Meredith Peter A
Department of Medicine and Therapeutics, University of Glasgow, Western Infirmary, Glasgow, UK.
Curr Med Res Opin. 2007 Jul;23(7):1693-705. doi: 10.1185/030079907x210723.
Therapeutic interventions that block the renin-angiotensin-aldosterone system (RAAS) have an important role in slowing the progression of cardiovascular risk actors to established cardiovascular diseases. In recent years, angiotensin receptor blockers (ARBs) have emerged as effective and well-tolerated alternatives to an angiotensin-converting enzyme inhibitor (ACEi) for RAAS blockade. The ARB candesartan was initially established as an effective once-daily antihypertensive treatment, providing 24-h blood pressure (BP) control with a trough:peak ratio close to 100%.
A Medline literature search was undertaken to identify randomised, controlled trials that examined the efficacy and cardiovascular outcomes associated with candesartan cilexetil in hypertension and chronic heart failure (CHF).
Compared with other ARBs, candesartan demonstrates the strongest binding affinity to the angiotensin II type 1 receptor. Clinical trials have demonstrated that candesartan is well tolerated in combination with diuretics or calcium channel blockers (CCBs), making it a suitable treatment option for patients whose hypertension is not adequately controlled by monotherapy. Subsequently, candesartan became the only ARB licensed in the UK to treat patients with CHF and left ventricular ejection fraction < or = 40% as add-on therapy to an ACEi or when an ACEi is not tolerated. Studies in patients with symptomatic HF have indicated that candesartan treatment was associated with significant relative risk reductions in cardiovascular mortality and hospitalisation due to CHF.
There are clear indications that the clinical benefits of candesartan may extend beyond its proven antihypertensive effects to a wider range of complications across the cardiovascular continuum, including diabetes, left ventricular hypertrophy, atherosclerosis and stroke. Such results suggest that candesartan treatment may offer significant patient benefits as well as practical advantages over conventional treatment.
阻断肾素 - 血管紧张素 - 醛固酮系统(RAAS)的治疗干预措施在减缓心血管危险因素发展为既定心血管疾病的进程中发挥着重要作用。近年来,血管紧张素受体阻滞剂(ARB)已成为用于RAAS阻断的血管紧张素转换酶抑制剂(ACEi)的有效且耐受性良好的替代药物。ARB坎地沙坦最初被确立为一种有效的每日一次抗高血压治疗药物,能实现24小时血压(BP)控制,谷峰比值接近100%。
进行了一项Medline文献检索,以确定研究坎地沙坦酯在高血压和慢性心力衰竭(CHF)中的疗效及心血管结局的随机对照试验。
与其他ARB相比,坎地沙坦对血管紧张素II 1型受体表现出最强的结合亲和力。临床试验表明,坎地沙坦与利尿剂或钙通道阻滞剂(CCB)联合使用时耐受性良好,使其成为单药治疗不能充分控制高血压患者的合适治疗选择。随后,坎地沙坦成为英国唯一获批用于治疗CHF且左心室射血分数≤40%的患者的ARB,可作为ACEi的附加治疗或在不能耐受ACEi时使用。对有症状HF患者的研究表明,坎地沙坦治疗与心血管死亡率和因CHF住院的相对风险显著降低相关。
有明确迹象表明,坎地沙坦的临床益处可能超出其已证实的抗高血压作用,延伸至心血管连续体的更广泛并发症,包括糖尿病、左心室肥厚、动脉粥样硬化和中风。这些结果表明,坎地沙坦治疗可能为患者带来显著益处,且相对于传统治疗具有实际优势。