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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

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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.

Abbreviations and Acronyms

BP
blood pressure
CI
confidence interval
ECG
electrocardiogram
LIFE
Losartan Intervention For Endpoint reduction in hypertension
LVH
left ventricular hypertrophy
MI
myocardial infarction
RR
relative risk

Cited by (0)

Merck and Co., Inc., has supported the trial by an unrestricted grant and has reviewed the manuscript. Dr. Fossum has received speakers’ honoraria from Merck. Drs. Kjeldsen, Devereux, Julius, de Faire, Fyhrquist, Ibsen, Lederballe-Pedersen, Lindholm, Nieminen, Omvik, Oparil, Wedel, and Dahlöf are members of the LIFE Steering Committee and have received grant support from Merck and Co., Inc., the sponsor of the LIFE study. Drs. Moan, Snapinn, Edelman, and Kristianson are or have been employees of Merck and may own stock or stock options in the company. The presentation of data is the intellectual property of the LIFE Steering Committee.