Why the study?
Does cilnidipine 10 mg/day improve blood pressure and autonomic functions in patients with mild-to-moderate hypertension?
Does cilnidipine 10 mg/day improve blood pressure and autonomic functions in patients with mild-to-moderate hypertension?
Cilnidipine effectively lowers blood pressure and improves autonomic function without causing orthostatic hypotension or reflex tachycardia in patients with mild-to-moderate hypertension.
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Cilnidipine was associated with BP reduction in mild-to-moderate hypertension; hypothesis-generating for autonomic effects pending RCTs.
The current study was conducted to examine the effects of cilnidipine, a dual L/N-type calcium channel blocker, on blood pressure, pulse rate, and autonomic functions in patients with mild-to-moderate hypertension. Sixteen patients with mild-to-moderate hypertension (8 males and 8 females; 44-72 years of age) were treated with cilnidipine (10 mg/day) for 3 months. Before and after the treatment, the following measurements were conducted; beat-to-beat blood pressure during late phase II and overshoot phase of the Valsalva maneuver, the Valsalva ratio, heart rate response to deep breathing, systolic and diastolic blood pressure, and pulse rate. The head-up tilt test was also performed before and after the treatment. Cilnidipine significantly decreased either the systolic or diastolic blood pressure from 151 +/- 15 mmHg to 129 +/- 14 mmHg or 84 +/- 11 mmHg to 71 +/- 9 mmHg, respectively. For pulse rate, there were no significant changes during therapy. Beat-to-beat blood pressure during late phase II and overshoot phase of the Valsalva maneuver indicated significant improvements in both figures. The heart rate response to deep breathing and the Valsalva ratio indicated no significant differences during therapy. Before and after the treatment, no orthostatic hypotension was observed during the head-up tilt test. The current study revealed that cilnidipine significantly decreases blood pressure with improving autonomic functions while having no adverse effects on heart rate response and pulse rate.
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Kai et al. (2009) studied this question.
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