Hermida Ramón C, Calvo Carlos, Ayala Diana E, Fernández José R, Covelo Manuel, Mojón Artemio, López José E
Bioengineering and Chronobiology Laboratories, University of Vigo, Campus Universitario, Vigo and Hypertension and Vascular Risk Unit, Hospital Clínico Universitario, Santiago de Compostela, Spain.
J Hypertens. 2005 Oct;23(10):1913-22. doi: 10.1097/01.hjh.0000182522.21569.c5.
Previous results have indicated that valsartan administration at bedtime, as opposed to upon wakening, may improve the diurnal: nocturnal ratio of blood pressure without loss in 24-h coverage and efficacy.
To investigate the administration time-dependent antihypertensive efficacy of valsartan in non-dipper patients.
We studied 148 non-dipper patients with grade 1-2 essential hypertension, aged 53.0+/-12.6 years, who were randomly assigned to receive valsartan (160 mg/day) as a monotherapy either on awakening or at bedtime. Blood pressure was measured every 20 min during the day and every 30 min at night for 48 consecutive hours before and after 3 months of treatment. Physical activity was simultaneously monitored every minute by wrist actigraphy to accurately calculate the diurnal and nocturnal means of blood pressure on a per subject basis.
The significant blood pressure reduction after 3 months of valsartan (P<0.001) was similar for both treatment times (13.1 and 8.5 mmHg reduction in the 24-h mean of systolic and diastolic blood pressure with morning administration; 14.7 and 10.3 mmHg with bedtime administration; P>0.126 for treatment-time effect). The diurnal: nocturnal ratio of blood pressure was significantly increased only when valsartan was administered before bedtime, which resulted in 75% of the patients in this group reverting to dippers, a significant increase in the percentage of patients with controlled blood pressure over 24 h, and a reduction in urinary albumin excretion.
In non-dipper hypertensive patients, dosing time with valsartan should be chosen at bedtime, for improved efficacy during the nocturnal resting hours, as well as the potential associated reduction in cardiovascular risk.
先前的研究结果表明,与晨起服用相比,缬沙坦在睡前服用可改善血压的昼夜比值,且不影响24小时血压控制及疗效。
探讨缬沙坦在非勺型高血压患者中给药时间依赖性的降压疗效。
我们研究了148例年龄为53.0±12.6岁的1-2级原发性高血压非勺型患者,这些患者被随机分配为晨起或睡前接受缬沙坦单药治疗(160mg/天)。治疗3个月前后,连续48小时白天每20分钟、夜间每30分钟测量一次血压。同时通过手腕活动记录仪每分钟监测一次身体活动,以准确计算每位受试者的昼夜平均血压。
缬沙坦治疗3个月后血压显著降低(P<0.001),两种给药时间的降压效果相似(晨起给药时24小时收缩压和舒张压平均值分别降低13.1和8.5mmHg;睡前给药时分别降低14.7和10.3mmHg;治疗时间效应P>0.126)。仅当睡前服用缬沙坦时,血压的昼夜比值显著升高,该组75%的患者转变为勺型血压,24小时血压控制良好的患者百分比显著增加,尿白蛋白排泄减少。
对于非勺型高血压患者,应选择在睡前服用缬沙坦,以提高夜间休息时的疗效,并可能降低心血管风险。