Fractal Dimension Analyses to Detect Alzheimer’s and Parkinson’s Diseases Using Their Thin Brain Tissue Samples via Transmission Optical Microscopy

Ishmael Apachigawo, Dhruvil Solanki, Ruth Tate, Himanshi Singh, Mohammad Moshahid Khan, Prabhakar Pradhan
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Abstract

Biological tissues in nature are fractal due to their self-similarity and porosity properties. These properties change with the progress of some diseases, including brain tissue in leading neurological disorders such as Alzheimer’s disease (AD) and Parkinson’s disease (PD). Thus, there is an unmet clinical need to develop a tool for accurate and early diagnosis of AD and PD conditions. Although the whole brain tissues in AD and PD have been extensively studied, their local structural alterations at the nano-to-submicron levels have not been explored. In this paper, we measure the local structural alterations in different brain regions of AD and PD patients by measuring their change in fractal dimensions via optical microscopy. Our results show an increase in the fractal dimension value of ~5–10% in the affected regions of the brain tissues relative to their respective controls. For AD cases, the structural alteration is attributed to the aberrant deposition of amyloid beta protein and neurofibrillary tangles in the brain, and for PD, the gradual loss of dopaminergic neurons and abnormal accumulation of α-synuclein in the brain. The work will enhance the further understanding of alterations in the brain structures in AD and PD and its detection.
分形维数分析通过透射光学显微镜检测阿尔茨海默病和帕金森病的薄脑组织样本
自然界的生物组织由于具有自相似性和多孔性而具有分形特征。这些特性随着一些疾病的进展而改变,包括阿尔茨海默病(AD)和帕金森病(PD)等主要神经系统疾病的脑组织。因此,开发一种准确、早期诊断AD和PD的工具是尚未满足的临床需求。尽管人们对AD和PD的整个脑组织进行了广泛的研究,但它们在纳米到亚微米水平上的局部结构改变尚未被探索。本文通过光学显微镜测量AD和PD患者的分形维数变化,来测量AD和PD患者大脑不同区域的局部结构改变。我们的研究结果显示,与各自的对照相比,脑组织受影响区域的分形维值增加了~ 5-10%。对于AD病例,结构改变归因于大脑中淀粉样蛋白和神经原纤维缠结的异常沉积,对于PD,多巴胺能神经元的逐渐丧失和α-突触核蛋白的异常积累。这项工作将有助于进一步了解阿尔茨海默病和帕金森病的大脑结构变化及其检测。
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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