White William B, Sica Domenic A, Calhoun David, Mansoor George A, Anders Robert J
Section of Hypertension and Clinical Pharmacology, University of Connecticut School of Medicine, Farmington, Conn 06030-3940, USA.
Am Heart J. 2002 Oct;144(4):657-65. doi: 10.1067/mhj.2002.124866.
Therapeutic agents for the treatment of hypertension may differ in their efficacy during the early-morning period, a time when both morbid and mortal cardiovascular events are increased compared with other times of the day.
We studied the effects of a chronotherapeutic delivery system of verapamil (controlled-onset extended release [COER]-24 system) dosed at bedtime versus conventional morning administration of both enalapril and losartan on the blood pressure (BP), heart rate, and the heart rate systolic BP product during the first 4 hours after awakening in a placebo-controlled, forced-titration trial. There were 357 men and women enrolled in the trial with an untreated sitting diastolic BP of 95 to 114 mm Hg and ambulatory daytime diastolic BP > or =85 mm Hg. Patients were randomized to either COER-verapamil hydrochloride each evening (240 mg titrated to 360 mg), enalapril each morning (10 mg titrated to 20 mg), losartan each morning (50 mg titrated to 100 mg), or placebo. Early morning assessments of BP, heart rate, and the heart rate systolic BP product were performed by use of 24-hour ambulatory recordings after 4 weeks (low dose) and 8 weeks (high dose) of therapy.
Results were similar at weeks 4 and 8 for all treatment groups except that the magnitude of change was greater at week 8. After 8 weeks of treatment, reductions in early morning BP by COER-verapamil were significantly greater (-15/-10 mm Hg) than enalapril (-9/-7 mm Hg, P <.01) and losartan (-8/-5 mm Hg, P <.001). COER-verapamil also led to greater reductions in morning heart rate, the rate-pressure product, and the rate-of-rise of BP compared with the other 2 active treatment groups. Reductions in mean 24-hour BP were greater in patients treated with COER-verapamil compared with placebo and losartan, and similar to reductions in patients treated with enalapril.
Bedtime administration of an agent designed to parallel the circadian rhythm of BP and heart rate led to significantly greater early morning hemodynamic effects compared with other conventional once-daily antihypertensive agents dosed in the morning.
治疗高血压的药物在清晨时段的疗效可能有所不同,与一天中的其他时段相比,此时心血管疾病的发病和死亡事件均有所增加。
在一项安慰剂对照、强制滴定试验中,我们研究了睡前服用维拉帕米的时辰治疗给药系统(控释起效缓释[COER]-24系统)与依那普利和氯沙坦早晨常规给药相比,对觉醒后最初4小时内的血压(BP)、心率以及心率收缩压乘积的影响。共有357名男性和女性参与该试验,其未治疗时的坐位舒张压为95至114毫米汞柱,日间动态舒张压≥85毫米汞柱。患者被随机分为每晚服用COER-盐酸维拉帕米(240毫克滴定至360毫克)、每天早晨服用依那普利(10毫克滴定至20毫克)、每天早晨服用氯沙坦(50毫克滴定至100毫克)或安慰剂。在治疗4周(低剂量)和8周(高剂量)后,通过24小时动态记录进行清晨血压、心率以及心率收缩压乘积的评估。
除了变化幅度在第8周更大外,所有治疗组在第4周和第8周的结果相似。治疗8周后,COER-维拉帕米使清晨血压的降低幅度(-15/-10毫米汞柱)显著大于依那普利(-9/-7毫米汞柱,P<.01)和氯沙坦(-8/-5毫米汞柱,P<.001)。与其他两个活性治疗组相比,COER-维拉帕米还使早晨心率、率压乘积以及血压上升速率有更大幅度的降低。与安慰剂和氯沙坦相比,服用COER-维拉帕米的患者24小时平均血压降低幅度更大,与服用依那普利的患者相似。
与其他早晨服用的常规每日一次降压药物相比,睡前服用一种旨在与血压和心率昼夜节律同步的药物可产生显著更大的清晨血流动力学效应。