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Glycosaminoglycan synthesis and structure as targets for the prevention of calcific aortic valve disease

Journal

CARDIOVASCULAR RESEARCH
Volume 76, Issue 1, Pages 19-28

Publisher

OXFORD UNIV PRESS
DOI: 10.1016/j.cardiores.2007.05.014

Keywords

calcific aortic valve disease; proteoglycans; hyaluronan; lipid retention; inflammation

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Calcific aortic valve disease is frequently driven by ageing and the obesity-associated metabolic syndrome, and the increasing impact of these factors indicates that valve disease will become a cardiovascular disease of considerable significance. This disease is now thought to be an active cell-based disease process, which may therefore be amenable to therapeutic intervention. Some similarities are apparent with atherosclerosis. The accumulation of lipid, possibly by retention by proteoglycans and the attraction of inflammatory cells by hyaluronan, may be common to the early stages of both pathologies. The synthesis and structure of glycosaminoglycans, proteoglycans, and hyaluronan are exquisitely regulated, and the signalling pathways controlling these processes may provide tissue-specific opportunities for concomitant prevention of atherosclerosis and calcific aortic valve disease. (C) 2007 European Society of Cardiology. Published by Elsevier B.V. All rights reserved.

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