Jamerson Kenneth, Weber Michael A, Bakris George L, Dahlöf Björn, Pitt Bertram, Shi Victor, Hester Allen, Gupte Jitendra, Gatlin Marjorie, Velazquez Eric J
Division of Cardiovascular Medicine, University of Michigan Health System, 24 Frank Lloyd Wright Dr., Lobby M, Ann Arbor, MI 48106, USA.
N Engl J Med. 2008 Dec 4;359(23):2417-28. doi: 10.1056/NEJMoa0806182.
The optimal combination drug therapy for hypertension is not established, although current U.S. guidelines recommend inclusion of a diuretic. We hypothesized that treatment with the combination of an angiotensin-converting-enzyme (ACE) inhibitor and a dihydropyridine calcium-channel blocker would be more effective in reducing the rate of cardiovascular events than treatment with an ACE inhibitor plus a thiazide diuretic.
In a randomized, double-blind trial, we assigned 11,506 patients with hypertension who were at high risk for cardiovascular events to receive treatment with either benazepril plus amlodipine or benazepril plus hydrochlorothiazide. The primary end point was the composite of death from cardiovascular causes, nonfatal myocardial infarction, nonfatal stroke, hospitalization for angina, resuscitation after sudden cardiac arrest, and coronary revascularization.
The baseline characteristics of the two groups were similar. The trial was terminated early after a mean follow-up of 36 months, when the boundary of the prespecified stopping rule was exceeded. Mean blood pressures after dose adjustment were 131.6/73.3 mm Hg in the benazepril-amlodipine group and 132.5/74.4 mm Hg in the benazepril-hydrochlorothiazide group. There were 552 primary-outcome events in the benazepril-amlodipine group (9.6%) and 679 in the benazepril-hydrochlorothiazide group (11.8%), representing an absolute risk reduction with benazepril-amlodipine therapy of 2.2% and a relative risk reduction of 19.6% (hazard ratio, 0.80, 95% confidence interval [CI], 0.72 to 0.90; P<0.001). For the secondary end point of death from cardiovascular causes, nonfatal myocardial infarction, and nonfatal stroke, the hazard ratio was 0.79 (95% CI, 0.67 to 0.92; P=0.002). Rates of adverse events were consistent with those observed from clinical experience with the study drugs.
The benazepril-amlodipine combination was superior to the benazepril-hydrochlorothiazide combination in reducing cardiovascular events in patients with hypertension who were at high risk for such events. (ClinicalTrials.gov number, NCT00170950.)
尽管美国现行指南推荐使用利尿剂,但高血压的最佳联合药物治疗方案尚未确定。我们假设,与使用血管紧张素转换酶(ACE)抑制剂加噻嗪类利尿剂治疗相比,使用ACE抑制剂与二氢吡啶类钙通道阻滞剂联合治疗在降低心血管事件发生率方面更有效。
在一项随机、双盲试验中,我们将11506例有心血管事件高风险的高血压患者随机分组,分别接受贝那普利加氨氯地平或贝那普利加氢氯噻嗪治疗。主要终点是心血管原因死亡、非致死性心肌梗死、非致死性卒中、因心绞痛住院、心脏骤停复苏以及冠状动脉血运重建的复合终点。
两组的基线特征相似。在平均随访36个月后,当超过预先设定的停止规则界限时,试验提前终止。剂量调整后的平均血压在贝那普利 - 氨氯地平组为131.6/73.3 mmHg,在贝那普利 - 氢氯噻嗪组为132.5/74.4 mmHg。贝那普利 - 氨氯地平组有552例主要结局事件(9.6%),贝那普利 - 氢氯噻嗪组有679例(11.8%),这表明贝那普利 - 氨氯地平治疗的绝对风险降低了2.2%,相对风险降低了19.6%(风险比,0.80;95%置信区间[CI],0.72至0.90;P<0.001)。对于心血管原因死亡、非致死性心肌梗死和非致死性卒中的次要终点,风险比为0.79(95%CI,0.67至0.92;P = 0.002)。不良事件发生率与研究药物的临床经验观察结果一致。
在有心血管事件高风险的高血压患者中,贝那普利 - 氨氯地平联合用药在降低心血管事件方面优于贝那普利 - 氢氯噻嗪联合用药。(临床试验注册号,NCT00170950。)