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Statins and PCSK9 inhibitors: A new lipid-lowering therapy

机译:他汀类药物和PCSK9抑制剂:一种新的脂质降低治疗

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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.
机译:降脂治疗的临床益处是降低动脉粥样硬化的颗粒的循环水平和改善动脉粥样硬化心血管病(ASCVD)的风险。对PCSK9抑制剂两大临床试验(PCSK9i),傅立叶和奥德赛结局试验,建成,标志着降脂药物的新时代的开始。 PCSK9i,evolocumab和alirocumab,是失活肝前蛋白转化酶枯草杆菌蛋白酶Kexin 9(PCSK9)的单克隆抗体。 PCSK9的抑制增加的低密度脂蛋白(LDL)的数量受体可用导致循环的LDL颗粒的深刻减少。通过防止LDL受体的破坏,如PCSK9i辅助他汀类药物可以由50-60%降低LDL-C以上,通过单独他汀治疗来实现。此外,在PCSK9i高剂量他汀类组合可以降低心血管事件和患者的全因死亡率与临床ASCVD。基于临床试验的证据,2019年欧洲心脏病学会(ESC)/欧洲动脉硬化学会(EAS),血脂异常的管理方针,现在包括使用PCSK9i来谁不是在达到治疗目标非常高风险的ASCVD患者最大耐受他汀类药物和依泽替米贝的剂量。然而,PCSK9i治疗的成本效益仅限于二级预防的高危患者。本次审查概述了主要的临床试验导致的准则的改变,临床实践以及PCSK9i治疗的未来的挑战。

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