Omari Muntaser, Alkhalil Mohammad
Cardiothoracic Centre, Freeman Hospital, Newcastle-upon-Tyne NE7 7DN, UK.
Translational and Clinical Research Institute, Newcastle University, Newcastle-upon-Tyne NE1 7RU, UK.
J Cardiovasc Dev Dis. 2024 Apr 21;11(4):126. doi: 10.3390/jcdd11040126.
Patients with atherosclerotic disease remain at increased risk of future events despite receiving optimal medical treatment. This residual risk is widely heterogeneous, but lipoprotein particles and their content play a major role in determining future cardiovascular events. Beyond low-density lipoprotein cholesterol (LDL-c), other lipoprotein particles have not demonstrated similar contribution to the progression of atherosclerosis. Statins, ezetimibe, and more recently, proprotein convertase subtilisin kexin 9 (PCSK9) inhibitors and bempedoic acid have confirmed the causal role of LDL-c in the development of atherosclerosis. Data on high-density lipoprotein cholesterol (HDL-c) suggested a possible causal role for atherosclerosis; nonetheless, HDL-c-raising treatments, including cholesteryl-ester transfer protein (CETP) inhibitors and niacin, failed to confirm this relationship. On the other hand, mendelian randomisation revealed that triglycerides are more implicated in the development of atherosclerosis. Although the use of highly purified eicosapentaenoic acid (EPA) was associated with a reduction in the risk of adverse cardiovascular events, this beneficial effect did not correlate with the reduction in triglycerides level and has not been consistent across large phase 3 trials. Moreover, other triglyceride-lowering treatments, such as fibrates, were not associated with a reduction in future cardiovascular risk. Studies assessing agents targeting angiopoietin-like 3 (lipoprotein lipase inhibitor) and apolipoprotein C3 antisense will add further insights into the role of triglycerides in atherosclerosis. Emerging lipid markers such as lipoprotein (a) and cholesterol efflux capacity may have a direct role in the progression of atherosclerosis. Targeting these biomarkers may provide incremental benefits in reducing cardiovascular risk when added to optimal medical treatment. This Review aims to assess available therapies for current lipid biomarkers and provide mechanistic insight into their potential role in reducing future cardiovascular risk.
尽管接受了最佳药物治疗,但动脉粥样硬化疾病患者未来发生事件的风险仍然增加。这种残余风险差异很大,但脂蛋白颗粒及其成分在决定未来心血管事件方面起着主要作用。除了低密度脂蛋白胆固醇(LDL-c)外,其他脂蛋白颗粒对动脉粥样硬化进展的作用尚未得到类似证实。他汀类药物、依折麦布,以及最近的前蛋白转化酶枯草溶菌素9(PCSK9)抑制剂和贝派地酸,均证实了LDL-c在动脉粥样硬化发展中的因果作用。关于高密度脂蛋白胆固醇(HDL-c)的数据表明其可能在动脉粥样硬化中起因果作用;尽管如此,包括胆固醇酯转移蛋白(CETP)抑制剂和烟酸在内的升高HDL-c的治疗方法,并未证实这种关系。另一方面,孟德尔随机化研究表明,甘油三酯与动脉粥样硬化的发展关系更为密切。虽然使用高度纯化的二十碳五烯酸(EPA)与不良心血管事件风险降低有关,但这种有益效果与甘油三酯水平降低并无关联,且在大型3期试验中也不一致。此外,其他降低甘油三酯的治疗方法,如贝特类药物,与未来心血管风险降低无关。评估靶向血管生成素样3(脂蛋白脂肪酶抑制剂)和载脂蛋白C3反义寡核苷酸药物的研究,将进一步深入了解甘油三酯在动脉粥样硬化中的作用。新兴的脂质生物标志物,如脂蛋白(a)和胆固醇流出能力,可能在动脉粥样硬化进展中直接发挥作用。在最佳药物治疗基础上,针对这些生物标志物可能会在降低心血管风险方面带来额外益处。本综述旨在评估针对当前脂质生物标志物的现有疗法,并深入探讨其在降低未来心血管风险方面的潜在作用机制。