Why the study?
Ascending aorta aneurysm onset and progression are intertwined with adverse hemodynamics, motivating in vivo characterization of hemodynamic spatiotemporal complexity and organization in aortas with and without dilation.
Does 4D flow MRI combined with Complex Networks theory characterize hemodynamic heterogeneity differently in dilated versus non-dilated ascending aortas?
Does 4D flow MRI combined with Complex Networks theory characterize hemodynamic heterogeneity differently in dilated versus non-dilated ascending aortas?
Applying Complex Networks theory to 4D flow MRI data successfully quantifies hemodynamic spatiotemporal complexity, demonstrating that ascending aorta dilation disrupts forward flow correlation.
First complex network analysis of 4D flow MRI shows hemodynamic differences in dilated aortas; leaves open clinical utility.
Motivated by the evidence that the onset and progression of the aneurysm of the ascending aorta (AAo) is intertwined with an adverse hemodynamic environment, the present study characterized in vivo the hemodynamic spatiotemporal complexity and organization in human aortas, with and without dilated AAo, exploring the relations with clinically relevant hemodynamic and geometric parameters. The Complex Networks (CNs) theory was applied for the first time to 4D flow magnetic resonance imaging (MRI) velocity data of ten patients, five of them presenting with AAo dilation. The time-histories along the cardiac cycle of velocity-based quantities were used to build correlation-based CNs. The CNs approach succeeded in capturing large-scale coherent flow features, delimiting flow separation and recirculation regions. CNs metrics highlighted that an increasing AAo dilation (expressed in terms of the ratio between the maximum AAo and aortic root diameter) disrupts the correlation in forward flow reducing the correlation persistence length, while preserving the spatiotemporal homogeneity of secondary flows. The application of CNs to in vivo 4D MRI data holds promise for a mechanistic understanding of the spatiotemporal complexity and organization of aortic flows, opening possibilities for the integration of in vivo quantitative hemodynamic information into risk stratification and classification criteria.
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Calò et al. (2021) studied this question.
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