Krittanawong Chayakrit, Maitra Neil Sagar, El-Sherbini Adham H, Shah Nishant, Lavie Carl J, Shapiro Michael D, Virani Salim S
Cardiology Division, NYU Langone Health and NYU School of Medicine, New York, NY, United States of America.
Division of Cardiology, Scripps Clinic, La Jolla, CA, United States of America.
Prog Cardiovasc Dis. 2023 Jul-Aug;79:28-36. doi: 10.1016/j.pcad.2023.07.006. Epub 2023 Jul 27.
Cardiovascular disease (CVD) remains the leading cause of death worldwide. Serum lipoprotein(a) (Lp(a)) has been shown to be an independent and causative risk factor for atherosclerotic CVD and calcific aortic valvular disease. Lp(a) continues to be studied, with emerging insights into the epidemiology of CVD with respect to Lp(a), pathogenic mechanisms of Lp(a) and strategies to mitigate disease. There have been novel insights into genetic polymorphisms of the LPA gene, interactions between concomitant risk factors and Lp(a) based on real-world data, and metabolic pathway targets for Lp(a) reduction. This review highlights these recent advances in our understanding of Lp(a) and discusses management strategies as recommended by cardiovascular professional societies, emerging therapies for lowering Lp(a), and future directions in targeting Lp(a) to reduce CVD.
心血管疾病(CVD)仍然是全球主要的死亡原因。血清脂蛋白(a)[Lp(a)]已被证明是动脉粥样硬化性心血管疾病和钙化性主动脉瓣疾病的独立致病危险因素。关于Lp(a)在心血管疾病流行病学方面、Lp(a)的致病机制以及减轻疾病的策略不断有新的见解,Lp(a)仍在持续研究中。对于LPA基因的遗传多态性、基于真实世界数据的伴随危险因素与Lp(a)之间的相互作用以及降低Lp(a)的代谢途径靶点都有了新的认识。本综述重点介绍了我们对Lp(a)认识的这些最新进展,并讨论了心血管专业学会推荐的管理策略、降低Lp(a)的新兴疗法以及靶向Lp(a)以减少心血管疾病的未来方向。