Fluid-structure interaction simulation of tissue degradation and its effects on intra-aneurysm hemodynamics

  • Tissue degradation plays a crucial role in vascular diseases such as atherosclerosis and aneurysms. Computational modeling of vascular hemodynamics incorporating both arterial wall mechanics and tissue degradation has been a challenging task. In this study, we propose a novel finite element method-based approach to model the microscopic degradation of arterial walls and its interaction with blood flow. The model is applied to study the combined effects of pulsatile flow and tissue degradation on the deformation and intra-aneurysm hemodynamics. Our computational analysis reveals that tissue degradation leads to a weakening of the aneurysmal wall, which manifests itself in a larger deformation and a smaller von Mises stress. Moreover, simulation results for different heart rates, blood pressures and aneurysm geometries indicate consistently that, upon tissue degradation, wall shear stress increases near the flow-impingement region and decreases away from it. These findings are discussed in the context of recent reports regarding the role of both high and low wall shear stress for the progression and rupture of aneurysms.

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Metadaten
Author:Haifeng WangORCiDGND, Klemens UhlmannORCiDGND, Vijay VedulaGND, Daniel BalzaniORCiDGND, Fathollah VarnikORCiDGND
URN:urn:nbn:de:hbz:294-86166
DOI:https://doi.org/10.1007/s10237-022-01556-7
Parent Title (English):Biomechanics and modeling in mechanobiology
Publisher:Springer
Place of publication:Berlin
Document Type:Article
Language:English
Date of Publication (online):2022/02/18
Date of first Publication:2022/01/13
Publishing Institution:Ruhr-Universität Bochum, Universitätsbibliothek
Tag:Aneurysm; Fluid-structure interaction (FSI); Hemodynamics; Tissue degradation
Volume:21
First Page:671
Last Page:683
Institutes/Facilities:Interdisciplinary Centre for Advanced Materials Simulation (ICAMS)
open_access (DINI-Set):open_access
Licence (English):License LogoCreative Commons - CC BY 4.0 - Attribution 4.0 International