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Design of the LIFE study
The primary objective of the LIFE study was to
test the long-term effects of once-daily losartan-based
treatment compared to a well-documented atenolol-based
treatment on cardiovascular death and disease.
It included patients with hypertension and enlarged
hearts because they are known to be at greater
risk for the cardiovascular events of hypertension
and, as such, are a very important population
to study in hypertension outcomes trials. An enlarged
heart, or left ventricular hypertrophy (LVH),
is a common result of longer-term hypertension.
Atenolol is a proven standard for the treatment
of hypertension and is known for its cardiovascular
benefits. As a result it is the most widely used
beta-blocker to treat hypertension.
In this double-blind, randomized, parallel-group
design, 9,193 men and women aged 55-80 years (average
67 years) with essential hypertension (sitting
blood pressure 160-200/95-115 mmHg, average 174/98
mmHg) and ECG-documented LVH (enlarged heart),
were assigned once daily losartan- or atenolol-based
antihypertensive therapy. Patient enrollment began
in 1995 in 945 centres in 7 countries which included
Denmark (n=1,391), Finland (n=1,485), Iceland
(n=133), Norway (n=1,415), Sweden (n=2,245), UK
(n=817) and USA (n=1,707). Completed in 2001,
LIFE is one of the largest hypertension trials
ever conducted.
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