动脉粥样硬化残余血脂风险--现有和未来药物疗法概述。

Muntaser Omari, M. Alkhalil
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引用次数: 0

摘要

患有动脉粥样硬化疾病的患者尽管接受了最佳治疗,但未来发生心血管事件的风险仍然会增加。这种残余风险具有广泛的异质性,但脂蛋白颗粒及其含量在决定未来心血管事件中起着重要作用。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的发展也没有类似的作用。他汀类药物、依折麦布以及最近的丙蛋白转换酶枯草蛋白酶 9(PCSK9)抑制剂和贝母多酸证实了低密度脂蛋白胆固醇在动脉粥样硬化发展过程中的因果作用。有关高密度脂蛋白胆固醇(HDL-c)的数据表明,高密度脂蛋白胆固醇在动脉粥样硬化中可能起着因果作用;然而,包括胆固醇酯转移蛋白(CETP)抑制剂和烟酸在内的提高高密度脂蛋白胆固醇的治疗方法未能证实这种关系。另一方面,"泯灭随机法 "显示,甘油三酯与动脉粥样硬化的发生有更大的关系。虽然使用高纯度二十碳五烯酸(EPA)与降低不良心血管事件的风险有关,但这种有益效果与甘油三酯水平的降低并不相关,在大型三期试验中也不一致。此外,其他降低甘油三酯的疗法,如纤维酸盐,也与降低未来心血管风险无关。评估以血管生成素样 3(脂蛋白脂酶抑制剂)和载脂蛋白 C3 反义为靶点的药物的研究将进一步揭示甘油三酯在动脉粥样硬化中的作用。脂蛋白(a)和胆固醇外流能力等新出现的脂质标志物可能在动脉粥样硬化的进展中起着直接作用。在最佳治疗的基础上,针对这些生物标志物进行治疗可能会在降低心血管风险方面带来更多益处。本综述旨在评估针对当前血脂生物标志物的现有疗法,并从机理上深入探讨这些疗法在降低未来心血管风险方面的潜在作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Atherosclerosis Residual Lipid Risk-Overview of Existing and Future Pharmacotherapies.
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.
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