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Shared Latent Structures Between Imaging Features and Biomarkers in Early Stages of Alzheimer's Disease: A Predictive Study

机译:阿尔茨海默病早期成像特征与生物标志物之间的共同潜在结构:预测研究

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摘要

Magnetic resonance imaging (MRI) provides high resolution brain morphological information and is used as a biomarker in neurodegenerative diseases. Population studies of brain morphology often seek to identify pathological structural changes related to different diagnostic categories (e.g.: controls, mild cognitive impairment or dementia) which normally describe highly heterogeneous groups with a single categorical variable. Instead, multiple biomarkers are used as a proxy for pathology and are more powerful in capturing structural variability. Hence, using the joint modeling of brain morphology and biomarkers, we aim at describing structural changes related to any brain condition by means of few underlying processes. In this regard, we use a multivariate approach based on Projection to Latent Structures in its regression variant (PLSR) to study structural changes related to aging and AD pathology. MRI volumetric and cortical thickness measurements are used for brain morphology and cerebrospinal fluid (CSF) biomarkers (t-tau, p-tau and amyloid-beta) are used as a proxy for AD pathology. By relating both sets of measurements, PLSR finds a low-dimensional latent space describing AD pathological effects on brain structure. The proposed framework allows us to separately model aging effects on brain morphology as a confounder variable orthogonal to the pathological effect. The predictive power of the associated latent spaces (i.e., the capacity of predicting biomarker values) is assessed in a cross-validation framework.
机译:磁共振成像(MRI)提供高分辨率脑形态信息,并用作神经变性疾病中的生物标志物。脑形态学的人口研究经常寻求鉴定与不同诊断类别(例如控制,轻度认知障碍或痴呆)相关的病理结构变化,其通常用单一的单一分类变量描述高度异质的组。相反,多个生物标志物用作病理学的代理,并且在捕获结构变异性方面更强大。因此,使用脑形态和生物标志物的联合建模,我们的目标是通过少数潜在的过程描述与任何脑状况相关的结构变化。在这方面,我们使用基于投影的多变量方法对其回归变量(PLSR)的潜在结构来研究与老化和广告病理相关的结构变化。 MRI体积和皮质厚度测量用于脑形态和脑脊髓液(CSF)生物标志物(T-TAU,P-TAU和淀粉样蛋白-β)用作AD病理学的代理。通过对两组测量相结合,PLSR发现了描述对脑结构上的广告病理影响的低维潜空间。所提出的框架使我们能够将老化对脑形态的衰老作用分别作为与病理效应正交的混淆变量。在交叉验证框架中评估相关潜在空间的预测力(即,预测生物标志物值的容量)。

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