Brain Shape Changes Associated With Cerebral Atrophy in Healthy Aging and Alzheimer’s Disease

IF 2 Q2 ENGINEERING, MECHANICAL Frontiers in Mechanical Engineering Pub Date : 2021-07-01 DOI:10.3389/fmech.2021.705653
Yana Blinkouskaya, J. Weickenmeier
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引用次数: 20

Abstract

Both healthy and pathological brain aging are characterized by various degrees of cognitive decline that strongly correlate with morphological changes referred to as cerebral atrophy. These hallmark morphological changes include cortical thinning, white and gray matter volume loss, ventricular enlargement, and loss of gyrification all caused by a myriad of subcellular and cellular aging processes. While the biology of brain aging has been investigated extensively, the mechanics of brain aging remains vastly understudied. Here, we propose a multiphysics model that couples tissue atrophy and Alzheimer’s disease biomarker progression. We adopt the multiplicative split of the deformation gradient into a shrinking and an elastic part. We model atrophy as region-specific isotropic shrinking and differentiate between a constant, tissue-dependent atrophy rate in healthy aging, and an atrophy rate in Alzheimer’s disease that is proportional to the local biomarker concentration. Our finite element modeling approach delivers a computational framework to systematically study the spatiotemporal progression of cerebral atrophy and its regional effect on brain shape. We verify our results via comparison with cross-sectional medical imaging studies that reveal persistent age-related atrophy patterns. Our long-term goal is to develop a diagnostic tool able to differentiate between healthy and accelerated aging, typically observed in Alzheimer’s disease and related dementias, in order to allow for earlier and more effective interventions.
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健康老龄化和阿尔茨海默病中脑形状变化与脑萎缩相关
无论是健康的还是病理性的大脑衰老,其特征都是不同程度的认知能力下降,这与被称为脑萎缩的形态变化密切相关。这些标志性的形态学改变包括皮层变薄、白质和灰质体积减少、心室增大和回转体丧失,所有这些都是由无数的亚细胞和细胞衰老过程引起的。虽然大脑衰老的生物学已被广泛研究,但大脑衰老的机制仍未得到充分研究。在这里,我们提出了一个多物理场模型,结合组织萎缩和阿尔茨海默病的生物标志物进展。我们将变形梯度相乘分割为收缩部分和弹性部分。我们将萎缩建模为特定区域的各向同性萎缩,并区分健康衰老中恒定的、组织依赖的萎缩率和阿尔茨海默病中与局部生物标志物浓度成正比的萎缩率。我们的有限元建模方法提供了一个计算框架来系统地研究脑萎缩的时空进展及其对脑形状的区域影响。我们通过与横断面医学成像研究的比较来验证我们的结果,这些研究揭示了持续的与年龄相关的萎缩模式。我们的长期目标是开发一种诊断工具,能够区分健康衰老和加速衰老(通常在阿尔茨海默病和相关痴呆症中观察到),以便进行更早、更有效的干预。
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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来源期刊
Frontiers in Mechanical Engineering
Frontiers in Mechanical Engineering Engineering-Industrial and Manufacturing Engineering
CiteScore
4.40
自引率
0.00%
发文量
115
审稿时长
14 weeks
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