Literature DB >> 18996528

A multiscale computational comparison of the bicuspid and tricuspid aortic valves in relation to calcific aortic stenosis.

Eli J Weinberg1, Mohammad R Kaazempur Mofrad.   

Abstract

Patients with bicuspid aortic valve (BAV) are more likely to develop a calcific aortic stenosis (CAS), as well as a number of other ailments, as compared to their cohorts with normal tricuspid aortic valves (TAV). It is currently unknown whether the increase in risk of CAS is caused by the geometric differences between the tricuspid and bicuspid valves or whether the increase in risk is caused by the same underlying factors that produce the geometric difference. CAS progression is understood to be a multiscale process, mediated at the cell level. In this study, we employ multiscale finite-element simulations of the valves. We isolate the effect of one geometric factor, the number of cusps, in order to explore its effect on multiscale valve mechanics, particularly in relation to CAS. The BAV and TAV are modeled by a set of simulations describing the cell, tissue, and organ length scales. These simulations are linked across the length scales to create a coherent multiscale model. At each scale, the models are three-dimensional, dynamic, and incorporate accurate nonlinear constitutive models of the valve leaflet tissue. We compare results between the TAV and BAV at each length scale. At the cell-scale, our region of interest is the location where calcification develops, near the aortic-facing surface of the leaflet. Our simulations show the observed differences between the tricuspid and bicuspid valves at the organ scale: the bicuspid valve shows greater flexure in the solid phase and stronger jet formation in the fluid phase relative to the tricuspid. At the cell-scale, however, we show that the region of interest is shielded against strain by the wrinkling of the fibrosa. Thus, the cellular deformations are not significantly different between the TAV and BAV in the calcification-prone region. This result supports the assertion that the difference in calcification observed in the BAV versus TAV may be due primarily to factors other than the simple geometric difference between the two valves.

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Year:  2008        PMID: 18996528     DOI: 10.1016/j.jbiomech.2008.08.006

Source DB:  PubMed          Journal:  J Biomech        ISSN: 0021-9290            Impact factor:   2.712


  27 in total

1.  Cyclic strain anisotropy regulates valvular interstitial cell phenotype and tissue remodeling in three-dimensional culture.

Authors:  Russell A Gould; Karen Chin; Thom P Santisakultarm; Amanda Dropkin; Jennifer M Richards; Chris B Schaffer; Jonathan T Butcher
Journal:  Acta Biomater       Date:  2012-01-11       Impact factor: 8.947

2.  Fluid-structure interaction modeling of calcific aortic valve disease using patient-specific three-dimensional calcification scans.

Authors:  Rotem Halevi; Ashraf Hamdan; Gil Marom; Karin Lavon; Sagit Ben-Zekry; Ehud Raanani; Danny Bluestein; Rami Haj-Ali
Journal:  Med Biol Eng Comput       Date:  2016-02-23       Impact factor: 2.602

Review 3.  In vivo imaging and computational analysis of the aortic root. Application in clinical research and design of transcatheter aortic valve systems.

Authors:  Paul Schoenhagen; Alexander Hill; Tim Kelley; Zoran Popovic; Sandra S Halliburton
Journal:  J Cardiovasc Transl Res       Date:  2011-04-12       Impact factor: 4.132

4.  Fully coupled fluid-structure interaction model of congenital bicuspid aortic valves: effect of asymmetry on hemodynamics.

Authors:  Gil Marom; Hee-Sun Kim; Moshe Rosenfeld; Ehud Raanani; Rami Haj-Ali
Journal:  Med Biol Eng Comput       Date:  2013-03-10       Impact factor: 2.602

5.  Effect of Geometry on the Leaflet Stresses in Simulated Models of Congenital Bicuspid Aortic Valves.

Authors:  Paul N Jermihov; Lu Jia; Michael S Sacks; Robert C Gorman; Joseph H Gorman; Krishnan B Chandran
Journal:  Cardiovasc Eng Technol       Date:  2011-03       Impact factor: 2.495

6.  The role of stress concentration in calcified bicuspid aortic valve.

Authors:  Tongran Qin; Andrés Caballero; Wenbin Mao; Brian Barrett; Norihiko Kamioka; Stamatios Lerakis; Wei Sun
Journal:  J R Soc Interface       Date:  2020-06-10       Impact factor: 4.118

Review 7.  Computational modeling of cardiac valve function and intervention.

Authors:  Wei Sun; Caitlin Martin; Thuy Pham
Journal:  Annu Rev Biomed Eng       Date:  2014-04-16       Impact factor: 9.590

8.  Immersed boundary-finite element model of fluid-structure interaction in the aortic root.

Authors:  Vittoria Flamini; Abe DeAnda; Boyce E Griffith
Journal:  Theor Comput Fluid Dyn       Date:  2015-12-19       Impact factor: 1.606

Review 9.  Mechanisms of calcification in aortic valve disease: role of mechanokinetics and mechanodynamics.

Authors:  W David Merryman; Frederick J Schoen
Journal:  Curr Cardiol Rep       Date:  2013-05       Impact factor: 2.931

10.  Hemodynamic environments from opposing sides of human aortic valve leaflets evoke distinct endothelial phenotypes in vitro.

Authors:  Eli J Weinberg; Peter J Mack; Frederick J Schoen; Guillermo García-Cardeña; Mohammad R Kaazempur Mofrad
Journal:  Cardiovasc Eng       Date:  2010-03
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