发现弥散:人类心肌组织的自动模型发现有多鲁棒?

IF 2.7 3区 医学 Q2 BIOPHYSICS
Denisa Martonová, Sigrid Leyendecker, Gerhard A Holzapfel, Ellen Kuhl
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引用次数: 0

摘要

计算建模已经成为理解包括人类心肌在内的广泛生物组织结构组织和功能行为之间相互作用的不可或缺的工具。传统的本构模型,以及最近由自动模型发现生成的模型,通常基于完美排列纤维族的简化假设。然而,实验证据表明,许多纤维增强组织表现出局部分散,这可以显著影响其力学行为。在这里,我们将广义结构张量方法集成到自动材料模型发现中,通过使用方向的概率描述来表示围绕三个平均正交方向(纤维、薄片和法向)以旋转对称分布的纤维。利用人类心肌的双轴拉伸和三轴剪切数据,我们系统地改变了方向分散的程度和应力测量噪声,以探索所发现模型的鲁棒性。我们的研究结果表明,纤维方向上的中等色散以及薄片和法向方向上的任意色散提高了拟合的良好度,并使先前提出的四项模型能够恢复各向同性第二不变量,两个分散的各向异性不变量和一个耦合不变量。我们的方法具有很强的鲁棒性,即使在应力数据中存在高达7%的随机噪声的情况下,也能始终识别出相似的模型项。总之,我们的研究表明,基于强大的广义结构张量的自动模型发现对噪声具有鲁棒性,并以生理上有意义的方式捕获微观结构的不确定性和异质性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Discovering dispersion: How robust is automated model discovery for human myocardial tissue?

Computational modeling has become an integral tool for understanding the interaction between structural organization and functional behavior in a wide range of biological tissues, including the human myocardium. Traditional constitutive models, and recent models generated by automated model discovery, are often based on the simplifying assumption of perfectly aligned fiber families. However, experimental evidence suggests that many fiber-reinforced tissues exhibit local dispersion, which can significantly influence their mechanical behavior. Here, we integrate the generalized structure tensor approach into automated material model discovery to represent fibers that are distributed with rotational symmetry around three mean orthogonal directions-fiber, sheet, and normal-by using probabilistic descriptions of the orientation. Using biaxial extension and triaxial shear data from human myocardium, we systematically vary the degree of directional dispersion and stress measurement noise to explore the robustness of the discovered models. Our findings reveal that up to a moderate dispersion in the fiber direction and arbitrary dispersion in the sheet and normal directions improve the goodness of fit and enable recovery of a previously proposed four-term model in terms of the isotropic second invariant, two dispersed anisotropic invariants, and one coupling invariant. Our approach demonstrates strong robustness and consistently identifies similar model terms, even in the presence of up to 7% random noise in the stress data. In summary, our study suggests that automated model discovery based on the powerful generalized structure tensors is robust to noise and captures microstructural uncertainty and heterogeneity in a physiologically meaningful way.

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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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