Data-driven generation of 4D velocity profiles in the aneurysmal ascending aorta.

4D Flow magnetic resonance imaging Aortic velocity profile Ascending aortic aneurysm Inflow boundary conditions Statistical shape modeling

Journal

Computer methods and programs in biomedicine
ISSN: 1872-7565
Titre abrégé: Comput Methods Programs Biomed
Pays: Ireland
ID NLM: 8506513

Informations de publication

Date de publication:
May 2023
Historique:
received: 02 11 2022
revised: 15 02 2023
accepted: 05 03 2023
medline: 11 4 2023
pubmed: 16 3 2023
entrez: 15 3 2023
Statut: ppublish

Résumé

Numerical simulations of blood flow are a valuable tool to investigate the pathophysiology of ascending thoratic aortic aneurysms (ATAA). To accurately reproduce in vivo hemodynamics, computational fluid dynamics (CFD) models must employ realistic inflow boundary conditions (BCs). However, the limited availability of in vivo velocity measurements, still makes researchers resort to idealized BCs. The aim of this study was to generate and thoroughly characterize a large dataset of synthetic 4D aortic velocity profiles sampled on a 2D cross-section along the ascending aorta with features similar to clinical cohorts of patients with ATAA. Time-resolved 3D phase contrast magnetic resonance (4D flow MRI) scans of 30 subjects with ATAA were processed through in-house code to extract anatomically consistent cross-sectional planes along the ascending aorta, ensuring spatial alignment among all planes and interpolating all velocity fields to a reference configuration. Velocity profiles of the clinical cohort were extensively characterized by computing flow morphology descriptors of both spatial and temporal features. By exploiting principal component analysis (PCA), a statistical shape model (SSM) of 4D aortic velocity profiles was built and a dataset of 437 synthetic cases with realistic properties was generated. Comparison between clinical and synthetic datasets showed that the synthetic data presented similar characteristics as the clinical population in terms of key morphological parameters. The average velocity profile qualitatively resembled a parabolic-shaped profile, but was quantitatively characterized by more complex flow patterns which an idealized profile would not replicate. Statistically significant correlations were found between PCA principal modes of variation and flow descriptors. We built a data-driven generative model of 4D aortic inlet velocity profiles, suitable to be used in computational studies of blood flow. The proposed software system also allows to map any of the generated velocity profiles to the inlet plane of any virtual subject given its coordinate set.

Sections du résumé

BACKGROUND AND OBJECTIVE OBJECTIVE
Numerical simulations of blood flow are a valuable tool to investigate the pathophysiology of ascending thoratic aortic aneurysms (ATAA). To accurately reproduce in vivo hemodynamics, computational fluid dynamics (CFD) models must employ realistic inflow boundary conditions (BCs). However, the limited availability of in vivo velocity measurements, still makes researchers resort to idealized BCs. The aim of this study was to generate and thoroughly characterize a large dataset of synthetic 4D aortic velocity profiles sampled on a 2D cross-section along the ascending aorta with features similar to clinical cohorts of patients with ATAA.
METHODS METHODS
Time-resolved 3D phase contrast magnetic resonance (4D flow MRI) scans of 30 subjects with ATAA were processed through in-house code to extract anatomically consistent cross-sectional planes along the ascending aorta, ensuring spatial alignment among all planes and interpolating all velocity fields to a reference configuration. Velocity profiles of the clinical cohort were extensively characterized by computing flow morphology descriptors of both spatial and temporal features. By exploiting principal component analysis (PCA), a statistical shape model (SSM) of 4D aortic velocity profiles was built and a dataset of 437 synthetic cases with realistic properties was generated.
RESULTS RESULTS
Comparison between clinical and synthetic datasets showed that the synthetic data presented similar characteristics as the clinical population in terms of key morphological parameters. The average velocity profile qualitatively resembled a parabolic-shaped profile, but was quantitatively characterized by more complex flow patterns which an idealized profile would not replicate. Statistically significant correlations were found between PCA principal modes of variation and flow descriptors.
CONCLUSIONS CONCLUSIONS
We built a data-driven generative model of 4D aortic inlet velocity profiles, suitable to be used in computational studies of blood flow. The proposed software system also allows to map any of the generated velocity profiles to the inlet plane of any virtual subject given its coordinate set.

Identifiants

pubmed: 36921465
pii: S0169-2607(23)00134-7
doi: 10.1016/j.cmpb.2023.107468
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

107468

Informations de copyright

Copyright © 2023 The Authors. Published by Elsevier B.V. All rights reserved.

Auteurs

Simone Saitta (S)

Department of Information, Electronics and Bioengineering, Politecnico di Milano, Milan, Italy.

Ludovica Maga (L)

Department of Information, Electronics and Bioengineering, Politecnico di Milano, Milan, Italy; Department of Chemical Engineering, Imperial College London, London, UK.

Chloe Armour (C)

Department of Chemical Engineering, Imperial College London, London, UK.

Emiliano Votta (E)

Department of Information, Electronics and Bioengineering, Politecnico di Milano, Milan, Italy.

Declan P O'Regan (DP)

MRC London Institute of Medical Sciences, Imperial College London, London, United Kingdom.

M Yousuf Salmasi (MY)

Department of Surgery and Cancer, Imperial College London, London, United Kingdom.

Thanos Athanasiou (T)

Department of Surgery and Cancer, Imperial College London, London, United Kingdom.

Jonathan W Weinsaft (JW)

Department of Medicine (Cardiology), Weill Cornell College, New York, NY, USA.

Xiao Yun Xu (XY)

Department of Chemical Engineering, Imperial College London, London, UK.

Selene Pirola (S)

Department of Chemical Engineering, Imperial College London, London, UK; Department of BioMechanical Engineering, 3mE Faculty, Delft University of Technology, Delft, Netherlands. Electronic address: s.pirola@tudelft.nl.

Alberto Redaelli (A)

Department of Information, Electronics and Bioengineering, Politecnico di Milano, Milan, Italy.

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Classifications MeSH