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体型和降压治疗对心血管事件发生率的影响:ACCOMPLISH 随机对照试验的亚组分析。

Effects of body size and hypertension treatments on cardiovascular event rates: subanalysis of the ACCOMPLISH randomised controlled trial.

机构信息

State University of New York, Downstate College of Medicine, Brooklyn, NY 11203, USA.

出版信息

Lancet. 2013 Feb 16;381(9866):537-45. doi: 10.1016/S0140-6736(12)61343-9. Epub 2012 Dec 6.

Abstract

BACKGROUND

In previous clinical trials in high-risk hypertensive patients, paradoxically higher cardiovascular event rates have been reported in patients of normal weight compared with obese individuals. As a prespecified analysis of the Avoiding Cardiovascular Events through Combination Therapy in Patients Living with Systolic Hypertension (ACCOMPLISH) trial, we aimed to investigate whether the type of hypertension treatment affects patients' cardiovascular outcomes according to their body size.

METHODS

On the basis of body-mass index (BMI), we divided the full ACCOMPLISH cohort into obese (BMI ≥30, n=5709), overweight (≥25 to <30, n=4157), or normal weight (<25, n=1616) categories. The ACCOMPLISH cohort had already been randomised to treatment with single-pill combinations of either benazepril and hydrochlorothiazide or benazepril and amlodipine. We compared event rates (adjusted for age, sex, diabetes, previous cardiovascular events, stroke, or chronic kidney disease) for the primary endpoint of cardiovascular death or non-fatal myocardial infarction or stroke. The analysis was by intention to treat. This trial is registered with ClinicalTrials.gov, number NCT00170950.

FINDINGS

In patients allocated benazepril and hydrochlorothiazide, the primary endpoint (per 1000 patient-years) was 30·7 in normal weight, 21·9 in overweight, and 18·2 in obese patients (overall p=0·0034). However, in those allocated benazepril and amlodipine, the primary endpoint did not differ between the three BMI groups (18·2, 16·9, and 16·5, respectively; overall p=0·9721). In obese individuals, primary event rates were similar with both benazepril and hydrochlorothiazide and benazepril and amlodipine, but rates were significantly lower with benazepril and amlodipine in overweight patients (hazard ratio 0·76, 95% CI 0·59-0·94; p=0·0369) and those of normal weight (0·57, 0·39-0·84; p=0·0037).

INTERPRETATION

Hypertension in normal weight and obese patients might be mediated by different mechanisms. Thiazide-based treatment gives less cardiovascular protection in normal weight than obese patients, but amlodipine-based therapy is equally effective across BMI subgroups and thus offers superior cardiovascular protection in non-obese hypertension.

FUNDING

Novartis Pharmaceuticals.

摘要

背景

在先前针对高危高血压患者的临床试验中,与肥胖个体相比,体重正常的患者报告的心血管事件发生率更高,这令人感到矛盾。作为避免心血管事件的组合治疗在患有收缩期高血压的患者中(ACCOMPLISH)试验的预先指定分析,我们旨在研究根据患者的体型,高血压治疗类型是否会影响患者的心血管结局。

方法

根据体重指数(BMI),我们将完整的 ACCOMPLISH 队列分为肥胖(BMI≥30,n=5709)、超重(≥25 至<30,n=4157)或正常体重(<25,n=1616)类别。ACCOMPLISH 队列已经被随机分配接受单一药丸组合的贝那普利和氢氯噻嗪或贝那普利和氨氯地平治疗。我们比较了主要终点(心血管死亡或非致死性心肌梗死或中风的调整年龄、性别、糖尿病、先前的心血管事件、中风或慢性肾病)的事件发生率。分析采用意向治疗。这项试验在 ClinicalTrials.gov 注册,编号为 NCT00170950。

结果

在接受贝那普利和氢氯噻嗪治疗的患者中,主要终点(每 1000 患者年)在正常体重组为 30.7,超重组为 21.9,肥胖组为 18.2(总体 p=0.0034)。然而,在接受贝那普利和氨氯地平治疗的患者中,三个 BMI 组之间的主要终点没有差异(分别为 18.2、16.9 和 16.5;总体 p=0.9721)。在肥胖患者中,贝那普利和氢氯噻嗪与贝那普利和氨氯地平的主要事件发生率相似,但在超重患者(风险比 0.76,95%CI 0.59-0.94;p=0.0369)和正常体重患者(0.57,0.39-0.84;p=0.0037)中,贝那普利和氨氯地平的治疗率显著较低。

解释

正常体重和肥胖患者的高血压可能由不同的机制介导。基于噻嗪类药物的治疗在正常体重患者中的心血管保护作用不如肥胖患者,而基于氨氯地平的治疗在所有 BMI 亚组中均同样有效,因此在非肥胖高血压患者中提供了更好的心血管保护作用。

资金来源

诺华制药公司。

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