Lu Yongzheng, Cui Xiaolin, Zhang Li, Wang Xu, Xu Yanyan, Qin Zhen, Liu Gangqiong, Wang Qiguang, Tian Kang, Lim Khoon S, Charles Chris J, Zhang Jinying, Tang Junnan
1Department of Cardiology, the First Affiliated Hospital of Zhengzhou University, Zhengzhou, Henan, China.
2Key Laboratory of Cardiac Injury and Repair of Henan Province, Zhengzhou, Henan, China.
Aging Dis. 2022 Apr 1;13(2):491-520. doi: 10.14336/AD.2021.0929. eCollection 2022 Apr.
Dyslipidemia, characterized by a high level of lipids (cholesterol, triglycerides, or both), can increase the risk of developing and progressing atherosclerosis. As atherosclerosis progresses, the number and severity of aterial plagues increases with greater risk of myocardial infarction, a major contributor to cardiovascular mortality. Atherosclerosis progresses in four phases, namely endothelial dysfunction, fatty streak formation, lesion progression and plaque rupture, and eventually thrombosis and arterial obstruction. With greater understanding of the pathological processes underlying atherosclerosis, researchers have identified that lipoproteins play a significant role in the development of atherosclerosis. In particular, apolipoprotein B (apoB)-containing lipoproteins have been shown to associate with atherosclerosis. Oxidized low-density lipoproteins (ox-LDLs) also contribute to the progression of atherosclerosis whereas high-density lipoproteins (HDL) contribute to the removal of cholesterol from macrophages thereby inhibiting the formation of foam cells. Given these known associations, lipoproteins may have potential as biomarkers for predicting risk associated with atherosclerotic plaques or may be targets as novel therapeutic agents. As such, the rapid development of drugs targeting lipoprotein metabolism may lead to novel treatments for atherosclerosis. A comprehensive review of lipoprotein function and their role in atherosclerosis, along with the latest development of lipoprotein targeted treatment, is timely. This review focuses on the functions of different lipoproteins and their involvement in atherosclerosis. Further, diagnostic and therapeutic potential are highlighted giving insight into novel lipoprotein-targetted approaches to treat atherosclerosis.
血脂异常的特征是脂质(胆固醇、甘油三酯或两者)水平升高,可增加动脉粥样硬化发生和进展的风险。随着动脉粥样硬化的进展,动脉斑块的数量和严重程度增加,心肌梗死风险增大,而心肌梗死是心血管死亡的主要原因。动脉粥样硬化的进展分为四个阶段,即内皮功能障碍、脂纹形成、病变进展和斑块破裂,最终导致血栓形成和动脉阻塞。随着对动脉粥样硬化潜在病理过程的深入了解,研究人员发现脂蛋白在动脉粥样硬化的发展中起重要作用。特别是,含载脂蛋白B(apoB)的脂蛋白已被证明与动脉粥样硬化有关。氧化型低密度脂蛋白(ox-LDL)也会促进动脉粥样硬化的进展,而高密度脂蛋白(HDL)则有助于从巨噬细胞中清除胆固醇,从而抑制泡沫细胞的形成。鉴于这些已知的关联,脂蛋白可能有潜力作为预测动脉粥样硬化斑块相关风险的生物标志物,或者可能成为新型治疗药物的靶点。因此,针对脂蛋白代谢的药物的快速发展可能会带来动脉粥样硬化的新疗法。及时对脂蛋白功能及其在动脉粥样硬化中的作用以及脂蛋白靶向治疗的最新进展进行全面综述很有必要。本综述重点关注不同脂蛋白的功能及其在动脉粥样硬化中的作用。此外,还强调了诊断和治疗潜力,深入探讨了治疗动脉粥样硬化的新型脂蛋白靶向方法。