, NY 10467 USA
关键词
D O I
10.1016/j.jacc.2003.11.029
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
OBJECTIVES We report on a subanalysis of the effects of losartan and atenolol on cardiovascular events in black patients in the Losartan Intervention For Endpoint reduction in hypertension (LIFE) study. BACKGROUND The LIFE study compared losartan-based to atenolol-based therapy in 9,193 hypertensive patients with left ventricular hypertrophy (LVH). Overall, the risk of the primary composite end point (cardiovascular death, stroke, myocardial infarction) was reduced by 13% (p = 0.021) with losartan, with similar blood pressure (BP) reduction in both treatment groups. There was a suggestion of interaction between ethnic background and treatment (p = 0.057). METHODS Exploratory analyses were performed that placed LIFE study patients into black (n = 533) and non-black (n = 8,660) categories, overall, and in the U.S. (African American [n = 523]; non-black [n = 1,184]). RESULTS A significant interaction existed between the dichotomized groups (black/non-black) and treatment (p = 0.005); a test for qualitative interaction was also significant (p = 0.016). The hazard ratio (losartan relative to atenolol) for the primary end point favored atenolol in black patients (1.666 [95% confidence interval (CI) 1.043 to 2.661]; p = 0.033) and favored losartan in non-blacks (0.829 [95% CI 0.733 to 0.938]; p = 0.003). In black patients, BP reduction was similar in both groups, and regression of electrocardiographic-LVH was greater with losartan. CONCLUSIONS Results of the subanalysis are sufficient to generate the hypothesis that black patients with hypertension and LVH might not respond as favorably to losartan-based treatment as non-black patients with respect to cardiovascular outcomes, and do not support a recommendation for losartan as a first-line treatment for this purpose. The subanalysis is limited by the relatively small number of events. (C) 2004 by the American College of Cardiology Foundation.
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收藏
页码:1047 / 1055
页数:9
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