Why the study?
Does nebivolol reduce blood pressure in African American patients with stage I or II hypertension?
Does nebivolol reduce blood pressure in African American patients with stage I or II hypertension?
Nebivolol monotherapy at doses of 5 mg or higher is effective and well-tolerated for reducing blood pressure in hypertensive African American patients, a population that typically responds poorly to standard beta-blockers.
Supports nebivolol ≥5 mg for BP reduction in African American hypertensives; extends beta-blocker efficacy data to a population with historically limited response.
Hypertensive African Americans often respond poorly to beta-blocker monotherapy, compared with whites. There is evidence, however, that suggests that this response may be different if beta-blockers with vasodilating effects are used. This 12-week, multi-center, double-blind, randomized placebo-controlled study assessed the antihypertensive efficacy and safety of nebivolol, a cardioselective, vasodilating beta1-blocker, at doses of 2.5, 5, 10, 20, or 40 mg once daily in 300 African American patients with stage I or II hypertension (mean sitting diastolic blood pressure [SiDBP] > or =95 mm Hg and < or =109 mm Hg). The primary efficacy end point was the baseline-adjusted change in trough mean SiDBP. After 12 weeks, nebivolol significantly reduced least squares mean SiDBP (P< or =.004) at all doses of 5 mg and higher and sitting systolic blood pressure (P< or =.044) at all doses 10 mg and higher, compared with placebo. The drug was safe and well-tolerated, with no significant difference in the incidence of adverse events compared with placebo. Nebivolol monotherapy provides antihypertensive efficacy, with few significant adverse effects, in hypertensive African Americans.
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Saunders et al. (2007) studied this question.
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