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Sökning: WFRF:(Lindholm Lars H.) > (2005-2009) > The effect of losar...

The effect of losartan versus atenolol on cardiovascular morbidity and mortality in patients with hypertension taking aspirin: the Losartan Intervention for Endpoint Reduction in hypertension (LIFE) study

Fossum, E. (författare)
Moan, A. (författare)
Kjeldsen, S. E. (författare)
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Devereux, R. B. (författare)
Julius, S. (författare)
Snapinn, S. M. (författare)
Edelman, J. M. (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)
Dahlöf, Björn, 1953 (författare)
Gothenburg University,Göteborgs universitet,Hjärt-kärlinstitutionen,Cardiovascular Institute
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 (creator_code:org_t)
Elsevier BV, 2005
2005
Engelska.
Ingår i: J Am Coll Cardiol. - : Elsevier BV. - 0735-1097. ; 46:5, s. 770-5
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
Stäng  
  • OBJECTIVES: We conducted a subgroup analysis in the Losartan Intervention For Endpoint reduction in hypertension (LIFE) study to determine whether aspirin interacted with the properties of losartan, an angiotensin-II receptor antagonist. BACKGROUND: Negative interactions between angiotensin-converting enzyme inhibitors and aspirin have been reported. There are no data reported from clinical trials about possible interactions between angiotensin-II receptor antagonists and aspirin. METHODS: The LIFE study assigned 9,193 patients with hypertension and left ventricular hypertrophy (LVH) to losartan- or atenolol-based therapy for a mean of 4.7 years, with 1,970 (21.4%) taking aspirin at baseline. The primary composite end point (CEP) included cardiovascular death, stroke, and myocardial infarction (MI). The present cohort was stratified by aspirin use at baseline. RESULTS: Blood pressures were reduced similarly in the losartan with aspirin (n = 1,004) and atenolol with aspirin (n = 966) groups. The CEP was reduced by 32% (95% confidence interval 0.55 to 0.86, p = 0.001) with losartan with aspirin compared to atenolol with aspirin, adjusted for Framingham risk score and LVH. The test for treatment versus aspirin interaction, excluding other covariates, was significant for the CEP (p = 0.016) and MI (p = 0.037). CONCLUSIONS: There was a statistical interaction between treatment and aspirin in the LIFE study, with significantly greater reductions for the CEP and MI with losartan in patients using aspirin than in patients not using aspirin at baseline. Further studies are needed to clarify whether this represents a pharmacologic interaction or a selection by aspirin use of patients more likely to respond to losartan treatment.

Nyckelord

Adrenergic beta-Antagonists/adverse effects/*therapeutic use
Aged
Angiotensin II Type 1 Receptor Blockers/adverse effects/*therapeutic use
Aspirin/adverse effects/*therapeutic use
Atenolol/adverse effects/*therapeutic use
Drug Interactions
Drug Therapy
Combination
Female
Humans
Hypertension/complications/*drug therapy
Hypertrophy
Left Ventricular/complications/*drug therapy
Losartan/adverse effects/*therapeutic use
Male
Treatment Outcome
Adrenergic beta-Antagonists/adverse effects/*therapeutic use

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