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Alcohol consumption and cardiovascular risk in hypertensives with left ventricular hypertrophy: the LIFE study

Reims, H. M. (författare)
Kjeldsen, S. E. (författare)
Brady, W. E. (författare)
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Dahlöf, Björn, 1953 (författare)
Gothenburg University,Göteborgs universitet,Hjärt-kärlinstitutionen,Cardiovascular Institute
Devereux, R. B. (författare)
Julius, S. (författare)
Beevers, G. (författare)
de Faire, U. (författare)
Karolinska Institutet
Fyhrquist, F. (författare)
Ibsen, H. (författare)
Kristianson, K. (författare)
Karolinska Institutet
Lederballe-Pedersen, O. (författare)
Lindholm, Lars H (författare)
Umeå universitet,Allmänmedicin
Nieminen, M. S. (författare)
Omvik, P. (författare)
Oparil, S. (författare)
Wedel, H. (författare)
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 (creator_code:org_t)
Springer Science and Business Media LLC, 2004
2004
Engelska.
Ingår i: J Hum Hypertens. - : Springer Science and Business Media LLC. - 0950-9240 .- 1476-5527. ; 18:6, s. 381-9
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
Stäng  
  • The Losartan Intervention For End point reduction in hypertension (LIFE) study showed superiority of losartan over atenolol for reduction of composite risk of cardiovascular death, stroke, and myocardial infarction in hypertensives with left ventricular hypertrophy. We compared hazard ratios (HR) in 4287 and 685 participants who reported intakes of 1-7 and >8 drinks/week at baseline, respectively, with those in 4216 abstainers, adjusting for gender, age, smoking, exercise, and race. Within categories, clinical baseline characteristics, numbers randomized to losartan and atenolol, and blood pressure (BP) lowering were similar on the drug regimens. Overall BP control (<140/90 mmHg) at end of follow-up was similar in the categories. Composite end point rate was lower with 1-7 (24/1000 years; HR 0.87, P<0.05) and >8 drinks/week (26/1000 years; HR 0.80, NS) than in abstainers (27/1000 years). Myocardial infarction risk was reduced in both drinking categories (HR 0.76, P<0.05 and HR 0.29, P<0.001, respectively), while stroke risk tended to increase with >8 drinks/week (HR 1.21, NS). Composite risk was significantly reduced with losartan compared to atenolol only in abstainers (HR 0.81 95% confidence interval, CI (0.68, 0.96), P<0.05), while benefits for stroke risk reduction were similar among participants consuming 1-7 drinks/week (HR 0.73, P<0.05) and abstainers (HR 0.72, P<0.01). Despite different treatment benefits, alcohol-treatment interactions were nonsignificant. In conclusion, moderate alcohol consumption does not change the marked stroke risk reduction with losartan compared to atenolol in high-risk hypertensives. Alcohol reduces the risk of myocardial infarction, while the risk of stroke tends to increase with high intake.

Nyckelord

Aged
Aged
80 and over
Alcohol Drinking/*adverse effects
Antihypertensive Agents/therapeutic use
Atenolol/therapeutic use
Cerebrovascular Accident/*etiology/*prevention & control
Female
Humans
Hypertension/complications/drug therapy
Hypertrophy
Left Ventricular/complications/drug therapy
Losartan/therapeutic use
Male
Middle Aged
Myocardial Infarction/*etiology/*prevention & control
Risk Factors
Treatment Outcome
Aged

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