HOPE-3 Trial design: Patients without known cardiovascular disease, and with an intermediate risk of cardiovascular events, were randomized in a 2 x 2.

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HOPE-3 Trial design: Patients without known cardiovascular disease, and with an intermediate risk of cardiovascular events, were randomized in a 2 x 2 factorial design to either cholesterol lowering or BP lowering or both. Patients were followed for a median of 5.6 years. Results (p = 0.002) (p = 0.40) Primary endpoint: CV death/MI/stroke Rosuvastatin vs. placebo: 3.7% vs. 4.8%, HR 0.76, 95% CI 0.64-0.91, p = 0.002 Candesartan + HCTZ vs. placebo: 4.1% vs. 4.4%, HR 0.93, 95% CI 0.79-1.1, p = 0.40 Rosuvastatin + candesartan + HCTZ vs. placebo: 3.6% vs. 5.0%, HR 0.71, 95% CI 0.56-0.9, p = 0.005 30 30 20 20 % % Conclusions 10 10 3.7 4.8 4.1 4.4 Fixed-dose treatment with low-dose statin therapy, but not BP agents, was superior to placebo in reducing long-term cardiovascular events in an intermediate-risk population; combination group with benefits similar to statin arm Provides support for a risk-based approach to the management of patients with hyperlipidemia and hypertension Primary endpoint (CV death/MI/stroke) Rosuva 10 n = 6,361 Placebo n = 6,344 Cande 16 + HCTZ 12.5 n = 6,356 Placebo n = 6,349 HOPE-3 Investigators. N Engl J Med 2016;Apr 2:[Epub]