Investigational drugs targeting HDL-C metabolism and reverse cholesterol transport

被引:8
作者
Robinson, Jennifer G.
Davidson, Michael H.
机构
[1] Univ Iowa, Coll Publ Hlth, Lipid Res Clin, Dept Epidemiol, Iowa City, IA 52242 USA
[2] Univ Iowa, Coll Med, Dept Med, Lipid Res Clin, Iowa City, IA 52242 USA
来源
FUTURE LIPIDOLOGY | 2007年 / 2卷 / 03期
关键词
cardiovascular disease; emerging therapies; high-density lipoprotein; cholesterol; mechanisms; prevention;
D O I
10.2217/17460875.2.3.285
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Low high-density lipoprotein cholesterol (HDL-C) levels are associated with higher risk of cardiovascular disease, even in patients receiving statin therapy. HDL-C has a number of potential atheroprotective mechanisms, including reverse cholesterol transport. HDL-C also has antioxidant, anti-inflammatory, vasodilatory and antithrombotic effects. A number of targets with the potential to raise HDL-C levels and/or increase reverse cholesterol transport have been identified. Plasma concentrations of HDL-C are the net result of the de novo production, catabolism and recycling of HDL-C particles, as well as the contribution to HDL-C from components of other lipoproteins. HDL-C levels can be modified by increasing the production of apolipoprotein A-I or by delaying the clearance of HDL-C from the plasma. Whether manipulation of these drug targets to raise HDL-C will result in cardiovascular event reduction remains to be determined.
引用
收藏
页码:285 / 301
页数:17
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