| Literature DB >> 33477599 |
Anna Di Vito1, Annalidia Donato2, Ivan Presta2, Teresa Mancuso1, Francesco Saverio Brunetti2, Pasquale Mastroroberto1, Andrea Amorosi2, Natalia Malara1, Giuseppe Donato2.
Abstract
Calcific Aortic Valve Disease (CAVD) is the most common valvular heart disease in developed countries and in the ageing population. It is strongly correlated to median age, affecting up to 13% of the population over the age of 65. Pathophysiological analysis indicates CAVD as a result of an active and degenerative disease, starting with sclerosis and chronic inflammation and then leaflet calcification, which ultimately can account for aortic stenosis. Although CAVD has been firstly recognized as a passive event mostly resulting from a degenerative aging process, much evidences suggests that calcification arises from different active processes, involving both aortic valve-resident cells (valve endothelial cells, valve interstitial cells, mesenchymal stem cells, innate immunity cells) and circulating cells (circulating mesenchymal cells, immunity cells). Moreover, a role for the cell-derived "matrix vesicles" and extracellular matrix (ECM) components has also been recognized. The aim of this work is to review the cellular and molecular alterations occurring in aortic valve during CAVD pathogenesis, focusing on the role of ECM in the natural course of the disease.Entities:
Keywords: calcific aortic valve disease; collagen; elastic fibers; extracellular matrix; extracellular vesicles; periostin; tenascin-C
Year: 2021 PMID: 33477599 DOI: 10.3390/ijms22020913
Source DB: PubMed Journal: Int J Mol Sci ISSN: 1422-0067 Impact factor: 5.923