Division of Translational Medicine and Human Genetics, Perelman School of Medicine at the University of Pennsylvania, Philadelphia, Pennsylvania, USA.
Clin Pharmacol Ther. 2014 Jul;96(1):48-56. doi: 10.1038/clpt.2014.79. Epub 2014 Apr 8.
High-density-lipoprotein cholesterol (HDL-C) has been identified in population studies as an independent inverse predictor of cardiovascular events. Although the causal nature of this association has been questioned, HDL and its major protein, apolipoprotein (apo)A1, have been shown to prevent and reverse atherosclerosis in animal models. In addition, HDL and apoA1 have several putatively atheroprotective functions, such as the ability to promote efflux of cholesterol from macrophages in the artery wall, inhibit vascular inflammation, and enhance endothelial function. Therefore, HDL-C and apoA1 have been investigated as therapeutic targets for coronary heart disease. However, recent clinical trials with drugs that raise HDL-C, such as niacin and inhibitors of cholesteryl ester transfer protein, have been disappointing. Here, we review the current state of the science regarding HDL as a therapeutic target.
高密度脂蛋白胆固醇(HDL-C)在人群研究中被确定为心血管事件的独立负向预测因子。尽管这种关联的因果关系受到质疑,但已经证明 HDL 及其主要蛋白质载脂蛋白(apo)A1 可以在动物模型中预防和逆转动脉粥样硬化。此外,HDL 和 apoA1 具有几种据称具有抗动脉粥样硬化的功能,例如促进动脉壁中巨噬细胞中胆固醇的流出、抑制血管炎症和增强内皮功能的能力。因此,HDL-C 和 apoA1 已被作为冠心病的治疗靶点进行研究。然而,最近用升高 HDL-C 的药物(如烟酸和胆固醇酯转移蛋白抑制剂)进行的临床试验令人失望。在这里,我们回顾了关于 HDL 作为治疗靶点的科学现状。