TY - JOUR
T1 - A multi-modal computational fluid dynamics model of left atrial fibrillation haemodynamics validated with 4D flow MRI
AU - Parker, Louis
AU - Bollache, Emilie
AU - Soulez, Shannon
AU - Bouazizi, Khaoula
AU - Badenco, Nicolas
AU - Giese, Daniel
AU - Gandjbakhch, Estelle
AU - Redheuil, Alban
AU - Laredo, Mikael
AU - Kachenoura, Nadjia
N1 - Publisher Copyright:
© The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature 2025.
PY - 2025/2
Y1 - 2025/2
N2 - Atrial fibrillation (AF) is characterized by rapid and irregular contraction of the left atrium (LA). Impacting LA haemodynamics, this increases the risk of thrombi development and stroke. Flow conditions preceding stroke in these patients are not well defined, partly due the limited resolution of 4D flow magnetic resonance imaging (MRI). In this study, we combine a high-resolution computed tomography (CT) LA reconstruction with motion and pulmonary inflows from 4D flow MRI to create a novel multimodal computational fluid dynamics (CFD) model, applying it to five AF patients imaged in sinus rhythm (24 ± 39 days between acquisitions). The dynamic model was compared with a rigid wall equivalent and the main flow structures were validated with 4D flow MRI. Point-by-point absolute differences between the velocity fields showed moderate differences given the sensitivity to registration. The rigid wall model significantly underestimated LA time-averaged wall shear stress (TAWSS) (p = 0.02) and oscillatory shear index (OSI) (p = 0.02) compared to the morphing model. Similarly, in the left atrial appendage (LAA), TAWSS (p = 0.003) and OSI (p < 0.001) were further underestimated. The morphing model yielded a more accurate mitral valve waveform and showed low TAWSS and high OSI in the LAA, both associated with thrombus formation. We also observed a positive correlation between indexed LA volume and endothelial cell activation potential (ECAP) (R2 = 0.83), as well as LAA volume and LAA OSI (R2 = 0.70). This work demonstrates the importance of LA motion in modelling LAA flow. Assessed in larger cohorts, LAA haemodynamic analysis may be beneficial to refine stroke risk assessment for AF.
AB - Atrial fibrillation (AF) is characterized by rapid and irregular contraction of the left atrium (LA). Impacting LA haemodynamics, this increases the risk of thrombi development and stroke. Flow conditions preceding stroke in these patients are not well defined, partly due the limited resolution of 4D flow magnetic resonance imaging (MRI). In this study, we combine a high-resolution computed tomography (CT) LA reconstruction with motion and pulmonary inflows from 4D flow MRI to create a novel multimodal computational fluid dynamics (CFD) model, applying it to five AF patients imaged in sinus rhythm (24 ± 39 days between acquisitions). The dynamic model was compared with a rigid wall equivalent and the main flow structures were validated with 4D flow MRI. Point-by-point absolute differences between the velocity fields showed moderate differences given the sensitivity to registration. The rigid wall model significantly underestimated LA time-averaged wall shear stress (TAWSS) (p = 0.02) and oscillatory shear index (OSI) (p = 0.02) compared to the morphing model. Similarly, in the left atrial appendage (LAA), TAWSS (p = 0.003) and OSI (p < 0.001) were further underestimated. The morphing model yielded a more accurate mitral valve waveform and showed low TAWSS and high OSI in the LAA, both associated with thrombus formation. We also observed a positive correlation between indexed LA volume and endothelial cell activation potential (ECAP) (R2 = 0.83), as well as LAA volume and LAA OSI (R2 = 0.70). This work demonstrates the importance of LA motion in modelling LAA flow. Assessed in larger cohorts, LAA haemodynamic analysis may be beneficial to refine stroke risk assessment for AF.
KW - Atrial fibrillation
KW - Computational fluid dynamics
KW - Fluid mechanics
KW - Hemodynamics
KW - Multi-modal
UR - https://www.scopus.com/pages/publications/85217422739
U2 - 10.1007/s10237-024-01901-y
DO - 10.1007/s10237-024-01901-y
M3 - Article
C2 - 39828784
AN - SCOPUS:85217422739
SN - 1617-7959
VL - 24
SP - 139
EP - 152
JO - Biomechanics and Modeling in Mechanobiology
JF - Biomechanics and Modeling in Mechanobiology
IS - 1
ER -