Lam Sum, Choy Mary
Department of Clinical Pharmacy Practice, College of Pharmacy and Allied Health Professions, St. John's University, Jamaica, New York 11439, USA.
Cardiol Rev. 2007 Nov-Dec;15(6):316-23. doi: 10.1097/CRD.0b013e31814852a4.
Hypertension is a common chronic disease that leads to significant cardiovascular morbidity and mortality worldwide. Blood pressure control is critical in reducing the end-organ complications, such as stroke, myocardial infarction, heart failure, or kidney disease. Currently available antihypertensive agents work by different mechanisms to reduce blood pressure. Aliskiren, a novel direct renin inhibitor, lowers blood pressure by decreasing renin activity, and angiotensin I and II levels. At the approved dosage (150-300 mg once daily), it reduces systolic blood pressure by 12-16 mm Hg and diastolic blood pressure by 2-12 mm Hg. In studies its efficacy was comparable to losartan 100 mg, irbesartan 150 mg, and valsartan 80-320 mg. When used adjunctively with ramipril, an angiotensin-converting enzyme (ACE) inhibitor, valsartan, an angiotensin II receptor blocker (ARB), or hydrochlorothiazide, a diuretic, it provides additional blood pressure reduction compared with placebo or monotherapy. Aliskiren is well tolerated, with the most common side effects being gastrointestinal symptoms, fatigue, weakness, and headache. In short-term clinical trials, aliskiren caused fewer disturbances in potassium levels when compared with hydrochlorothiazide, ACE inhibitors and ARBs. Long-term data on morbidity and mortality outcomes are not currently available, thus it is unknown whether aliskiren would join ACE inhibitors and ARBs as the preferred hypertensive agents for end organ protection. At this time, aliskiren should be considered as an alternative agent for mild-to-moderate hypertension, or as an adjunctive therapy when preferred agents fail to maintain optimal blood pressure control. It is also an option for those patients who have contraindications or intolerability to other antihypertensive agents, including dry cough induced by ACE inhibitors.
高血压是一种常见的慢性疾病,在全球范围内导致显著的心血管发病率和死亡率。血压控制对于减少诸如中风、心肌梗死、心力衰竭或肾脏疾病等靶器官并发症至关重要。目前可用的抗高血压药物通过不同机制降低血压。阿利吉仑是一种新型直接肾素抑制剂,通过降低肾素活性以及血管紧张素I和II水平来降低血压。在批准剂量(每日一次150 - 300毫克)下,它可使收缩压降低12 - 16毫米汞柱,舒张压降低2 - 12毫米汞柱。在研究中,其疗效与100毫克氯沙坦、150毫克厄贝沙坦和80 - 320毫克缬沙坦相当。当与血管紧张素转换酶(ACE)抑制剂雷米普利、血管紧张素II受体阻滞剂(ARB)缬沙坦或利尿剂氢氯噻嗪联合使用时,与安慰剂或单一疗法相比,它能进一步降低血压。阿利吉仑耐受性良好,最常见的副作用是胃肠道症状、疲劳、虚弱和头痛。在短期临床试验中,与氢氯噻嗪、ACE抑制剂和ARB相比,阿利吉仑引起的钾水平紊乱较少。目前尚无关于发病率和死亡率结局的长期数据,因此尚不清楚阿利吉仑是否会与ACE抑制剂和ARB一样成为用于靶器官保护的首选高血压药物。此时,阿利吉仑应被视为轻度至中度高血压的替代药物,或在首选药物未能维持最佳血压控制时作为辅助治疗。对于那些对其他抗高血压药物有禁忌或不耐受的患者,包括ACE抑制剂引起的干咳,它也是一种选择。