Drugs in devolopment: targeting high-density lipoprotein metabolism and raverse cholesterol transport

被引:25
作者
Duffy, D
Rader, DJ
机构
[1] Univ Penn, Sch Med, Inst Translat Med, Philadelphia, PA 19104 USA
[2] Univ Penn, Sch Med, Cardiovasc Inst, Philadelphia, PA 19104 USA
[3] Hosp Univ Penn, Dept Med, Philadelphia, PA 19104 USA
关键词
apoA-1; Milano; cholesteryl ester transfer protein; dual PPAR-alpha/PPAR-gamma agonist; fibrates; high-density lipoprotein; niacin; reverse cholesterol transport;
D O I
10.1097/01.hco.0000168532.69342.26
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Purpose of review This review summarizes currently available therapies for raising high-density lipoprotein cholesterol (HDL-C) and expands on therapies currently in development that target high-density lipoprotein cholesterol. Recent findings In the realm of new high-density lipoprotein-raising therapies, there is a strong focus on high-density lipoprotein metabolism and the reverse cholesterol transport pathway. Several infusions of recombinant apoA-I Milano/phospholipid complexes appeared to reduce atheroma volume as measured by intravascular ultrasound. Both intravenous and oral apoA-I mimetic peptides are in early clinical trials. Next generation PPAR-alpha agonists are more potent at high-density lipoprotein-raising than currently available fibrates, and dual PPAR-alpha/PPAR-gamma agonists are under investigation to help correct atherogenic dyslipidemia seen in many diabetics. Two small molecule inhibitors of the cholesteryl ester transfer protein have shown promise in clinical trials at substantially raising high-density lipoprotein cholesterol. Summary Larger scale clinical trials, including those with additional surrogate outcome measures as well as cardiovascular event outcomes are needed to further assess the benefit of newer high-density lipoprotein-raising therapies. Additional therapeutics are currently in development that target other parts of the reverse cholesterol transport pathway and, in addition to providing new potential pharmaceuticals, will help to further elucidate the atheroprotective mechanisms of high-density lipoprotein cholesterol.
引用
收藏
页码:301 / 306
页数:6
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