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Cross-View Neuroimage Pattern Analysis in Alzheimers Disease Staging

机译:阿尔茨海默氏病分期的跨视野神经图像模式分析

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摘要

The research on staging of pre-symptomatic and prodromal phase of neurological disorders, e.g., Alzheimer's disease (AD), is essential for prevention of dementia. New strategies for AD staging with a focus on early detection, are demanded to optimize potential efficacy of disease-modifying therapies that can halt or slow the disease progression. Recently, neuroimaging are increasingly used as additional research-based markers to detect AD onset and predict conversion of MCI and normal control (NC) to AD. Researchers have proposed a variety of neuroimaging biomarkers to characterize the patterns of the pathology of AD and MCI, and suggested that multi-view neuroimaging biomarkers could lead to better performance than single-view biomarkers in AD staging. However, it is still unclear what leads to such synergy and how to preserve or maximize. In an attempt to answer these questions, we proposed a cross-view pattern analysis framework for investigating the synergy between different neuroimaging biomarkers. We quantitatively analyzed nine types of biomarkers derived from FDG-PET and T1-MRI, and evaluated their performance in a task of classifying AD, MCI, and NC subjects obtained from the ADNI baseline cohort. The experiment results showed that these biomarkers could depict the pathology of AD from different perspectives, and output distinct patterns that are significantly associated with the disease progression. Most importantly, we found that these features could be separated into clusters, each depicting a particular aspect; and the inter-cluster features could always achieve better performance than the intra-cluster features in AD staging.
机译:对神经系统疾病如阿尔茨海默氏病(AD)的症状前期和前驱期阶段进行研究对于预防痴呆至关重要。需要以早期发现为重点的新的AD分期策略,以优化可中止或减慢疾病进展的疾病改良疗法的潜在功效。最近,神经影像越来越多地用作基于研究的其他标记,以检测AD发作并预测MCI和正常对照(NC)向AD的转化。研究人员已经提出了多种神经影像生物标记物来表征AD和MCI的病理模式,并建议在AD分期中,多视野神经影像生物标记物可以比单视野生物标记物产生更好的性能。但是,仍不清楚是什么导致了这种协同作用以及如何保持或最大化。为了回答这些问题,我们提出了一种跨视图模式分析框架,用于研究不同神经成像生物标记之间的协同作用。我们定量分析了源自FDG-PET和T1-MRI的9种类型的生物标志物,并评估了它们在分类从ADNI基线队列获得的AD,MCI和NC受试者中的表现。实验结果表明,这些生物标记物可以从不同角度描述AD的病理,并输出与疾病进展显着相关的独特模式。最重要的是,我们发现这些功能可以分为多个群集,每个群集描绘一个特定方面。并且群集间功能始终可以比AD过渡中的群集内功能始终获得更好的性能。

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