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Growth Description for Vessel Wall Adaptation: A Thick-Walled Mixture Model of Abdominal Aortic Aneurysm Evolution

机译:血管壁适应的生长描述:腹主动脉瘤演变的厚壁混合物模型。

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摘要

(1) Background: Vascular tissue seems to adapt towards stable homeostatic mechanical conditions, however, failure of reaching homeostasis may result in pathologies. Current vascular tissue adaptation models use many ad hoc assumptions, the implications of which are far from being fully understood; (2) Methods: The present study investigates the plausibility of different growth kinematics in modeling Abdominal Aortic Aneurysm (AAA) evolution in time. A structurally motivated constitutive description for the vessel wall is coupled to multi-constituent tissue growth descriptions; Constituent deposition preserved either the constituent’s density or its volume, and Isotropic Volume Growth (IVG), in-Plane Volume Growth (PVG), in-Thickness Volume Growth (TVG) and No Volume Growth (NVG) describe the kinematics of the growing vessel wall. The sensitivity of key modeling parameters is explored, and predictions are assessed for their plausibility; (3) Results: AAA development based on TVG and NVG kinematics provided not only quantitatively, but also qualitatively different results compared to IVG and PVG kinematics. Specifically, for IVG and PVG kinematics, increasing collagen mass production accelerated AAA expansion which seems counterintuitive. In addition, TVG and NVG kinematics showed less sensitivity to the initial constituent volume fractions, than predictions based on IVG and PVG; (4) Conclusions: The choice of tissue growth kinematics is of crucial importance when modeling AAA growth. Much more interdisciplinary experimental work is required to develop and validate vascular tissue adaption models, before such models can be of any practical use.
机译:(1)背景:血管组织似乎适应稳定的稳态机械状态,但是,达到稳态的失败可能导致病理。当前的血管组织适应模型使用许多特殊的假设,其含义远未得到充分理解。 (2)方法:本研究调查了不同生长运动学在及时模拟腹主动脉瘤(AAA)演变中的合理性。血管壁的结构性本构描述与多组织组织生长描述结合;成分沉积保留了成分的密度或其体积,各向同性的体积增长(IVG),平面内的体积增长(PVG),厚度内的体积增长(TVG)和无体积增长(NVG)描述了生长血管的运动学壁。探索关键建模参数的敏感性,并评估其合理性的预测; (3)结果:与IVG和PVG运动学相比,基于TVG和NVG运动学的AAA开发不仅提供了定量的结果,而且在质量上也提供了不同的结果。具体而言,对于IVG和PVG运动学,增加胶原蛋白的大量生产会加速AAA的扩展,这似乎是违反直觉的。此外,与基于IVG和PVG的预测相比,TVG和NVG运动学对初始成分体积分数的敏感性更低。 (4)结论:在模拟AAA生长时,组织生长运动学的选择至关重要。在开发和验证血管组织适应性模型之前,还需要进行更多的跨学科实验工作,才能使此类模型具有任何实际用途。

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