Cardiology Department, Barzilai University Medical Center, Ben-Gurion University, Ashkelon, Israel.
Cardiology Department, Barzilai University Medical Center, Ben-Gurion University, Ashkelon, Israel.
Eur J Pharmacol. 2020 Jul 5;878:173114. doi: 10.1016/j.ejphar.2020.173114. Epub 2020 Apr 14.
The clinical benefit of lipid-lowering therapies is to reduce circulating levels of atherogenic particles and to ameliorate the risk of atherosclerotic cardiovascular disease (ASCVD). The completion of two major clinical trials on PCSK9 inhibitors (PCSK9i), the FOURIER and the ODYSSEY outcome trials, has marked the beginning of a new era of lipid-lowering drugs. PCSK9i, evolocumab and alirocumab, are monoclonal antibodies that inactivate the liver proprotein convertase subtilisin kexin 9 (PCSK9). Inhibition of PCSK9 increases the number of low-density lipoprotein (LDL) receptors available leading to a profound reduction in circulating LDL particles. By preventing LDL receptor destruction, PCSK9i as adjunct to statin therapy can reduce LDL-C by 50-60% above that achieved by statin therapy alone. In addition, PCSK9i in combination with high-dose statins may reduce cardiovascular events and all-cause mortality in patients with clinical ASCVD. Based on evidence from clinical trials, the 2019 European Society of Cardiology (ESC)/European Atherosclerosis Society (EAS) guidelines for the management of dyslipidemias now include the use of PCSK9i to very high-risk ASCVD patients who are not achieving treatment goals on a maximum tolerated dose of a statin and ezetimibe. However, the cost-effectiveness of PCSK9i therapy is limited to secondary prevention in high-risk patients. This review outlines the main clinical trials leading to a change in the guidelines, clinical practice as well as the future challenges of PCSK9i therapy.
降脂治疗的临床获益在于降低致动脉粥样硬化颗粒的循环水平,并改善动脉粥样硬化性心血管疾病(ASCVD)的风险。两项关于前蛋白转化酶枯草溶菌素 9(PCSK9)抑制剂(PCSK9i)的主要临床试验——FOURIER 和 ODYSSEY 结果试验的完成,标志着降脂药物新时代的开始。PCSK9i、依洛尤单抗和阿利西尤单抗是两种能够使肝前蛋白转化酶枯草溶菌素 9(PCSK9)失活的单克隆抗体。PCSK9 的抑制作用增加了可用的低密度脂蛋白(LDL)受体数量,从而导致循环 LDL 颗粒显著减少。通过防止 LDL 受体破坏,PCSK9i 与他汀类药物联合应用可使 LDL-C 降低 50%-60%,超过他汀类药物单独治疗的效果。此外,PCSK9i 联合高剂量他汀类药物可降低临床 ASCVD 患者的心血管事件和全因死亡率。基于临床试验证据,2019 年欧洲心脏病学会(ESC)/欧洲动脉粥样硬化学会(EAS)血脂异常管理指南现在包括使用 PCSK9i 治疗他汀类药物和依折麦布最大耐受剂量治疗未达标且存在极高 ASCVD 风险的患者。然而,PCSK9i 治疗的成本效益仅限于高危患者的二级预防。本综述概述了导致指南改变、临床实践以及 PCSK9i 治疗未来挑战的主要临床试验。