Temporal geometric mapping defines morphoelastic growth model of Type B aortic dissection evolution

The human aorta undergoes complex morphologic changes that mirror the evolution of disease. Finite element analysis (FEA) enables the prediction of aortic pathologic states, but the absence of a biomechanical understanding hinders the applicability of this computational tool. We incorporate geometric information from computed tomography angiography (CTA) imaging scans into FEA to predict a trajectory of future geometries for four aortic disease patients. Through defining a geometric correspondence between two patient scans separated in time, a patient-specific FEA model can recreate the deformation of the aorta between the two time points, showing that pathologic growth drives morphologic heterogeneity. FEA-derived trajectories in a shape-size geometric feature space, which plots the variance of the shape index versus the inverse square root of aortic surface area (δS vs. [Formula: see text] ), quantitatively demonstrate an increase in δS. This represents a deviation from physiologic shape changes and parallels the true geometric progression of aortic disease patients.

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Publication Details

Journal
Computers in Biology and Medicine
Published
2024-09-27
DOI
https://doi.org/10.1016/j.compbiomed.2024.109194
Citations
1
Primary Topic
Aortic Disease and Treatment Approaches
Type
article
Field-Weighted Citation Impact
0.42

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article

Temporal geometric mapping defines morphoelastic growth model of Type B aortic dissection evolution

Junsung Kim, Nhung Nguyen, Ross Milner, Kameel Khabaz et al.
1 citations
Computers in Biology and Medicine
Aortic Disease and Treatment Approaches
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article

Temporal geometric mapping defines morphoelastic growth model of Type B aortic dissection evolution

Junsung Kim, Nhung Nguyen, Ross Milner, Kameel Khabaz, Luka Pocivavsek
article en
1 citations

Abstract

The human aorta undergoes complex morphologic changes that mirror the evolution of disease. Finite element analysis (FEA) enables the prediction of aortic pathologic states, but the absence of a biomechanical understanding hinders the applicability of this computational tool. We incorporate geometric information from computed tomography angiography (CTA) imaging scans into FEA to predict a trajectory of future geometries for four aortic disease patients. Through defining a geometric correspondence between two patient scans separated in time, a patient-specific FEA model can recreate the deformation of the aorta between the two time points, showing that pathologic growth drives morphologic heterogeneity. FEA-derived trajectories in a shape-size geometric feature space, which plots the variance of the shape index versus the inverse square root of aortic surface area (δS vs. [Formula: see text] ), quantitatively demonstrate an increase in δS. This represents a deviation from physiologic shape changes and parallels the true geometric progression of aortic disease patients.

Computers in Biology and MedicineVol. 182
University of California, Los Angeles (US), University of Chicago (US)
University of Chicago, Georgia Clinical and Translational Science Alliance, National Institutes of Health, National Heart, Lung, and Blood Institute
Openalex Percentile: Top 33%
Aortic Disease and Treatment Approaches
0.42
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