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Isolation of Mouse Interstitial Valve Cells to Study the Calcification of the Aortic Valve In Vitro
Published on: May 10, 2021
A multiscale computational comparison of the bicuspid and tricuspid aortic valves in relation to calcific aortic
Eli J Weinberg1, Mohammad R Kaazempur Mofrad
1Department of Bioengineering, University of California Berkeley, CA, USA.
Insights
Bicuspid aortic valves (BAV) show increased calcific aortic stenosis (CAS) risk. Multiscale simulations suggest valve geometry alone may not explain this CAS risk difference between BAV and tricuspid aortic valves (TAV).
Area of Science:
- Biomedical Engineering
- Computational Biology
- Cardiovascular Research
Background:
- Patients with bicuspid aortic valve (BAV) have a higher incidence of calcific aortic stenosis (CAS) compared to those with normal tricuspid aortic valves (TAV).
- The underlying cause for this increased CAS risk in BAV patients—whether due to valve geometry or shared etiological factors—remains unclear.
Purpose of the Study:
- To investigate the influence of aortic valve cusp number on the mechanics of calcific aortic stenosis (CAS) progression.
- To differentiate the contributions of geometric factors versus other underlying causes to CAS development in bicuspid aortic valves (BAV).
Main Methods:
- Employed multiscale finite-element simulations modeling cell, tissue, and organ length scales for both bicuspid aortic valves (BAV) and tricuspid aortic valves (TAV).
- Incorporated three-dimensional, dynamic models with nonlinear constitutive laws for valve leaflet tissue.
- Linked simulations across scales to create a comprehensive multiscale model, comparing BAV and TAV under various conditions.
Main Results:
- Organ-scale simulations revealed greater leaflet flexure and stronger fluid jet formation in the bicuspid aortic valve (BAV) compared to the tricuspid aortic valve (TAV).
- Cell-scale simulations indicated that fibrosa wrinkling shields the calcification-prone region, resulting in no significant difference in cellular deformation between BAV and TAV.
- The study found that cellular deformations in the calcification-prone region were not significantly different between bicuspid aortic valves (BAV) and tricuspid aortic valves (TAV).
Conclusions:
- The geometric difference between bicuspid aortic valves (BAV) and tricuspid aortic valves (TAV) alone may not be the primary driver of increased calcific aortic stenosis (CAS) risk in BAV.
- Other underlying factors, not solely related to valve geometry, likely contribute significantly to the higher prevalence of CAS in patients with bicuspid aortic valves (BAV).
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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