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Angiotensin II receptor blockade reduces new-onset atrial fibrillation and subsequent stroke compared to atenolol: the Losartan Intervention For End Point Reduction in Hypertension (LIFE) study

Wachtell, K. (författare)
Lehto, M. (författare)
Gerdts, E. (författare)
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Olsen, M. H. (författare)
Hornestam, Björn, 1957- (författare)
Göteborgs universitet, Hjärt-kärlinstitutionen
Dahlöf, Björn, 1953- (författare)
Göteborgs universitet, Hjärt-kärlinstitutionen
Ibsen, H. (författare)
Julius, S. (författare)
Kjeldsen, S. E. (författare)
Lindholm, L. H. (författare)
Nieminen, M. S. (författare)
Devereux, R. B. (författare)
visa färre...
Göteborgs universitet Sahlgrenska akademin. Hjärt-kärlinstitutionen. 
Umeå universitet Medicinsk fakultet. Folkhälsa och klinisk medicin. Allmänmedicin. 
2005
Engelska.
Ingår i: J Am Coll Cardiol. - 0735-1097. ; 45:5, s. 712-9
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
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  • OBJECTIVES: This study was designed to evaluate whether different antihypertensive treatment regimens with similar blood pressure reduction have different effects on new-onset atrial fibrillation (AF). BACKGROUND: It is unknown whether angiotensin II receptor blockade is better than beta-blockade in preventing new-onset AF. METHODS: In the Losartan Intervention For Endpoint reduction in hypertension (LIFE) study 9,193 hypertensive patients and patients with electrocardiogram-documented left ventricular hypertrophy were randomized to once-daily losartan- or atenolol-based antihypertensive therapy. Electrocardiograms were Minnesota coded centrally, and 8,851 patients without AF by electrocardiogram or history, who were thus at risk of developing AF, were followed for 4.8 +/- 1.0 years. RESULTS: New-onset AF occurred in 150 patients randomized to losartan versus 221 to atenolol (6.8 vs. 10.1 per 1,000 person-years; relative risk 0.67, 95% confidence interval [CI] 0.55 to 0.83, p < 0.001) despite similar blood pressure reduction. Patients receiving losartan tended to stay in sinus rhythm longer (1,809 +/- 225 vs. 1,709 +/- 254 days from baseline, p = 0.057) than those receiving atenolol. Moreover, patients with new-onset AF had two-, three- and fivefold increased rates, respectively, of cardiovascular events, stroke, and hospitalization for heart failure. There were fewer composite end points (n = 31 vs. 51, hazard ratio = 0.60, 95% CI 0.38 to 0.94, p = 0.03) and strokes (n = 19 vs. 38, hazard ratio = 0.49, 95% CI 0.29 to 0.86, p = 0.01) in patients who developed new-onset AF in the losartan compared to the atenolol treatment arm of the study. Furthermore, Cox regression analysis showed that losartan (21% risk reduction) and new-onset AF both independently predicted stroke even when adjusting for traditional risk factors. CONCLUSIONS: Our novel finding is that new-onset AF and associated stroke were significantly reduced by losartan- compared to atenolol-based antihypertensive treatment with similar blood pressure reduction.

Ämnesord

MEDICIN OCH HÄLSOVETENSKAP  (hsv//swe)
MEDICAL AND HEALTH SCIENCES  (hsv//eng)

Nyckelord

MEDICIN
MEDICINE
Adrenergic beta-Antagonists/*therapeutic use
Aged
Aged
80 and over
Angiotensin II Type 1 Receptor Blockers/*therapeutic use
Atenolol/*therapeutic use
Atrial Fibrillation/*drug therapy/mortality
Cause of Death
Cerebrovascular Accident/*drug therapy/mortality
Double-Blind Method
Female
Humans
Hypertension/*drug therapy/mortality
Hypertrophy
Left Ventricular/*drug therapy/mortality
Losartan/*therapeutic use
Male
Middle Aged
Prospective Studies
Recurrence/prevention & control
Risk Factors
Survival Rate
Aged; 80 and over
Hypertrophy; Left Ventricular/*drug therapy/mortality
Stroke/*drug therapy/mortality

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