Non-cholesterol sterols and cholesterol metabolism in sitosterolemia.

Rgia A Othman, Semone B Myrie, Peter J H Jones

Journal: Atherosclerosis 2014;231(2):291-9

PMID: 24267242

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Abstract

Sitosterolemia (STSL) is a rare autosomal recessive disease, manifested by extremely elevated plant sterols (PS) in plasma and tissue, leading to xanthoma and premature atherosclerotic disease. Therapeutic approaches include limiting PS intake, interrupting enterohepatic circulation of bile acid using bile acid binding resins such as cholestyramine, and/or ileal bypass, and inhibiting intestinal sterol absorption by ezetimibe (EZE). The objective of this review is to evaluate sterol metabolism in STSL and the impact of the currently available treatments on sterol trafficking in this disease. The role of PS in initiation of xanthomas and premature atherosclerosis is also discussed. Blocking sterols absorption with EZE has revolutionized STSL patient treatment as it reduces circulating levels of non-cholesterol sterols in STSL. However, none of the available treatments including EZE have normalized plasma PS concentrations. Future studies are needed to: (i) explore where cholesterol and non-cholesterol sterols accumulate, (ii) assess to what extent these sterols in tissues can be mobilized after blocking their absorption, and (iii) define the factors governing sterol flux.

Address: Department of Human Nutritional Sciences, University of Manitoba, Winnipeg, Manitoba, Canada; Richardson Centre for Functional Foods and Nutraceuticals, University of Manitoba, Winnipeg, Manitoba, Canada.

DOI: 10.1016/j.atherosclerosis.2013.09.038

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MeSH Terms: ATP Binding Cassette Transporter, Subfamily G, ATP-Binding Cassette Transporters, Absorption, Atherosclerosis, Azetidines, Cholesterol, Disease Progression, Ezetimibe, Humans, Hypercholesterolemia, Intestinal Diseases, Kinetics, Lipid Metabolism, Inborn Errors, Membrane Proteins, Membrane Transport Proteins, Phytosterols, Sitosterols, Sterol O-Acyltransferase, Sterols, Xanthomatosis, Sterol O-Acyltransferase 2