利用磁共振成像深度编码器-解码器网络,通过机器学习和 ADmod:时空感知脑淀粉样蛋白β生长模型,对阿尔茨海默病进行定量分析,并利用磁共振成像数据构建早期阿尔茨海默病检测深度学习系统 (EADDLS)

Naitik Mohanty, Morteza Sarmadi
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引用次数: 0

摘要

阿尔茨海默病(AD)是一项重大的社会挑战,目前尚无治愈方法,而且在老年人中的发病率越来越高。本研究将机器学习的潜力应用于纵向核磁共振成像数据,以满足早期检测的迫切需要。数据集来自 "开放存取系列成像研究(OASIS)"项目,包括 150 名 60 至 96 岁受试者的磁共振成像记录,每位受试者至少接受过一次扫描。值得注意的是,72 名受试者被归类为 "非痴呆",64 名受试者被归类为 "痴呆",14 名受试者经历了从 "非痴呆 "到 "痴呆 "的转变,形成了 "转换 "类别。我们的建议是,利用从核磁共振成像数据中提取的关键生物标志物,开发一种能够预测轻度认知障碍进展的机器学习健全模型。所选的生物标志物包括教育年限(EDUC)、社会经济地位(SES)、迷你精神状态检查(MMSE)、临床痴呆评级(CDR)、估计颅内总容积(eTIV)、归一化全脑容积(nWBV)和阿特拉斯缩放因子(ASF)。本研究参考了该领域之前的工作,重点介绍了主要侧重于原始 MRI 数据分析的研究。相比之下,本研究引入了一种独特的方法,即利用一组经过筛选的生物标志物,建立一个更有针对性、更有可能解释的模型。本研究采用了逻辑回归、支持向量机、决策树、随机森林分类器和 AdaBoost 等机器学习模型,并使用既定指标来衡量性能。有关严重程度和状态的信息在 EADDLS 模块中存储,并用于 ADmod。ADmod 使用 EADDLS 模块中存储的核磁共振成像数据,利用卷积法对大脑中淀粉样蛋白 β 的堆积增长进行建模,从而得出通用方法和针对特定患者的方法。使用偏微分方程(或 PDEs)建立淀粉样β堆积模型的数学实例很多,但由于运行时间延长、存储限制以及预设条件的限制,这些模型仍未被纳入。我们提出了一种新型淀粉样蛋白β生长模型,该模型使用深度编码器-解码器网络和卷积技术。这项研究为早期阿尔茨海默氏症检测领域日益增多的研究做出了贡献,提供了见解、结果并讨论了局限性。结论概述了一种独特的方法,强调了拟议模型的实际应用,承认了局限性,并提出了进一步研究的途径。早期发现注意力缺失症可以大大提高患者的护理质量,并有助于未来采取预防或风险评估措施。
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A quantitative analysis of Alzheimers Disease and construction of an early Alzheimers detection deep learning system (EADDLS) using MRI data via machine learning along with ADmod: spatiotemporal-aware brain-amyloidβ growth model, using deep encoder-decoder networks about MRI
Alzheimer's disease (AD) presents a significant societal challenge, with no current cure and an increasing prevalence among older adults. This study addresses the pressing need for early detection by harnessing the potential of machine learning applied to longitudinal MRI data. The dataset, sourced from the Open Access Series of Imaging Studies (OASIS) project, comprises MRI records of 150 subjects aged 60 to 96, each scanned at least once. Notably, 72 subjects were classified as 'Nondemented,' 64 as 'Demented,' and 14 underwent a transition from 'Nondemented' to 'Demented,' forming the 'Converted' category. What we propose is to develop a machine learning sound model capable of predicting the progression of mild cognitive impairment, leveraging key biomarkers extracted from MRI data. The chosen biomarkers include years of education (EDUC), socioeconomic status (SES), Mini-Mental State Examination (MMSE), Clinical Dementia Rating (CDR), Estimated Total Intracranial Volume (eTIV), Normalized Whole Brain Volume (nWBV), and Atlas Scaling Factor (ASF). Prior work in the field is referenced, highlighting studies that predominantly focused on raw MRI data analysis. In contrast, this study introduces a unique approach by utilizing a curated set of biomarkers, allowing for a more targeted and potentially interpretable model. Machine learning models such as Logistic Regression, Support Vector Machine, Decision Tree, Random Forest Classifier, and AdaBoost are employed, with performance measured using established metrics. Information about severity and state are stored during the EADDLS module and used for ADmod. ADmod uses the stored MRI data during the EADDLS module to model the growth of amyloid β build-up in the brain using convolution, resulting in both generalizable approaches and patient-specific approaches. There have been numerous mathematical instantiations to model amyloid β build-up using partial differential equations (or PDEs), these however have remained unincorporated due to prolonged runtimes and storage limitations along with those of pre-set conditions. We propose a novel amyloid β growth model using deep encoder-decoder networks in conjunction with convolution. The study contributes to the growing body of research in early Alzheimer's detection, offering insights, results, and a discussion of limitations. The conclusion outlines a unique approach, emphasizes the practical implementation of the proposed model, acknowledges limitations, and suggests avenues for further research. Early detection of AD can significantly better the patient's quality of care and lead to future preventative or risk assessment measures.
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