Weinberg Eli J, Kaazempur Mofrad Mohammad R
Department of Bioengineering, University of California Berkeley, CA, USA.
J Biomech. 2008 Dec 5;41(16):3482-7. doi: 10.1016/j.jbiomech.2008.08.006. Epub 2008 Nov 8.
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.
与具有正常三尖瓣主动脉瓣(TAV)的人群相比,患有二叶式主动脉瓣(BAV)的患者更有可能发展为钙化性主动脉瓣狭窄(CAS)以及许多其他疾病。目前尚不清楚CAS风险的增加是由三尖瓣和二叶式瓣膜之间的几何差异引起的,还是由产生几何差异的相同潜在因素引起的。CAS进展被认为是一个多尺度过程,在细胞水平上介导。在本研究中,我们采用瓣膜的多尺度有限元模拟。我们分离出一个几何因素——瓣叶数量的影响,以探索其对多尺度瓣膜力学的影响,特别是与CAS相关的影响。通过一组描述细胞、组织和器官长度尺度的模拟对BAV和TAV进行建模。这些模拟在长度尺度之间相互关联,以创建一个连贯的多尺度模型。在每个尺度上,模型都是三维动态的,并纳入了瓣膜小叶组织的精确非线性本构模型。我们比较了每个长度尺度上TAV和BAV之间的结果。在细胞尺度上,我们感兴趣的区域是小叶主动脉面附近钙化发生的位置。我们的模拟显示了在器官尺度上三尖瓣和二叶式瓣膜之间观察到的差异:相对于三尖瓣,二叶式瓣膜在固相显示出更大的弯曲,在液相显示出更强的射流形成。然而,在细胞尺度上,我们表明感兴趣的区域通过纤维层的褶皱免受应变影响。因此,在易钙化区域,TAV和BAV之间的细胞变形没有显著差异。这一结果支持了这样的观点,即BAV与TAV中观察到的钙化差异可能主要归因于除两个瓣膜之间简单几何差异之外的因素。