Ito Matthew K, Santos Raul D
Sanofi US, Bridgewater, NJ, USA.
Oregon State University/Oregon Health and Science University, College of Pharmacy, Portland, OR, USA (during initial development of this article).
J Clin Pharmacol. 2017 Jan;57(1):7-32. doi: 10.1002/jcph.766. Epub 2016 Jun 21.
Current guidelines for hypercholesterolemia treatment emphasize lifestyle modification and lipid-modifying therapy to reduce the risk for cardiovascular disease. Statins are the primary class of agents used for the treatment of hypercholesterolemia. Although statins are effective for many patients, they fail to achieve optimal reduction in lipids for some patients, including those who have or are at high risk for cardiovascular disease. The PCSK9 gene was identified in the past decade as a potential therapeutic target for the management of patients with hypercholesterolemia. Pharmacologic interventions to decrease PCSK9 levels are in development, with the most promising approach using monoclonal antibodies that bind to PCSK9 in the plasma. Two monoclonal antibodies, alirocumab and evolocumab, have recently been approved for the treatment of hypercholesterolemia, and a third one, bococizumab, is in phase 3 clinical development. All 3 agents achieve significant reductions in levels of low-density lipoprotein cholesterol, as well as reductions in non-high-density lipoprotein cholesterol, apolipoprotein B, and lipoprotein(a). Long-term outcome trials are under way to determine the sustained efficacy, safety, and tolerability of PCSK9 inhibitors and whether this novel class of agents decreases the risk for major cardiovascular events in patients on lipid-modifying therapy. Available data suggest that PCSK9 inhibitors provide a robust reduction in atherogenic cholesterol levels with a good safety profile, especially for patients who fail to obtain an optimal clinical response to statin therapy, those who are statin intolerant or have contraindications to statin therapy, and those with familial hypercholesterolemia.
当前的高胆固醇血症治疗指南强调生活方式的改变和脂质调节治疗,以降低心血管疾病的风险。他汀类药物是用于治疗高胆固醇血症的主要药物类别。尽管他汀类药物对许多患者有效,但对于一些患者,包括那些患有心血管疾病或有心血管疾病高风险的患者,它们未能实现脂质的最佳降低。在过去十年中,PCSK9基因被确定为高胆固醇血症患者管理的潜在治疗靶点。降低PCSK9水平的药物干预正在研发中,最有前景的方法是使用与血浆中的PCSK9结合的单克隆抗体。两种单克隆抗体,阿利西尤单抗和依洛尤单抗,最近已被批准用于治疗高胆固醇血症,第三种,博科西单抗,正处于3期临床开发阶段。所有这三种药物都能显著降低低密度脂蛋白胆固醇水平,以及降低非高密度脂蛋白胆固醇、载脂蛋白B和脂蛋白(a)。正在进行长期结局试验,以确定PCSK9抑制剂的持续疗效、安全性和耐受性,以及这类新型药物是否能降低接受脂质调节治疗的患者发生主要心血管事件的风险。现有数据表明,PCSK9抑制剂能显著降低致动脉粥样硬化胆固醇水平,且安全性良好,特别是对于那些对他汀类治疗未能获得最佳临床反应的患者、他汀类不耐受或有他汀类治疗禁忌证的患者,以及家族性高胆固醇血症患者。