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极低剂量联合用药:高血压治疗的一线选择?

Very-low-dose combination: a first-line choice for the treatment of hypertension?

作者信息

Waeber Bernard

机构信息

Division of Clinical Pathophysiology, University Hospital, BH-19, 1011 Lausanne, Switzerland.

出版信息

J Hypertens Suppl. 2003 Jun;21(3):S3-10. doi: 10.1097/00004872-200306003-00002.

Abstract

Essential hypertension is a very heterogeneous disease and different pressor mechanisms might interact to increase blood pressure. It is therefore not surprising that antihypertensive drugs given as monotherapies normalize blood pressure in only a proportion of hypertensive patients. This is, for instance, the case for diuretics, angiotensin-converting enzyme (ACE) inhibitors and angiotensin II type 1 (AT1) receptor antagonists administered as single agents. The rationale for combining antihypertensive agents relates in part to the concept that the blood pressure-decreasing effect may be enhanced when two classes are coadministered. Also, combination treatment serves to counteract the counter-regulatory mechanisms that are triggered whenever pharmacologic intervention is initiated and act to limit the efficacy of the antihypertensive medication. For example, the compensatory increase in renin secretion induced by sodium depletion may become the predominant factor sustaining high blood pressure. Simultaneous blockade of the renin-angiotensin system, with either an ACE inhibitor or an AT1 receptor blocker, makes this compensatory hyper-reninaemia ineffective and allows maximum benefit from sodium depletion. The increased effectiveness obtained by combining a blocker of the renin-angiotensin system with a low dose of a diuretic is not obtained at the expense of reduced tolerability compared with the individual components administered alone. Fixed very-low-dose combinations containing an ACE inhibitor or an AT1 receptor blocker and a diuretic are therefore likely to become increasingly used, not only as second-line therapy, but also as first-line treatment. This is the case, for instance, for the fixed very-low-dose combination of the ACE inhibitor perindopril (2 mg) and the diuretic indapamide (0.625 mg), as this preparation is very effective in decreasing blood pressure while maintaining a tolerability that is similar to that of placebo.

摘要

原发性高血压是一种非常异质性的疾病,不同的升压机制可能相互作用以升高血压。因此,单一使用抗高血压药物仅能使一部分高血压患者的血压恢复正常也就不足为奇了。例如,利尿剂、血管紧张素转换酶(ACE)抑制剂和1型血管紧张素II(AT1)受体拮抗剂单独使用时就是这种情况。联合使用抗高血压药物的基本原理部分与这样一种概念相关,即当两类药物联合使用时,降压效果可能会增强。此外,联合治疗有助于抵消每当启动药物干预时就会触发的反调节机制,这些机制会限制抗高血压药物的疗效。例如,钠缺失引起的肾素分泌代偿性增加可能成为维持高血压的主要因素。同时使用ACE抑制剂或AT1受体阻滞剂阻断肾素-血管紧张素系统,可使这种代偿性高肾素血症无效,并使钠缺失获得最大益处。与单独使用各成分相比,联合使用肾素-血管紧张素系统阻滞剂和低剂量利尿剂所获得的增强疗效并非以降低耐受性为代价。因此,含有ACE抑制剂或AT1受体阻滞剂和利尿剂的固定极低剂量组合不仅可能越来越多地用作二线治疗,也可能用作一线治疗。例如,ACE抑制剂培哚普利(2毫克)和利尿剂吲达帕胺(0.625毫克)的固定极低剂量组合就是这种情况,因为这种制剂在降低血压方面非常有效,同时保持与安慰剂相似的耐受性。

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