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个体人类传播性内在脑活动的组织。

Organization of Propagated Intrinsic Brain Activity in Individual Humans.

机构信息

Department of Radiology, Washington University, St. Louis, MO 63110, USA.

Department of Psychiatry, Washington University, St. Louis, MO 63110, USA.

出版信息

Cereb Cortex. 2020 Mar 14;30(3):1716-1734. doi: 10.1093/cercor/bhz198.

Abstract

Spontaneous infra-slow (<0.1 Hz) fluctuations in functional magnetic resonance imaging (fMRI) signals are temporally correlated within large-scale functional brain networks, motivating their use for mapping systems-level brain organization. However, recent electrophysiological and hemodynamic evidence suggest state-dependent propagation of infra-slow fluctuations, implying a functional role for ongoing infra-slow activity. Crucially, the study of infra-slow temporal lag structure has thus far been limited to large groups, as analyzing propagation delays requires extensive data averaging to overcome sampling variability. Here, we use resting-state fMRI data from 11 extensively-sampled individuals to characterize lag structure at the individual level. In addition to stable individual-specific features, we find spatiotemporal topographies in each subject similar to the group average. Notably, we find a set of early regions that are common to all individuals, are preferentially positioned proximal to multiple functional networks, and overlap with brain regions known to respond to diverse behavioral tasks-altogether consistent with a hypothesized ability to broadly influence cortical excitability. Our findings suggest that, like correlation structure, temporal lag structure is a fundamental organizational property of resting-state infra-slow activity.

摘要

功能磁共振成像(fMRI)信号中的自发超慢(<0.1 Hz)波动在大尺度功能脑网络内具有时间相关性,这促使人们将其用于绘制系统水平的大脑组织图。然而,最近的电生理和血液动力学证据表明超慢波动的状态依赖性传播,这意味着持续的超慢活动具有功能作用。至关重要的是,到目前为止,超慢时间滞后结构的研究仅限于大型群体,因为分析传播延迟需要广泛的数据平均化来克服采样变异性。在这里,我们使用 11 名个体进行了广泛采样的静息态 fMRI 数据来描述个体水平的滞后结构。除了稳定的个体特定特征外,我们还发现每个主体的时空拓扑结构与组平均值相似。值得注意的是,我们发现了一组早期区域,这些区域存在于所有个体中,优先位于多个功能网络附近,并与已知对各种行为任务有反应的大脑区域重叠——这与假设的广泛影响皮质兴奋性的能力是一致的。我们的发现表明,与相关结构一样,时间滞后结构是静息状态超慢活动的基本组织特性。

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