» Articles » PMID: 18047849

Increasing High-density Lipoprotein Cholesterol, Inhibition of Cholesteryl Ester Transfer Protein, and Heart Disease Risk Reduction

Overview
Journal Am J Cardiol
Date 2007 Dec 6
PMID 18047849
Citations 4
Authors
Affiliations
Soon will be listed here.
Abstract

Our purpose is to review recent research in the area of high-density lipoprotein (HDL) cholesterol raising and coronary artery disease (CAD) risk reduction. It is known that a decreased HDL cholesterol level is an important CAD risk factor and that raising HDL cholesterol has been associated with CAD risk reduction. A relative new strategy for raising HDL cholesterol, inhibition of cholesteryl ester transfer protein (CETP), is markedly effective. CETP inhibitors prevent the transfer of cholesteryl ester from HDL to triglyceride-rich lipoproteins in exchange for triglyceride. One inhibitor, torcetrapib, binds to CETP on HDL, markedly increases HDL cholesteryl ester, has no effect on fecal cholesterol excretion, but can raise blood pressure. A large clinical trial in patients with CAD who were taking atorvastatin was recently stopped prematurely because of excess mortality in those receiving torcetrapib versus placebo, and 2 other trials reported no benefit of torcetrapib on coronary atherosclerosis or carotid intima-media thickness as compared with subjects on atorvastatin alone. The adverse effects of torcetrapib may be compound specific, and because the crystal structure of CETP is now known, it should be possible to develop more optimal CETP inhibitors that do not form a nonproductive complex with CETP on the HDL particle, as has been reported for torcetrapib. Another alternative for increasing HDL levels is to develop more effective and better tolerated niacin preparations.

Citing Articles

HDL particle number and size as predictors of cardiovascular disease.

Kontush A Front Pharmacol. 2015; 6:218.

PMID: 26500551 PMC: 4593254. DOI: 10.3389/fphar.2015.00218.


Markers of Systemic Inflammation and Apo-AI Containing HDL Subpopulations in Women with and without Diabetes.

Russo G, Giandalia A, Romeo E, Alibrandi A, Horvath K, Asztalos B Int J Endocrinol. 2014; 2014:607924.

PMID: 25258627 PMC: 4167212. DOI: 10.1155/2014/607924.


Docking and molecular dynamics study on the inhibitory activity of N, N-disubstituted-trifluoro-3-amino-2-propanols-based inhibitors of cholesteryl ester transfer protein.

Dong B, Liao Q, Wei J J Mol Model. 2010; 17(7):1727-34.

PMID: 21057835 DOI: 10.1007/s00894-010-0881-7.


Cholesteryl ester transfer protein: at the heart of the action of lipid-modulating therapy with statins, fibrates, niacin, and cholesteryl ester transfer protein inhibitors.

Chapman M, Le Goff W, Guerin M, Kontush A Eur Heart J. 2009; 31(2):149-64.

PMID: 19825813 PMC: 2806550. DOI: 10.1093/eurheartj/ehp399.