Mechanical and Biochemical Simulations of Atherosclerosis
ORAL
Abstract
Atherosclerosis is a disease considered to be one of the leading causes of death. Understanding the behavior and dynamics of the vessel wall before and after atherosclerosis has been a motivation for many studies.
We investigate this phenomenon as a combination of mechanical deformation of the vessel wall along with the cell and chemical dynamics that happen inside of it.
We consider the vessel wall as a growing hyperelastic material with three layers, each having a different set of mechanical properties. To describe tissue growth we use morphoelasticity as the mathematical framework. To include the stiffening effect of collagen fibers we employ a Holzapfel-Gasser-Ogden anisotropic strain energy function.
In addition, we explore the distribution of oxidized lipids, macrophages, foam cells, oxygen and necrotic cells in the intima at each growth step via a system of PDEs.
All numerical simulations are carried out via the finite element method on the FENICS framework.
Altogether, this allows us to observe intimal thickening as a result of vessel growth along with histological changes within the wall such as the development of necrotic zones. Our simulations show results similar to the images acquired from ultrasounds scans.
We investigate this phenomenon as a combination of mechanical deformation of the vessel wall along with the cell and chemical dynamics that happen inside of it.
We consider the vessel wall as a growing hyperelastic material with three layers, each having a different set of mechanical properties. To describe tissue growth we use morphoelasticity as the mathematical framework. To include the stiffening effect of collagen fibers we employ a Holzapfel-Gasser-Ogden anisotropic strain energy function.
In addition, we explore the distribution of oxidized lipids, macrophages, foam cells, oxygen and necrotic cells in the intima at each growth step via a system of PDEs.
All numerical simulations are carried out via the finite element method on the FENICS framework.
Altogether, this allows us to observe intimal thickening as a result of vessel growth along with histological changes within the wall such as the development of necrotic zones. Our simulations show results similar to the images acquired from ultrasounds scans.
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Presenters
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Navid Mohammad Mirzaei
University of Delaware
Authors
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Navid Mohammad Mirzaei
University of Delaware
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Pak-Wing Fok
University of Delaware