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Clustering Analysis of FDG-PET Imaging in Primary Progressive Aphasia

机译:FDG-PET显像在原发性进行性失语症中的聚类分析

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摘要

>Background: Primary progressive aphasia (PPA) is a clinical syndrome characterized by the neurodegeneration of language brain systems. Three main clinical forms (non-fluent, semantic, and logopenic PPA) have been recognized, but applicability of the classification and the capacity to predict the underlying pathology is controversial. We aimed to study FDG-PET imaging data in a large consecutive case series of patients with PPA to cluster them into different subtypes according to regional brain metabolism.>Methods: 122 FDG-PET imaging studies belonging to 91 PPA patients and 28 healthy controls were included. We developed a hierarchical agglomerative cluster analysis with Ward's linkage method, an unsupervised clustering algorithm. We conducted voxel-based brain mapping analysis to evaluate the patterns of hypometabolism of each identified cluster.>Results: Cluster analysis confirmed the three current PPA variants, but the optimal number of clusters according to Davies-Bouldin index was 6 subtypes of PPA. This classification resulted from splitting non-fluent variant into three subtypes, while logopenic PPA was split into two subtypes. Voxel-brain mapping analysis displayed different patterns of hypometabolism for each PPA group. New subtypes also showed a different clinical course and were predictive of amyloid imaging results.>Conclusion: Our study found that there are more than the three already recognized subtypes of PPA. These new subtypes were more predictive of clinical course and showed different neuroimaging patterns. Our results support the usefulness of FDG-PET in evaluating PPA, and the applicability of computational methods in the analysis of brain metabolism for improving the classification of neurodegenerative disorders.
机译:>背景:原发性进行性失语症(PPA)是一种临床综合征,其特征是语言大脑系统发生神经变性。已经认识到三种主要的临床形式(非流利的,语义的和低俗的PPA),但是分类的适用性和预测潜在病理的能力尚存争议。我们旨在研究一系列连续病例的PPA患者的FDG-PET影像数据,以根据区域脑代谢将其分为不同的亚型。>方法: 122项91项PPA的FDG-PET影像研究包括患者和28名健康对照。我们使用Ward的链接方法(一种无监督的聚类算法)开发了层次化的聚类分析。我们进行了基于体素的脑图分析,以评估每个识别出的簇的低代谢模式。>结果:簇分析确认了三个当前的PPA变体,但根据Davies-Bouldin指数的最佳簇数为PPA的6个亚型。这种分类是由于将非流利的变体分为三个亚型,而低密度PPA被分为了两个亚型。体素-大脑作图分析显示了每个PPA组的低代谢模式不同。新的亚型还显示出不同的临床过程,并且可以预测淀粉样蛋白的成像结果。>结论:我们的研究发现,PPA的亚型不止三种。这些新的亚型对临床过程更具预测性,并表现出不同的神经影像学模式。我们的结果支持FDG-PET在评估PPA中的有用性,以及计算方法在分析脑代谢以改善神经退行性疾病分类中的适用性。

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