Munger Mark A
Dr. Munger is Professor of Pharmacotherapy and Internal Medicine and Associate Dean of Academic Affairs at the College of Pharmacy of the University of Utah in Salt Lake City, Utah.
P T. 2011 Jan;36(1):22-40.
To differentiate angiotensin II receptor blockers (ARBs) by vascular effects and outcomes in trials on cardio-protective endpoints.
MEDLINE searches were conducted from January 2003 to March 2009 using the following search terms: renin-angiotensin-aldosterone system (RAAS) blockade or inhibition; angiotensin II receptor blocker (ARBs); cardio-protection; vascular protection; end-organ protection; candesartan; eprosartan, irbesartan; losartan; olmesartan; telmisartan; and valsartan. Ongoing and recruiting clinical trials were identified via Clinicaltrials.gov (July 2008).
Pertinent basic science research and clinical trials with cardiovascular endpoints and information from reviews, American Heart Association 2009 statistics, and The Seventh Report of the Joint National Committee on Prevention, Detection, Evaluation, and Treatment of High Blood Pressure guidelines were included in this review.
ARBs differ in their vascular protective pleiotropic effects and pharmacokinetic properties, which may contribute to their pharmacological protection to reduce cardiovascular morbidity and mortality, independently of their blood pressure (BP)-lowering effects.
Emerging data show that ARBs are effective in hypertension, left ventricular hypertrophy, postmyocardial infarction, and heart failure. To what extent their pleiotropic effects, independent of BP lowering, contribute to these outcomes will be the focus of research in the coming years. Well-designed, comparative-effectiveness studies are needed to clinically differentiate this class of agents. The future will be marked by multifunctional ARBs that will pharmacologically do more than antagonize the angiotensin type I (AT(1)) receptor.
在心脏保护终点试验中,根据血管效应和结果区分血管紧张素II受体阻滞剂(ARB)。
2003年1月至2009年3月期间,使用以下检索词在MEDLINE数据库进行检索:肾素-血管紧张素-醛固酮系统(RAAS)阻断或抑制;血管紧张素II受体阻滞剂(ARB);心脏保护;血管保护;靶器官保护;坎地沙坦;依普罗沙坦;厄贝沙坦;氯沙坦;奥美沙坦;替米沙坦;缬沙坦。通过Clinicaltrials.gov(2008年7月)确定正在进行和招募患者的临床试验。
本综述纳入了相关的基础科学研究、具有心血管终点的临床试验以及来自综述、美国心脏协会2009年统计数据和美国预防、检测、评估与治疗高血压联合委员会第七次报告指南的信息。
ARB在其血管保护的多效性作用和药代动力学特性方面存在差异,这可能有助于它们在降低血压(BP)作用之外,通过药理保护作用降低心血管发病率和死亡率。
新出现的数据表明,ARB在高血压、左心室肥厚、心肌梗死后和心力衰竭方面有效。在未来几年,它们的多效性作用(独立于血压降低)在多大程度上促成这些结果将成为研究重点。需要设计良好的比较有效性研究,以便在临床上区分这类药物。未来的特点将是多功能ARB,其药理作用将不仅仅是拮抗血管紧张素I型(AT(1))受体。