Mathematical Modeling and Analysis of Atherosclerosis Based on Fluid‐Multilayered Poroelastic Structure Interaction Model

ABSTRACT In this paper, we establish a model of atherosclerosis in the early stage based on fluid‐structure interaction (FSI) model of blood vessel and prove the existence of weak solutions. The model consists of Navier–Stokes equation, Biot equations, and reaction–diffusion equations, which involves the effect of blood flow velocity on the concentration of low‐density lipoprotein (LDL) and other biological components. We first divide the model into an FSI submodel and a coupled reaction–diffusion submodel, respectively. Then, by using Rothe's method and operator splitting numerical scheme, we obtain the existence of weak solution of FSI submodel. In order to solve the nonlinear term representing the consumption of oxidized low‐density lipoprotein (oxLDL), we construct a regular system. The results in FSI submodel together with Schauder's fixed‐point theorem allow us to obtain the existence of nonnegative weak solutions for the reaction–diffusion submodel by showing the existence and nonnegativity of weak solutions for the regular system. Numerical simulations were performed in an idealized two‐dimensional geometry in order to verify that vascular narrowing caused by plaque further exacerbates plaque growth.

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Publication Details

Journal
Studies in Applied Mathematics
Published
2025-03-01
DOI
https://doi.org/10.1111/sapm.70028
Primary Topic
Biomarkers in Disease Mechanisms
Type
article
Field-Weighted Citation Impact
0.00

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article

Mathematical Modeling and Analysis of Atherosclerosis Based on Fluid‐Multilayered Poroelastic Structure Interaction Model

Yanning An, Wenjun Liu
Studies in Applied Mathematics
Biomarkers in Disease Mechanisms
article

Mathematical Modeling and Analysis of Atherosclerosis Based on Fluid‐Multilayered Poroelastic Structure Interaction Model

Yanning An, Wenjun Liu
article en

Abstract

ABSTRACT In this paper, we establish a model of atherosclerosis in the early stage based on fluid‐structure interaction (FSI) model of blood vessel and prove the existence of weak solutions. The model consists of Navier–Stokes equation, Biot equations, and reaction–diffusion equations, which involves the effect of blood flow velocity on the concentration of low‐density lipoprotein (LDL) and other biological components. We first divide the model into an FSI submodel and a coupled reaction–diffusion submodel, respectively. Then, by using Rothe's method and operator splitting numerical scheme, we obtain the existence of weak solution of FSI submodel. In order to solve the nonlinear term representing the consumption of oxidized low‐density lipoprotein (oxLDL), we construct a regular system. The results in FSI submodel together with Schauder's fixed‐point theorem allow us to obtain the existence of nonnegative weak solutions for the reaction–diffusion submodel by showing the existence and nonnegativity of weak solutions for the regular system. Numerical simulations were performed in an idealized two‐dimensional geometry in order to verify that vascular narrowing caused by plaque further exacerbates plaque growth.

Studies in Applied MathematicsVol. 154(3)
Nanjing University of Information Science and Technology (CN)
National Natural Science Foundation of China
Openalex Percentile: Top 95%
Biomarkers in Disease Mechanisms
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