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Alzheimer's Disease Modelling and Staging Through Independent Gaussian Process Analysis of Spatio-Temporal Brain Changes

机译:阿尔茨海默氏病的建模和分期,通过时空脑部变化的独立高斯过程分析

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Alzheimer's disease (AD) is characterized by complex and largely unknown progression dynamics affecting the brain's morphology. Although the disease evolution spans decades, to date we cannot rely on long-term data to model the pathological progression, since most of the available measures are on a short-term scale. It is therefore difficult to understand and quantify the temporal progression patterns affecting the brain regions across the AD evolution. In this work, we present a generative model based on probabilistic matrix factorization across temporal and spatial sources. The proposed method addresses the problem of disease progression modelling by introducing clinically-inspired statistical priors. To promote smoothness in time and model plausible pathological evolutions, the temporal sources are defined as monotonic and independent Gaussian Processes. We also estimate an individual time-shift parameter for each patient to automatically position him/her along the sources time-axis. To encode the spatial continuity of the brain substructures, the spatial sources are modeled as Gaussian random fields. We test our algorithm on grey matter maps extracted from brain structural images. The experiments highlight differential temporal progression patterns mapping brain regions key to the AD pathology, and reveal a disease-specific time scale associated with the decline of volumetric biomarkers across clinical stages.
机译:阿尔茨海默氏病(AD)的特征是复杂且很大程度上未知的影响大脑形态的进展动态。尽管疾病的发展跨越了几十年,但迄今为止,我们无法依靠长期数据来模拟病理进展,因为大多数可用的措施都是短期的。因此,难以理解和量化影响整个AD进化过程中影响大脑区域的时间进展模式。在这项工作中,我们提出了一种基于跨时空源的概率矩阵分解的生成模型。所提出的方法通过引入临床启发性的统计先验来解决疾病进展建模的问题。为了促进时间的平滑并模拟可能的病理演变,将时间源定义为单调且独立的高斯过程。我们还为每个患者估计一个单独的时移参数,以沿源时间轴自动定位他/她。为了编码大脑子结构的空间连续性,将空间源建模为高斯随机场。我们在从大脑结构图像提取的灰质图上测试我们的算法。实验强调了不同的时间进展模式,该模式绘制了AD病理关键区域的大脑区域,并揭示了特定疾病的时间尺度,该尺度与整个临床阶段的容量生物标志物的下降有关。

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