Key result
Higher bopindolol doses show no additional diastolic blood pressure reduction over 0.5 mg.
Why the study?
The optimal antihypertensive dose of bopindolol was uncertain and previous studies suggested higher doses without parallel randomized groups.
RCT (n=115)
Double-blind
parallel groups
p-value: p=0.1
Supports lowest effective bopindolol dosing in hypertension; challenges linear dose-response assumptions for beta-blockers.
To determine the optimal antihypertensive dose of bopindolol, we performed a randomized double-blind study in parallel groups. After 15 days of placebo single-blind, 115 hypertensive patients received daily for 28 days one of 4 doses: 0 mg (placebo), 0.5 mg, 1.0 mg, 2.0 mg. The reduction of supine diastolic blood pressure (BP) did not exhibit the pattern of a dose-effect relationship. The effect of 0.5 mg belonged to the plateau of the dose-effect curve (P = 0.1, analysis of variance). The reduction of heart rate (HR) followed a typical dose-effect curve, with a plateau beginning with 1 mg (P = 0.02). A trend toward an increase in the incidence of side-effects with dosage was observed (P = 0.3). Thus, the optimal antihypertensive dose may be 0.5 mg or less. Previous studies not using parallel randomized groups suggested an antihypertensive dose ranging from 2 to 4 mg. This study confirms that the dose-effect curves of beta blockers on HR and BP are dissociated. The dose-effect curve of HR seems unsuitable for assessing the optimal antihypertensive dose of a beta blocker.
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Moleur et al. (1988) conducted an RCT in Moderate hypertension (n=115). Bopindolol vs. Placebo (0 mg) was evaluated on Reduction of supine diastolic blood pressure (p=0.1). Bopindolol demonstrated no continuous dose-effect relationship for diastolic blood pressure reduction across 0.5 to 2.0 mg doses, suggesting an optimal antihypertensive dose of 0.5 mg or less (P=0.1).
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