Clinical trials with cholesteryl ester transfer protein inhibitors

被引:16
作者
Di Bartolo, Belinda A. [1 ]
Duong, MyNgan [1 ]
Nicholls, Stephen J. [1 ]
机构
[1] Univ Adelaide, South Australian Hlth & Med Res Inst, Adelaide, SA, Australia
关键词
cardiovascular disease; cholesteryl ester transfer protein; clinical trials; lipids; risk factors; HIGH-DENSITY-LIPOPROTEIN; CORONARY-HEART-DISEASE; LIPID-LEVEL MANAGEMENT; EVENTS ILLUMINATE TRIAL; HIGH-RISK; DOUBLE-BLIND; FAMILIAL HYPERCHOLESTEROLEMIA; CETP ACTIVITY; ATHEROSCLEROSIS; TORCETRAPIB;
D O I
10.1097/MOL.0000000000000352
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
Purpose of review Inhibition of cholesteryl ester transfer protein (CETP) has received considerable interest by virtue of its favorable effects on atherogenic and protective lipid parameters. The impact of CETP inhibitors in large clinical outcome trials will be reviewed. Recent findings Population and genetic studies demonstrate that low CETP activity associates with lower rates of cardiovascular events. Inhibiting CETP activity in animal models has a favorable impact on experimental atherosclerosis. Although the first CETP inhibitor to advance to an outcome trial proved to have adverse clinical effects and the next agent, a more modest inhibitor, was clinically futile, there continues to be immense interest in the potential to develop nontoxic, potent CETP inhibitors to reduce cardiovascular risk. Summary The current status of CETP inhibitors in the context of large outcomes trials will be reviewed.
引用
收藏
页码:545 / 549
页数:5
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