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Resting-State Temporal Synchronization Networks Emerge from Connectivity Topology and Heterogeneity

Spatial patterns of coherent activity across different brain areas have been identified during the resting-state fluctuations of the brain. However, recent studies indicate that resting-state activity is not stationary, but shows complex temporal dynamics. We were interested in the spatiotemporal dy...

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Autores principales: Ponce-Alvarez, Adrián, Deco, Gustavo, Hagmann, Patric, Romani, Gian Luca, Mantini, Dante, Corbetta, Maurizio
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4333573/
https://www.ncbi.nlm.nih.gov/pubmed/25692996
http://dx.doi.org/10.1371/journal.pcbi.1004100
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author Ponce-Alvarez, Adrián
Deco, Gustavo
Hagmann, Patric
Romani, Gian Luca
Mantini, Dante
Corbetta, Maurizio
author_facet Ponce-Alvarez, Adrián
Deco, Gustavo
Hagmann, Patric
Romani, Gian Luca
Mantini, Dante
Corbetta, Maurizio
author_sort Ponce-Alvarez, Adrián
collection PubMed
description Spatial patterns of coherent activity across different brain areas have been identified during the resting-state fluctuations of the brain. However, recent studies indicate that resting-state activity is not stationary, but shows complex temporal dynamics. We were interested in the spatiotemporal dynamics of the phase interactions among resting-state fMRI BOLD signals from human subjects. We found that the global phase synchrony of the BOLD signals evolves on a characteristic ultra-slow (<0.01Hz) time scale, and that its temporal variations reflect the transient formation and dissolution of multiple communities of synchronized brain regions. Synchronized communities reoccurred intermittently in time and across scanning sessions. We found that the synchronization communities relate to previously defined functional networks known to be engaged in sensory-motor or cognitive function, called resting-state networks (RSNs), including the default mode network, the somato-motor network, the visual network, the auditory network, the cognitive control networks, the self-referential network, and combinations of these and other RSNs. We studied the mechanism originating the observed spatiotemporal synchronization dynamics by using a network model of phase oscillators connected through the brain’s anatomical connectivity estimated using diffusion imaging human data. The model consistently approximates the temporal and spatial synchronization patterns of the empirical data, and reveals that multiple clusters that transiently synchronize and desynchronize emerge from the complex topology of anatomical connections, provided that oscillators are heterogeneous.
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spelling pubmed-43335732015-02-24 Resting-State Temporal Synchronization Networks Emerge from Connectivity Topology and Heterogeneity Ponce-Alvarez, Adrián Deco, Gustavo Hagmann, Patric Romani, Gian Luca Mantini, Dante Corbetta, Maurizio PLoS Comput Biol Research Article Spatial patterns of coherent activity across different brain areas have been identified during the resting-state fluctuations of the brain. However, recent studies indicate that resting-state activity is not stationary, but shows complex temporal dynamics. We were interested in the spatiotemporal dynamics of the phase interactions among resting-state fMRI BOLD signals from human subjects. We found that the global phase synchrony of the BOLD signals evolves on a characteristic ultra-slow (<0.01Hz) time scale, and that its temporal variations reflect the transient formation and dissolution of multiple communities of synchronized brain regions. Synchronized communities reoccurred intermittently in time and across scanning sessions. We found that the synchronization communities relate to previously defined functional networks known to be engaged in sensory-motor or cognitive function, called resting-state networks (RSNs), including the default mode network, the somato-motor network, the visual network, the auditory network, the cognitive control networks, the self-referential network, and combinations of these and other RSNs. We studied the mechanism originating the observed spatiotemporal synchronization dynamics by using a network model of phase oscillators connected through the brain’s anatomical connectivity estimated using diffusion imaging human data. The model consistently approximates the temporal and spatial synchronization patterns of the empirical data, and reveals that multiple clusters that transiently synchronize and desynchronize emerge from the complex topology of anatomical connections, provided that oscillators are heterogeneous. Public Library of Science 2015-02-18 /pmc/articles/PMC4333573/ /pubmed/25692996 http://dx.doi.org/10.1371/journal.pcbi.1004100 Text en https://creativecommons.org/publicdomain/zero/1.0/ This is an open-access article distributed under the terms of the Creative Commons Public Domain declaration, which stipulates that, once placed in the public domain, this work may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose.
spellingShingle Research Article
Ponce-Alvarez, Adrián
Deco, Gustavo
Hagmann, Patric
Romani, Gian Luca
Mantini, Dante
Corbetta, Maurizio
Resting-State Temporal Synchronization Networks Emerge from Connectivity Topology and Heterogeneity
title Resting-State Temporal Synchronization Networks Emerge from Connectivity Topology and Heterogeneity
title_full Resting-State Temporal Synchronization Networks Emerge from Connectivity Topology and Heterogeneity
title_fullStr Resting-State Temporal Synchronization Networks Emerge from Connectivity Topology and Heterogeneity
title_full_unstemmed Resting-State Temporal Synchronization Networks Emerge from Connectivity Topology and Heterogeneity
title_short Resting-State Temporal Synchronization Networks Emerge from Connectivity Topology and Heterogeneity
title_sort resting-state temporal synchronization networks emerge from connectivity topology and heterogeneity
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4333573/
https://www.ncbi.nlm.nih.gov/pubmed/25692996
http://dx.doi.org/10.1371/journal.pcbi.1004100
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