In a double-masked, randomized, parallel-group trial (LIFE) 1 1 195 diabetic patients (of the total of 9 193) aged 55 - 88 years with electrocardiographically ascertained LVH received either losartan ad 100 mg/d or atenolol 100 mg/d. Most patients also received hydrochlorothiazide. The primary composite end point (death, myocardial infarction, or stroke) occurred in 103 losartan and in 139 atenolol patients (RR 0.76, 95% CI 0.58 to 0.98). 38 and 61 patients in the losartan and atenolol groups, respectively, died from cardiovascular disease (RR 0.63, 95% CI 0.42 to 0.95). Mortality from all causes was 63 and 104 in losartan and atenolol groups (RR 0.61, 95% CI 0.45 to 0.84).
Comment: The quality of evidence is downgraded by imprecise results (few outcome events).
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