Latimer James, Batty Jonathan A, Neely R Dermot G, Kunadian Vijay
Institute of Cellular Medicine, Faculty of Medical Sciences, Newcastle University, M3.131, 3rd Floor William Leech Building, Newcastle upon Tyne, NE2 4HH, UK.
Freeman Hospital, Newcastle upon Tyne NHS Foundation Trust, Newcastle upon Tyne, UK.
J Thromb Thrombolysis. 2016 Oct;42(3):405-19. doi: 10.1007/s11239-016-1364-1.
Reducing plasma levels of low-density lipoprotein cholesterol (LDL-C) remains the cornerstone in the primary and secondary prevention of cardiovascular disease. However, lack of efficacy and adverse effects mean that a substantial proportion of patients fail to achieve acceptable LDL-C levels with currently available lipid-lowering drugs. Over the last decade, inhibition of proprotein convertase subtilisin/kexin type 9 (PCSK9) has emerged as a promising therapeutic strategy to reduce residual cardiovascular disease risk. Binding of PCSK9 to the LDL receptor targets the receptor for lysosomal degradation. The recognition that inhibition of PCSK9 increases LDL receptor activity has led to the development of a number of approaches to directly target PCSK9. Numerous monoclonal antibodies against PCSK9 are currently being evaluated in phase 3 trials, involving various patient categories on different background lipid-lowering therapies. Current evidence shows reductions in LDL-C levels of up to 70 % may be achieved with PCSK9 inhibition, independent of background statin therapy. This review examines the most recent evidence and future prospects for the use of PCSK9 inhibitors in the prevention of cardiovascular disease.
降低血浆低密度脂蛋白胆固醇(LDL-C)水平仍然是心血管疾病一级和二级预防的基石。然而,现有降脂药物缺乏疗效且存在不良反应,这意味着相当一部分患者无法通过目前可用的药物将LDL-C水平降至可接受范围。在过去十年中,抑制前蛋白转化酶枯草溶菌素9型(PCSK9)已成为降低残余心血管疾病风险的一种有前景的治疗策略。PCSK9与低密度脂蛋白受体结合后,会将该受体靶向溶酶体进行降解。认识到抑制PCSK9可增加低密度脂蛋白受体活性后,人们开发了多种直接靶向PCSK9的方法。目前,许多针对PCSK9的单克隆抗体正在3期试验中进行评估,涉及接受不同背景降脂治疗的各类患者。目前的证据表明,抑制PCSK9可使LDL-C水平降低达70%,且与背景他汀类药物治疗无关。本文综述了使用PCSK9抑制剂预防心血管疾病的最新证据和未来前景。