Kim Kyung An, Park Hun-Jun
Division of Cardiology, Department of Internal Medicine, Seoul St. Mary's Hospital, The Catholic University of Korea, Seoul, Korea.
J Lipid Atheroscler. 2023 Jan;12(1):37-46. doi: 10.12997/jla.2023.12.1.37. Epub 2022 Nov 17.
Dyslipidemia is an important risk factor for atherosclerotic cardiovascular disease (ASCVD). There are abundant and unequivocal data to indicate that low-density lipoproteins (LDL) are a cause of ASCVD. Reduction of plasma low-density lipoprotein cholesterol (LDL-C) by medical therapy such as statins, ezetimibe and proprotein convertase subtilisin/kexin type 9 (PCSK9) inhibitors have proven to significantly reduce the risk of cardiovascular events. However, for many reasons, many patients are not able to achieve LDL-C levels recommended by guidelines on currently available therapies. This has led to the development of new drugs lowering LDL-C, such as inclisiran, bempedoic acid, and evinacumab, in the hope of reducing cardiovascular (CV) risk. Drugs targeting lipoprotein (a) (Lp[a]) also have a role in the prevention of atherosclerosis, with genetic studies having established that 20%-30% of the human population inherits plasma Lp(a) levels in the atherogenic range. In this paper, we will review the recent progress made in the approaches to LDL-C and Lp(a) therapeutic modulation.
血脂异常是动脉粥样硬化性心血管疾病(ASCVD)的重要危险因素。有大量明确的数据表明,低密度脂蛋白(LDL)是ASCVD的一个病因。通过他汀类药物、依折麦布和前蛋白转化酶枯草溶菌素/ kexin 9型(PCSK9)抑制剂等药物治疗降低血浆低密度脂蛋白胆固醇(LDL-C)已被证明可显著降低心血管事件风险。然而,由于多种原因,许多患者无法通过目前可用的治疗方法达到指南推荐的LDL-C水平。这促使了新型降低LDL-C药物的研发,如英克西兰、贝派地酸和依维那单抗,以期降低心血管(CV)风险。靶向脂蛋白(a)[Lp(a)]的药物在动脉粥样硬化预防中也发挥着作用,基因研究表明,20% - 30%的人群遗传了处于致动脉粥样硬化范围内的血浆Lp(a)水平。在本文中,我们将综述LDL-C和Lp(a)治疗调控方法的最新进展。