Key result
Losartan reduced the risk of cardiovascular death, myocardial infarction, or stroke compared with atenolol (HR 0.86; 95% CI 0.76-0.98; P<0.05).
Why the study?
Does losartan-based treatment improve HDL cholesterol and reduce the composite of cardiovascular death, myocardial infarction, or stroke compared to atenolol-based treatment in patients with hypertension and left ventricular hypertrophy?
RCT (n=8,611)
randomized
Does losartan-based treatment improve HDL cholesterol and reduce the composite of cardiovascular death, myocardial infarction, or stroke compared to atenolol-based treatment in patients with hypertension and left ventricular hypertrophy?
Hazard Ratio: 0.86 (95% CI 0.76–0.98)
p-value: p=<0.05
Losartan blunts the decrease in HDL cholesterol compared to atenolol during antihypertensive treatment, which may partly explain its better cardiovascular outcomes.
Higher in-treatment HDL linked to fewer events independent of therapy; leaves open whether lipid effects should guide ARB vs beta-blocker selection in LVH.
OBJECTIVE: Beta-blockers and angiotensin II receptor blockers have different effects on lipids. METHODS: We examined lipid levels in the Losartan Intervention For Endpoint reduction in hypertension study and their impact on the primary composite endpoint of cardiovascular death, myocardial infarction, or stroke. We measured total and high-density lipoprotein cholesterol at baseline and annually during 4.8 years of losartan-based compared with atenolol-based treatment in 8611 patients with hypertension and left ventricular hypertrophy. RESULTS: Patients randomized to losartan-based or atenolol-based treatment had similar baseline total (6.04 +/- 1.12 vs. 6.05 +/- 1.13 mmol/l, NS) and high-density lipoprotein (HDL) cholesterol (1.50 +/- 0.44 vs. 1.49 +/- 0.44 mmol/l, NS). Total cholesterol decreased significantly but equally (-0.37 +/- 1.05 vs. -0.34 +/- 1.09 mmol/l, NS), whereas HDL cholesterol decreased less during the first 2 years in patients randomized to losartan compared with atenolol (-0.13 +/- 0.24 vs. -0.19 +/- 0.25 mmol/l) and remained higher each year (1.38, 1.37, 1.42, 1.47, and 1.48 mmol/l vs. 1.32, 1.30, 1.36, 1.40, and 1.42 mmol/l, all P < 0.001) independent of hydrochlorothiazide or statin treatment. In Cox regression analysis, baseline total cholesterol [hazard ratio (HR) = 1.08 (1.02-1.14) per mmol/l, P < 0.01], HDL cholesterol [HR = 0.56 (0.48-0.66) per mmol/l, P < 0.001], and treatment allocation [HR = 0.86 (0.76-0.98), P < 0.05] predicted composite endpoint independently. Using time-varying analyses, the predictive strength of HDL cholesterol was increased [HR = 0.36 (0.30-0.44) per mmol/l, P < 0.001], whereas that of total cholesterol [HR = 1.03 (0.97-1.09) per mmol/l, NS] and treatment allocation [HR = 0.91 (0.80-1.03), NS] were reduced. CONCLUSION: Losartan blunted the decrease in HDL cholesterol during antihypertensive treatment in the LIFE study. Higher intreatment HDL cholesterol was associated with fewer composite endpoints and may partly explain the better outcome of losartan-based treatment.
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Olsen et al. (2009) conducted an RCT in hypertension and left ventricular hypertrophy (n=8,611). Losartan vs. Atenolol was evaluated on Composite of cardiovascular death, myocardial infarction, or stroke (HR 0.86, 95% CI 0.76-0.98, p=<0.05). Losartan reduced the risk of cardiovascular death, myocardial infarction, or stroke compared with atenolol (HR 0.86; 95% CI 0.76-0.98; P<0.05).
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