A combined 4D flow MR imaging and fluid-structure interaction analysis of ascending thoracic aortic aneurysms.

IF 3 3区 医学 Q2 BIOPHYSICS
Yu Zhu, Chlöe Armour, Binghuan Li, Selene Pirola, Yousuf Salmasi, Thanos Athanasiou, Declan P O'Regan, Xiao Yun Xu
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引用次数: 0

Abstract

This study aimed to characterize the altered hemodynamics and wall mechanics in ascending thoracic aortic aneurysms (ATAA) by employing fully coupled two-way fluid-structure interaction (FSI) analyses. Our FSI models incorporated hyperelastic wall mechanical properties, prestress, and patient-specific inlet velocity profiles (IVP) extracted from 4D flow magnetic resonance imaging (MRI). By performing FSI analyses on 7 patient-specific ATAA models and 6 healthy aortas, the primary objective of the study was to compare hemodynamic and biomechanical features in ATAA versus healthy controls. A secondary objective was to examine the need for 4D flow MRI-derived IVP in FSI simulations by comparing results with those using two commonly adopted idealized IVPs: Flat-IVP and Para-IVP for selected cases. Our results show that, compared to the healthy aortas, the ATAA models exhibited highly disturbed blood flow in the ascending aorta. Consequently, maximum turbulent kinetic energy (TKE) at peak systole (155.0 ± 188.4 Pa) and maximum time-averaged wall shear stress (TAWSS) (8.6 ± 6.5 Pa) were significantly higher in the ATAA cohort, compared to 0.6 ± 0.5 Pa and 2.8 ± 0.7 Pa in the healthy aortas. Peak wall stress was also nearly doubled in the ATAA group (414 ± 108 kPa vs. 215 ± 31 kPa). Additionally, comparisons of simulation results across models with different IVPs underscore the importance of prescribing 3D-IVP at the inlet, especially for ATAA cases. Using idealized IVPs in two selected ATAA models (P1 and P7) substantially reduced the maximum TKE from 571 Pa to 0.01 Pa (Flat-IVP) and 0.02 Pa (Para-IVP) in P1 and from 73 Pa to 0.01 Pa (Flat-IVP) and 0.08 Pa (Para-IVP) in P7, while the maximum TAWSS in the ascending aorta decreased from 9.6 Pa to 0.7 Pa (Flat-IVP) and 0.9 Pa (Para-IVP) in P1, and from 3.6 Pa to 1.2 Pa and 0.9 Pa, respectively, in P7. Moreover, idealized IVPs also caused the peak wall stress to reduce by up to 11.5% in P1 with severe aortic valve stenosis, and by up to 2% in P7 with mild aortic regurgitation. These results highlight the importance of FSI simulations combined with 4D flow MRI in capturing realistic hemodynamic and biomechanical changes in aneurysmal aortas.

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来源期刊
Biomechanics and Modeling in Mechanobiology
Biomechanics and Modeling in Mechanobiology 工程技术-工程:生物医学
CiteScore
7.10
自引率
8.60%
发文量
119
审稿时长
6 months
期刊介绍: Mechanics regulates biological processes at the molecular, cellular, tissue, organ, and organism levels. A goal of this journal is to promote basic and applied research that integrates the expanding knowledge-bases in the allied fields of biomechanics and mechanobiology. Approaches may be experimental, theoretical, or computational; they may address phenomena at the nano, micro, or macrolevels. Of particular interest are investigations that (1) quantify the mechanical environment in which cells and matrix function in health, disease, or injury, (2) identify and quantify mechanosensitive responses and their mechanisms, (3) detail inter-relations between mechanics and biological processes such as growth, remodeling, adaptation, and repair, and (4) report discoveries that advance therapeutic and diagnostic procedures. Especially encouraged are analytical and computational models based on solid mechanics, fluid mechanics, or thermomechanics, and their interactions; also encouraged are reports of new experimental methods that expand measurement capabilities and new mathematical methods that facilitate analysis.
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