Summary
November 2006, Vol. 15, No. 11, Pages 1337-1351 , DOI 10.1517/13543784.15.11.1337

Cholesterol absorption inhibitors as a therapeutic option for hypercholesterolaemia

John R Burnett1,2 & Murray W Huff3,4
1Royal Perth Hospital, Department of Core Clinical Pathology & Biochemistry, PathWest Laboratory Medicine WA, Wellington Street Campus, GPO Box X2213, Perth, WA 6847, Australia.
2University of Western Australia, School of Medicine & Pharmacology, Australia
3Robarts Research Institute, Vascular Biology Group, 100 Perth Drive, London, Ontario N6A 5K8, Canada
4University of Western Ontario, Departments of Medicine and Biochemistry, London, Ontario, Canada
Author for correspondence



The development of cholesterol-lowering drugs (including a variety of statins, bile acid-binding resins and recently discovered inhibitors of cholesterol absorption) has expanded the options for cardiovascular prevention. Recent treatment guidelines emphasise that individuals at substantial risk for atherosclerotic coronary heart disease should meet defined targets for LDL cholesterol concentrations. Combination therapy with drugs that have different or complementary mechanisms of action is often needed to achieve lipid goals. Existing approaches to the treatment of hypercholesterolaemia are still ineffective in halting the progression of coronary artery disease in some patients despite combination therapies. Other patients are resistant to conventional drug treatment and remain at high risk for the development and progression of atherosclerotic cardiovascular disease and alternative approaches are needed. The discovery and development of ezetimibe (a novel, selective and potent cholesterol absorption inhibitor) has advanced the treatment of hypercholesterolaemia. New agents including the phytostanol preparation FM-VP4 and inhibitors of acyl coenzyme A:cholesterol acyltransferase, the apical Na+-dependent bile acid transporter and microsomal triglyceride transfer protein may also play a future role in combination therapy. This review focuses on the recent progress in the molecular mechanisms of intestinal cholesterol absorption and transport, and novel therapeutic approaches to inhibit the cholesterol absorption process.

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Forward Links to Citing Articles

Rebecca L Pollex, Tisha R Joy, Robert A Hegele. (2008) Emerging antidyslipidemic drugs. Expert Opinion on Emerging Drugs 13:2, 363-381
Online publication date: 1-Jun-2008.
Summary | Full Text | PDF (683 KB) | PDF Plus (816 KB) 
John R Burnett, Gerald F Watts. (2007) MTP inhibition as a treatment for dyslipidaemias: time to deliver or empty promises?. Expert Opinion on Therapeutic Targets 11:2, 181-189
Online publication date: 1-Feb-2007.
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Authors:
John R Burnett
Murray W Huff
Keywords:
ACAT inhibitor
ASBT inhibitor
bile acid-binding resin
cholesterol absorption
cholesterol transport
ezetimibe
FM-VP4
MTP inhibitor
NPC1L1