Billecke Scott S, Marcovitz P A
William Beaumont Hospital, Ministrelli Women's Heart Center, Royal Oak, Michigan 48073, USA.
Drugs Today (Barc). 2011 Jun;47(6):403-17. doi: 10.1358/dot.2011.47.6.1603505.
The challenge of managing hypertension is exemplified by the limited success of monotherapy and necessity for multiple drug regimens targeting complimentary pathways. Recent evidence suggests that combination therapy including angiotensin-converting enzyme (ACE) inhibitors and calcium channel blockers (CCBs) provides blood pressure control while reducing cardiovascular mortality and morbidity over ACE inhibitor/diuretic therapy. However, CCBs, ACE inhibitors and angiotensin receptor blockers all increase plasma renin activity (PRA), promoting angiotensin I accumulation and angiotensin II production through alternative pathways. While the clinical ramifications of this and other compensatory pathways activating the renin-angiotensin-aldosterone system are unclear, the recently approved aliskiren/amlodipine antihypertensive combination pill has been shown to decrease PRA via aliskiren's direct inhibition of renin. The purpose of this monograph is to review the mechanisms of action, pharmacodynamics, and safety and efficacy profile of the aliskiren/amlodipine combination pill.
单药治疗效果有限,且需要针对互补途径采用多种药物治疗方案,这体现了高血压管理面临的挑战。最近的证据表明,与血管紧张素转换酶抑制剂/利尿剂疗法相比,包括血管紧张素转换酶(ACE)抑制剂和钙通道阻滞剂(CCB)的联合疗法在控制血压的同时,还能降低心血管疾病的死亡率和发病率。然而,CCB、ACE抑制剂和血管紧张素受体阻滞剂都会增加血浆肾素活性(PRA),通过替代途径促进血管紧张素I的积累和血管紧张素II的产生。虽然这种及其他激活肾素-血管紧张素-醛固酮系统的代偿途径的临床影响尚不清楚,但最近获批的阿利吉仑/氨氯地平降压复方药丸已被证明可通过阿利吉仑对肾素的直接抑制作用降低PRA。本专著的目的是综述阿利吉仑/氨氯地平复方药丸的作用机制、药效学以及安全性和有效性。