TY - JOUR
T1 - Effect of Subject-Specific, Spatially Reduced, and Idealized Boundary Conditions on the Predicted Hemodynamic Environment in the Murine Aorta
AU - Smith, Kelly A.
AU - Merchant, Samer S.
AU - Hsu, Edward W.
AU - Timmins, Lucas H.
N1 - Funding Information:
MRI scans were performed at the University of Utah Preclinical Imaging Facility supported by NIH Grant S10 RR023017. Seg3D is an Open Source software project that is supported by the National Institute of General Medical Sciences of the National Institutes of Health under Grant Number P41 GM103545.
Publisher Copyright:
© 2021, Biomedical Engineering Society.
PY - 2021/12
Y1 - 2021/12
N2 - Mouse models of atherosclerosis have become effective resources to study atherogenesis, including the relationship between hemodynamics and lesion development. Computational methods aid the prediction of the in vivo hemodynamic environment in the mouse vasculature, but careful selection of inflow and outflow boundary conditions (BCs) is warranted to promote model accuracy. Herein, we investigated the impact of animal-specific versus reduced/idealized flow boundary conditions on predicted blood flow patterns in the mouse thoracic aorta. Blood velocities were measured in the aortic root, arch branch vessel, and descending aorta in ApoE−/− mice using phase-contrast MRI. Computational geometries were derived from micro-CT imaging and combinations of high-fidelity or reduced/idealized MR-derived BCs were applied to predict the bulk flow field and hemodynamic metrics (e.g., wall shear stress, WSS; cross-flow index, CFI). Results demonstrate that pressure-free outlet BCs significantly overestimate outlet flow rates as compared to measured values. When compared to models that incorporate 3-component inlet velocity data [v⇀ (vr, vθ, vz)] and time-varying outlet mass flow splits [Q(t)] (i.e., high-fidelity model), neglecting in-plane inlet velocity components (i.e., v⇀ (vz)) leads to errors in WSS and CFI values ranging from 10 to 30% across the model domain whereas the application of a steady outlet mass flow splits results in negligible differences in these hemodynamics metrics. This investigation highlights that 3-component inlet velocity data and at least steady mass flow splits are required for accurate predictions of flow patterns in the mouse thoracic aorta.
AB - Mouse models of atherosclerosis have become effective resources to study atherogenesis, including the relationship between hemodynamics and lesion development. Computational methods aid the prediction of the in vivo hemodynamic environment in the mouse vasculature, but careful selection of inflow and outflow boundary conditions (BCs) is warranted to promote model accuracy. Herein, we investigated the impact of animal-specific versus reduced/idealized flow boundary conditions on predicted blood flow patterns in the mouse thoracic aorta. Blood velocities were measured in the aortic root, arch branch vessel, and descending aorta in ApoE−/− mice using phase-contrast MRI. Computational geometries were derived from micro-CT imaging and combinations of high-fidelity or reduced/idealized MR-derived BCs were applied to predict the bulk flow field and hemodynamic metrics (e.g., wall shear stress, WSS; cross-flow index, CFI). Results demonstrate that pressure-free outlet BCs significantly overestimate outlet flow rates as compared to measured values. When compared to models that incorporate 3-component inlet velocity data [v⇀ (vr, vθ, vz)] and time-varying outlet mass flow splits [Q(t)] (i.e., high-fidelity model), neglecting in-plane inlet velocity components (i.e., v⇀ (vz)) leads to errors in WSS and CFI values ranging from 10 to 30% across the model domain whereas the application of a steady outlet mass flow splits results in negligible differences in these hemodynamics metrics. This investigation highlights that 3-component inlet velocity data and at least steady mass flow splits are required for accurate predictions of flow patterns in the mouse thoracic aorta.
KW - Atherosclerosis
KW - Blood flow
KW - Computational fluid dynamics
KW - Imaging
KW - Mouse
KW - Phase contract MRI
KW - Wall shear stress
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U2 - 10.1007/s10439-021-02851-7
DO - 10.1007/s10439-021-02851-7
M3 - Article
C2 - 34528150
AN - SCOPUS:85114915556
SN - 0090-6964
VL - 49
SP - 3255
EP - 3266
JO - Annals of Biomedical Engineering
JF - Annals of Biomedical Engineering
IS - 12
ER -