冠状动脉患者特异性介观流体-结构相互作用模型

IF 2.2 4区 医学 Q3 ENGINEERING, BIOMEDICAL
Elisabeth Steadman, Daphne Meza, David A. Rubenstein, Wei Yin
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引用次数: 0

摘要

利用COMSOL Multiphysics开发了一个聚焦于左冠状动脉小感兴趣区域(ROI)的介观流固耦合(FSI)模型。该模型是在先前建立的患者特异性冠状动脉宏观FSI模型的基础上建立的。由于元素大小与内皮细胞相当,介观模型的空间分辨率得到了显著提高。计算正常和狭窄(50%和71%闭塞)冠状动脉roi中血流引起的剪切应力及其衍生物、血管壁Mises应力和拉应变(径向和周向),并将目前的细观模型与先前建立的宏观模型进行比较。50%狭窄模型的剪切应力和周向应变有显著差异。利用剪切-拉伸装置将介观狭窄模型衍生的剪切应力和拉伸应变同时施加于人冠状动脉内皮细胞,并测量内皮细胞的反应(细胞形态和细胞表面ICAM-1表达)。结果表明,从细观FSI模型和先前开发的宏观模型计算的剪切应力-拉伸应变条件的差异对内皮细胞反应有显著影响,这表明大规模的FSI模型可能不足以表征细胞水平的局部生物力学条件。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

A Patient-Specific Mesoscopic Fluid–Structure Interaction Model of the Coronary Artery

A Patient-Specific Mesoscopic Fluid–Structure Interaction Model of the Coronary Artery

A mesoscopic fluid–structure interaction (FSI) model focusing on a small region of interest (ROI) in the left coronary artery was developed using COMSOL Multiphysics. This model was on the basis of a previously developed patient-specific coronary artery macroscopic FSI model. With element size comparable to that of endothelial cells, the spatial resolution of the mesoscopic model was significantly improved. Blood flow-induced shear stress and derivatives, vascular wall von Mises stress, and tensile strain (radial and circumferential) in normal and stenosed (50% and 71% occlusion) coronary artery ROIs were calculated, and the results were compared between the current mesoscopic model and the previously developed macroscopic model. Significant differences were observed in shear stress and circumferential strain in the 50% stenosis models. The mesoscopic stenosis model-derived shear stress and tensile strain were applied to human coronary artery endothelial cells concurrently using a shearing-stretching device, and endothelial cell responses (cell morphology and cell surface ICAM-1 expression) were measured. The results demonstrated that the difference in shear stress–tensile strain conditions calculated from the mesoscopic FSI model and the previously developed macroscopic model had a significant impact on endothelial cell responses, suggesting that large-scale FSI models may not be sufficient to characterize local biomechanical conditions at the cellular level.

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来源期刊
International Journal for Numerical Methods in Biomedical Engineering
International Journal for Numerical Methods in Biomedical Engineering ENGINEERING, BIOMEDICAL-MATHEMATICAL & COMPUTATIONAL BIOLOGY
CiteScore
4.50
自引率
9.50%
发文量
103
审稿时长
3 months
期刊介绍: All differential equation based models for biomedical applications and their novel solutions (using either established numerical methods such as finite difference, finite element and finite volume methods or new numerical methods) are within the scope of this journal. Manuscripts with experimental and analytical themes are also welcome if a component of the paper deals with numerical methods. Special cases that may not involve differential equations such as image processing, meshing and artificial intelligence are within the scope. Any research that is broadly linked to the wellbeing of the human body, either directly or indirectly, is also within the scope of this journal.
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