Izzo Joseph L, Moser Marvin
Department of Medicine, State University of New York at Buffalo, Buffalo, NY 14209, USA.
J Clin Hypertens (Greenwich). 2002 Nov-Dec;4(6 Suppl 2):11-9, 31. doi: 10.1111/j.1524-6175.2002.01361.x.
Clinical trials have proved that blockade of the renin-angiotensin-aldosterone system (RAAS) offers primary and secondary protection of the cardiovascular system, brain, and kidneys. Drugs that interrupt the RAAS do so by several diverse mechanisms but it remains to be fully proved whether these mechanistic differences are associated with meaningful differences in clinical outcomes. This review summarizes current information about the basic mechanisms of action of three classes of anti-RAAS drugs: angiotensin-converting enzyme (ACE) inhibitors, combined ACE-neutral endopeptidase inhibitors, and angiotensin receptor antagonists as well as results of major clinical outcome trials with these agents. Basic and clinical science information is then blended with insights from the clinical pharmacology of anti-RAAS drugs to address four current controversies in clinical medicine: whether ACE inhibitors and angiotensin receptor antagonists are interchangeable, optimal dosing of available agents, potential justification of ACE inhibitor/angiotensin receptor antagonist combinations, and first-line use of anti-RAAS drugs in antihypertensive therapy.
临床试验已证明,阻断肾素-血管紧张素-醛固酮系统(RAAS)可为心血管系统、大脑和肾脏提供一级和二级保护。阻断RAAS的药物通过多种不同机制发挥作用,但这些机制差异是否与临床结局的显著差异相关仍有待充分证实。本综述总结了三类抗RAAS药物(血管紧张素转换酶(ACE)抑制剂、ACE-中性内肽酶联合抑制剂和血管紧张素受体拮抗剂)的基本作用机制的现有信息,以及使用这些药物的主要临床结局试验结果。然后,将基础和临床科学信息与抗RAAS药物临床药理学的见解相结合,以解决临床医学中当前的四个争议问题:ACE抑制剂和血管紧张素受体拮抗剂是否可互换、现有药物的最佳剂量、ACE抑制剂/血管紧张素受体拮抗剂联合使用的潜在合理性,以及抗RAAS药物在抗高血压治疗中的一线使用。