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血压降低而非血管作用机制是临床结局的主要决定因素。

Blood pressure lowering, not vascular mechanism of action, is the primary determinant of clinical outcome.

作者信息

Leenen Frans H H

机构信息

Hypertension Unit, University of Ottawa Heart Institute, Ottawa, Ontario.

出版信息

Can J Cardiol. 2004 Aug;20 Suppl B:77B-82B.

Abstract

A number of placebo-controlled randomized clinical trials have clearly established that blood pressure (BP) lowering, based on all antihypertensive drugs studied, lowers the risk of all major BP-related cardiovascular events. However, this does not exclude that some antihypertensive agents are more or less effective in preventing cardiovascular events than to be expected from the extent of BP lowering. Indeed, clinical trials of thiazide diuretics using 'high' doses demonstrated marked prevention of strokes, but little to no prevention of coronary events. Subsequent studies using thiazides at 'lower' doses showed prevention of both strokes and coronary events. Angiotensin converting enzyme inhibitors and calcium channel blockers exert direct vascular effects which may inhibit atherosclerosis and prevent cardiovascular events, in addition to their benefits related to BP lowering. After the publication of the results of Heart Outcome Prevention Evaluation (HOPE) trial, this concept has become widely accepted for angiotensin-converting enzyme inhibitors. However, placebo-controlled trials, such as HOPE and, recently, the European Trial on Reduction of Cardiac Events with Perindopril in Stable Coronary Artery Disease (EUROPA), are confounded by the difference in BP and its impact on outcome. Indeed, as a mirror image of these trials, the blacks subgroup in the Antihypertensive and Lipid-Lowering Treatment to Prevent Heart Attack Trial (ALLHAT) exhibited a 4 to 5 mmHg higher systolic BP on ACE inhibitor as compared with the diuretic, associated with 19% higher combined cardiovascular disease and 40% higher stroke rate. Recent overviews of randomized clinical trials comparing outcomes with different antihypertensive drug classes concluded that outcome benefits beyond BP lowering remain unproven.

摘要

多项安慰剂对照随机临床试验已明确证实,基于所有研究的抗高血压药物进行的血压降低,可降低所有主要血压相关心血管事件的风险。然而,这并不排除某些抗高血压药物在预防心血管事件方面或多或少比预期的血压降低效果更有效或更差。事实上,使用“高”剂量噻嗪类利尿剂的临床试验显示对中风有显著预防作用,但对冠状动脉事件几乎没有预防作用。随后使用“低”剂量噻嗪类药物的研究表明对中风和冠状动脉事件均有预防作用。除了与血压降低相关的益处外,血管紧张素转换酶抑制剂和钙通道阻滞剂还具有直接的血管作用,可能抑制动脉粥样硬化并预防心血管事件。在心脏结局预防评估(HOPE)试验结果发表后,这一概念已被广泛接受用于血管紧张素转换酶抑制剂。然而,安慰剂对照试验,如HOPE以及最近的欧洲稳定冠状动脉疾病培哚普利降低心脏事件试验(EUROPA),因血压差异及其对结局的影响而受到混淆。事实上,作为这些试验的镜像,抗高血压和降脂治疗预防心脏病发作试验(ALLHAT)中的黑人亚组与利尿剂相比,使用血管紧张素转换酶抑制剂时收缩压高4至5 mmHg,心血管疾病合并发生率高19%,中风率高40%。最近比较不同抗高血压药物类别结局的随机临床试验综述得出结论,除血压降低外的结局益处仍未得到证实。

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