全球 fMRI 信号拓扑中的系统性横截面年龄关联

Jason S. Nomi, Danilo Bzdok, Jingwei Li, Taylor Bolt, Catie Chang, S. Kornfeld, Z. Goodman, B.T. Thomas Yeo, R. N. Spreng, L. Uddin
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摘要

摘要 静止态功能磁共振成像(fMRI)中的全局信号(GS)已知包含伪影和非神经元生理信号,但也包含与个体状态和特征相关的重要神经信息。在这里,我们在一个横断面样本中(6-85 岁)显示了 GS 拓扑图与年龄之间明显的线性和曲线关系,这些样本代表了人一生中的重要部分。丘脑和普鲁士门等皮层下脑区在不同年龄段显示出与 GS 的线性关系。与年轻人相比,丘脑对老年人GS的贡献更大,而与老年人相比,丘脑对年轻人GS的贡献更大。皮层下的梅内特基底核(nucleus basalis of Meynert)显示出与外侧额顶叶网络和背侧注意网络内的皮层区域类似的 U 形模式,即 GS 的贡献在早期和老年期较强,而在中年期较弱。大脑皮层下和大脑皮层的活动在不同年龄段的这种分化支持 GS 构成的双层模型,即 GS 的皮层下部分与 GS 的皮层部分有所区别。我们发现,在人类的整个发展过程中,皮层下和皮层对 GS 的贡献与年龄密切相关。我们的研究结果表明,在不同的发育过程中,GS 内的神经生物学信息是如何不同的,并强调在研究与年龄相关的大脑功能差异时,需要仔细考虑是否要去除这一信号。
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Systematic cross-sectional age-associations in global fMRI signal topography
Abstract The global signal (GS) in resting-state functional MRI (fMRI), known to contain artifacts and non-neuronal physiological signals, also contains important neural information related to individual state and trait characteristics. Here, we show distinct linear and curvilinear relationships between GS topography and age in a cross-sectional sample of individuals (6-85 years old) representing a significant portion of the lifespan. Subcortical brain regions such as the thalamus and putamen show linear associations with the GS across age. The thalamus has stronger contributions to the GS in older-age individuals compared with younger-aged individuals, while the putamen has stronger contributions in younger individuals compared with older individuals. The subcortical nucleus basalis of Meynert shows a u-shaped pattern similar to cortical regions within the lateral frontoparietal network and dorsal attention network, where contributions of the GS are stronger at early and old age, and weaker in middle age. This differentiation between subcortical and cortical brain activity across age supports a dual-layer model of GS composition, where subcortical aspects of the GS are differentiated from cortical aspects of the GS. We find that these subcortical-cortical contributions to the GS depend strongly on age across the lifespan of human development. Our findings demonstrate how neurobiological information within the GS differs across development and highlight the need to carefully consider whether or not to remove this signal when investigating age-related functional differences in the brain.
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