| Literature DB >> 25249188 |
Meghan A Bowler1, W David Merryman2.
Abstract
Calcific aortic valve disease (CAVD) affects 25% of people over 65, and the late-stage stenotic state can only be treated with total valve replacement, requiring 85,000 surgeries annually in the US alone (University of Maryland Medical Center, 2013, http://umm.edu/programs/services/heart-center-programs/cardiothoracic-surgery/valve-surgery/facts). As CAVD is an age-related disease, many of the affected patients are unable to undergo the open-chest surgery that is its only current cure. This challenge motivates the elucidation of the mechanisms involved in calcification, with the eventual goal of alternative preventative and therapeutic strategies. There is no sufficient animal model of CAVD, so we turn to potential in vitro models. In general, in vitro models have the advantages of shortened experiment time and better control over multiple variables compared to in vivo models. As with all models, the hypothesis being tested dictates the most important characteristics of the in vivo physiology to recapitulate. Here, we collate the relevant pieces of designing and evaluating aortic valve calcification so that investigators can more effectively draw significant conclusions from their results.Entities:
Keywords: Calcific aortic valve disease; In vitro; Model; Quantification methods
Mesh:
Year: 2014 PMID: 25249188 PMCID: PMC4268061 DOI: 10.1016/j.carpath.2014.08.003
Source DB: PubMed Journal: Cardiovasc Pathol ISSN: 1054-8807 Impact factor: 2.185