Exploring tau protein and amyloid-beta propagation: a sensitivity analysis of mathematical models based on biological data.

ArXiv Pub Date : 2024-09-04
Mattia Corti
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Abstract

Alzheimer's disease is the most common dementia worldwide. Its pathological development is well known to be connected with the accumulation of two toxic proteins: tau protein and amyloid-$\beta$. Mathematical models and numerical simulations can predict the spreading patterns of misfolded proteins in this context. However, the calibration of the model parameters plays a crucial role in the final solution. In this work, we perform a sensitivity analysis of heterodimer and Fisher-Kolmogorov models to evaluate the impact of the equilibrium values of protein concentration on the solution patterns. We adopt advanced numerical methods such as the IMEX-DG method to accurately describe the propagating fronts in the propagation phenomena in a polygonal mesh of sagittal patient-specific brain geometry derived from magnetic resonance images. We calibrate the model parameters using biological measurements in the brain cortex for the tau protein and the amyloid-$\beta$ in Alzheimer's patients and controls. Finally, using the sensitivity analysis results, we discuss the applicability of both models in the correct simulation of the spreading of the two proteins.

探索 tau 蛋白和淀粉样蛋白-β 的传播:基于生物数据的数学模型敏感性分析。
阿尔茨海默病是全球最常见的痴呆症。众所周知,其病理发展与两种有毒蛋白质的积累有关:tau 蛋白和淀粉样蛋白。在这种情况下,数学模型和数值模拟可以预测错误折叠蛋白的扩散模式。然而,模型参数的校准对最终解决方案起着至关重要的作用。在这项工作中,我们对异源二聚体模型和 Fisher-Kolmogorov 模型进行了敏感性分析,以评估蛋白质浓度平衡值对溶液模式的影响。我们采用先进的数值方法(如 IMEX-DG 方法),在根据磁共振图像得出的矢状患者特定脑几何形状的多边形网格中精确描述传播现象中的传播前沿。我们利用大脑皮层对阿尔茨海默氏症患者和对照组的 tau 蛋白和淀粉样蛋白-$/beta$的生物测量结果校准模型参数。最后,利用敏感性分析结果,我们讨论了这两种模型在正确模拟两种蛋白质扩散方面的适用性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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