Lookup NU author(s): Professor Quentin Anstee,
Professor Chris Day
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S-adenosyl-L-methionine (SAMe; Ado Met) is an important, metabolically pleiotropic molecule that participates in multiple cellular reactions as the precursor for the synthesis of glutathione and principle methyl donor required for methylation of nucleic acids, phospholipids, histones, biogenic amines, and proteins. SAMe synthesis is depressed in chronic liver disease and so there has been considerable interest in the utility of SAMe to ameliorate disease severity. Despite encouraging pre-clinical data confirming that SAMe depletion can exacerbate liver injury and supporting a hepatoprotective role for SAMe therapy, to date no large, high-quality randomised clinical trials have been performed that establish clinical utility in specific disease states. Here, we offer an in-depth review of the published scientific literature relating to the physiological and pathophysiological roles of SAMe and its therapeutic use in liver disease, critically assessing implications for clinical practice and offering recommendations for further research. (C) 2012 European Association for the Study of the Liver. Published by Elsevier B.V. All rights reserved.
Author(s): Anstee QM, Day CP
Publication type: Review
Publication status: Published
Journal: Journal of Hepatology
Print publication date: 01/11/2012
ISSN (print): 0168-8278
ISSN (electronic): 1600-0641
Publisher: ELSEVIER SCIENCE BV