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硝苯地平控释片国际研究中高血压治疗以干预为目标的24小时动态血压监测(INSIGHT)

Twenty-four hour ambulatory blood pressure in the International Nifedipine GITS Study Intervention as a Goal in Hypertension Treatment (INSIGHT).

作者信息

Mancia Giuseppe, Omboni Stefano, Parati Gianfranco

机构信息

Clinica Medica, Dipartimento di Medicina Clinica, Prevenzione e Biotecnologie Sanitarie, Università di Milano-Bicocca, Ospedale San Gerardo, Monza, Italy.

出版信息

J Hypertens. 2002 Mar;20(3):545-53. doi: 10.1097/00004872-200203000-00032.

Abstract

OBJECTIVES

The International Nifedipine GITS Study Intervention as a Goal in Hypertension Treatment (INSIGHT) showed, by means of office blood pressure measurements, that long-term treatment with nifedipine GITS is as effective as diuretics in preventing cardiovascular and cerebrovascular complications. However, since office blood pressure measurements reflect to a limited extent blood pressure outside the office, a side-arm INSIGHT study in which patients underwent both office measurement and 24 h ambulatory blood pressure monitoring was also performed.

DESIGN AND METHODS

The study had a randomized, double-blind, parallel group design. After 4 weeks of placebo, mild-to-moderate essential hypertensive patients were randomized to nifedipine GITS 30 mg or amiloride 2.5 + hydrochlorothiazide 5 mg for 3.1 years. Dose titration was performed by dose doubling and addition of atenolol 25-50 mg or enalapril 5-10 mg, or other drugs when needed. Analysis was carried out by intention-to-treat and included computation of 24 h, day and night ambulatory blood pressure and heart rate values. Additional analyses included computation of the trough-to-peak ratio and the smoothness index (the ratio between the average of the 24-hourly blood pressure reductions after treatment and its standard deviation).

RESULTS

A total of 151 patients were recruited and 149 were valid for analysis: 78 patients had 24 h ambulatory recordings both at baseline and during treatment and 134 during treatment. Office, 24 h and day and night blood pressures were all significantly and similarly reduced by both treatments. Office and ambulatory heart rate was left unchanged by diuretics, while it was slightly reduced by nifedipine. Median trough-to-peak ratios were always > 0.5 and superimposable between the two treatment groups. Similarly, smoothness indices of systolic and diastolic blood pressures were comparably high for nifedipine and diuretics, thus demonstrating a similar well-balanced antihypertensive response to both drugs. No significant differences were observed between the two treatment groups in the number of cardiovascular events (17 in the nifedipine-based and 26 in the diuretics-based treatment group).

CONCLUSIONS

In the INSIGHT study, the long-term antihypertensive effect on 24 h blood pressure and the cardiovascular protection of nifedipine was similar to that of diuretics.

摘要

目的

硝苯地平控释片国际高血压治疗研究(INSIGHT)通过诊室血压测量表明,硝苯地平控释片长期治疗在预防心脑血管并发症方面与利尿剂效果相当。然而,由于诊室血压测量在一定程度上仅反映诊室以外的血压情况,因此还开展了一项INSIGHT辅助研究,让患者同时接受诊室测量和24小时动态血压监测。

设计与方法

该研究采用随机、双盲、平行组设计。在服用4周安慰剂后,轻度至中度原发性高血压患者被随机分为两组,分别接受30毫克硝苯地平控释片或2.5毫克阿米洛利+5毫克氢氯噻嗪治疗3.1年。通过双倍剂量给药以及在需要时加用25 - 50毫克阿替洛尔或5 - 10毫克依那普利或其他药物进行剂量滴定。采用意向性分析,计算24小时、白天和夜间的动态血压及心率值。额外分析包括计算谷峰比和平滑指数(治疗后24小时血压降低平均值与其标准差的比值)。

结果

共招募了151名患者,149名患者可进行有效分析:78名患者在基线和治疗期间均有24小时动态血压记录,134名患者在治疗期间有记录。两种治疗方法均使诊室、24小时以及白天和夜间血压显著且相似地降低。利尿剂治疗后诊室和动态心率未改变,而硝苯地平使其略有降低。两个治疗组的中位谷峰比均始终>0.5且相互重叠。同样,硝苯地平和利尿剂的收缩压与舒张压平滑指数均相当高,表明两种药物的降压反应平衡程度相似。两个治疗组在心脑血管事件数量上未观察到显著差异(硝苯地平组17例,利尿剂组26例)。

结论

在INSIGHT研究中,硝苯地平对24小时血压的长期降压效果及心血管保护作用与利尿剂相似。

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