Does albuminuria predict cardiovascular outcome on treatment with losartan versus atenolol in hypertension with left ventricular hypertrophy?: A LIFE substudy

被引:96
|
作者
Ibsen, H
Wachtell, K
Olsen, MH
Borch-Johnsen, K
Lindholm, LH
Mogensen, CE
Dahlöf, B
Devereux, RB
de Faire, U
Fyhrquist, F
Julius, S
Kjeldsen, SE
Lederballe-Pedersen, O
Nieminen, MS
Omvik, P
Oparil, S
Wan, Y
机构
[1] Glostrup Univ Hosp, Glostrup, Denmark
[2] Cornell Univ, Weill Med Coll, New York, NY USA
[3] Steno Diabet Ctr, DK-2820 Gentofte, Denmark
[4] Univ Umea Hosp, S-90185 Umea, Sweden
[5] Arhus Univ Hosp, Aarhus, Denmark
[6] Sahlgrens Univ Hosp, S-41345 Gothenburg, Sweden
[7] Stockholm Univ, Karolinska Hosp, S-10691 Stockholm, Sweden
[8] Univ Helsinki, Cent Hosp, Helsinki, Finland
[9] Univ Michigan, Ann Arbor, MI 48109 USA
[10] Univ Oslo, Ullevaal Hosp, N-0407 Oslo, Norway
[11] Univ Bergen, Haukeland Hosp, N-5021 Bergen, Norway
[12] Univ Alabama, Birmingham, AL USA
[13] Merck Res Labs, W Point, PA USA
关键词
albuminuria; hypertension; left ventricular hypertrophy; losartan; atenolol; LIFE study; morbidity and mortality; stroke;
D O I
10.1097/00004872-200409000-00026
中图分类号
R6 [外科学];
学科分类号
1002 ; 100210 ;
摘要
Objectives To examine a possible relationship between baseline albuminuria and effect of losartan versus atenolol on cardiovascular (CV) events in hypertensive patients with left ventricular hypertrophy, the effect of losartan versus atenolol on albuminuria, and whether the benefits of losartan versus atenolol could be explained by influence of losartan on albuminuria. Design Double-blind, randomized, controlled trial of 4.8 years. Setting Out-patient setting. Patients A total of 8206 with hypertension and left ventricular hypertrophy. Interventions Losartan or atenolol, supplemented with diuretics and/or calcium antagonists to reach blood pressure < 140/90 mmHg Main outcome measures The urine albumin/creatinine ratio, and the primary composite endpoint (CEP) of CV death, myocardial infarction, and stroke. Results The blood pressure was reduced similarly on losartan (30.2/16.6 mmHg) versus atenolol (29.1/16.8 mmHg). The risk of a primary CEP increased linearly from the lowest to the highest decile of baseline albuminuria. The benefits of losartan versus atenolol for the primary CEP and for stroke tended to be more pronounced among patients above the median value for baseline albuminuria (urine albumin/creatinine ratio, 1.28 mg/mmol). The decrease in albuminuria was significantly greater with losartan versus atenolol throughout the study (a decrease from baseline to year 2 of 33% losartan versus 25% atenolol). One-fifth of the difference in favor of losartan on the primary CEP was explained by the greater reduction in albuminuria on losartan. Conclusions Baseline albuminuria is a powerful risk factor for CV events. Baseline albuminuria did not identify the group of patients with greatest benefit on losartan versus atenolol in LIFE. Reduction in albuminuria explained one-fifth of the benefits of losartan versus atenolol. (C) 2004 Lippincott Williams Wilkins.
引用
收藏
页码:1805 / 1811
页数:7
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