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额颞叶痴呆额叶变异型中代谢性脑簇的分解

Decomposition of metabolic brain clusters in the frontal variant of frontotemporal dementia.

作者信息

Salmon Eric, Kerrouche Nacer, Herholz Karl, Perani Daniela, Holthoff Vjera, Beuthien-Baumann Bettina, Degueldre Christian, Lemaire Christian, Luxen André, Baron Jean-Claude, Collette Fabienne, Garraux Gaëtan

机构信息

Cyclotron Research Centre, University of Liege, B30 Sart Tilman, 4000 Liège, Belgium.

出版信息

Neuroimage. 2006 Apr 15;30(3):871-8. doi: 10.1016/j.neuroimage.2005.10.016. Epub 2005 Dec 15.

Abstract

Previous studies that measured brain activity in frontotemporal dementia (FTD) used univariate analyses, examining each region of interest separately. We explored in a multicenter European research program the principal brain clusters characterized by a common variability in cerebral metabolism in FTD. Seventy patients with frontal variant (fv) FTD were selected according to international clinical recommendations; principal component analysis (PCA) was performed on FDG-PET metabolic images, looking for covariance clusters in this large population. A first metabolic cluster included most of the lateral and medial prefrontal cortex, bilaterally; PC1 scores correlated with performances on memory and executive neuropsychological tasks. Moreover, FDG-PET images in fv-FTD were further characterized by a metabolic covariance in two clusters comprising the subcallosal medial frontal region, the temporal pole, medial temporal structures and the striatum, separately in the left and in the right hemisphere. The study provides original data-driven arguments for metabolic involvement of separate brain clusters in the rostral limbic system, corresponding to pathological poles differentially affected in each FTD patient.

摘要

以往测量额颞叶痴呆(FTD)脑活动的研究采用单变量分析,分别检查每个感兴趣区域。我们在一个欧洲多中心研究项目中探索了FTD中以大脑代谢共同变异性为特征的主要脑簇。根据国际临床建议,选择了70例额叶变异型(fv)FTD患者;对FDG-PET代谢图像进行主成分分析(PCA),在这一庞大群体中寻找协方差簇。第一个代谢簇包括双侧大部分外侧和内侧前额叶皮质;PC1评分与记忆和执行神经心理学任务的表现相关。此外,fv-FTD的FDG-PET图像的进一步特征是在两个簇中存在代谢协方差,这两个簇分别包括胼胝体下内侧额叶区域、颞极、内侧颞叶结构和纹状体,分别位于左半球和右半球。该研究为 Rostral 边缘系统中不同脑簇的代谢参与提供了原始的数据驱动论据,这与每个FTD患者中受不同影响的病理极点相对应。

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