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Infraslow State Fluctuations Govern Spontaneous fMRI Network Dynamics

Spontaneous brain activity as assessed with resting-state fMRI exhibits rich spatiotemporal structure. However, the principles by which brain-wide patterns of spontaneous fMRI activity reconfigure and interact with each other remain unclear. We used a framewise clustering approach to map spatiotempo...

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Autores principales: Gutierrez-Barragan, Daniel, Basson, M. Albert, Panzeri, Stefano, Gozzi, Alessandro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cell Press 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6657681/
https://www.ncbi.nlm.nih.gov/pubmed/31303490
http://dx.doi.org/10.1016/j.cub.2019.06.017
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author Gutierrez-Barragan, Daniel
Basson, M. Albert
Panzeri, Stefano
Gozzi, Alessandro
author_facet Gutierrez-Barragan, Daniel
Basson, M. Albert
Panzeri, Stefano
Gozzi, Alessandro
author_sort Gutierrez-Barragan, Daniel
collection PubMed
description Spontaneous brain activity as assessed with resting-state fMRI exhibits rich spatiotemporal structure. However, the principles by which brain-wide patterns of spontaneous fMRI activity reconfigure and interact with each other remain unclear. We used a framewise clustering approach to map spatiotemporal dynamics of spontaneous fMRI activity with voxel resolution in the resting mouse brain. We show that brain-wide patterns of fMRI co-activation can be reliably mapped at the group and subject level, defining a restricted set of recurring brain states characterized by rich network structure. Importantly, we document that the identified fMRI states exhibit contrasting patterns of functional activity and coupled infraslow network dynamics, with each network state occurring at specific phases of global fMRI signal fluctuations. Finally, we show that autism-associated genetic alterations entail the engagement of atypical functional states and altered infraslow network dynamics. Our results reveal a novel set of fundamental principles guiding the spatiotemporal organization of resting-state fMRI activity and its disruption in brain disorders.
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spelling pubmed-66576812019-08-06 Infraslow State Fluctuations Govern Spontaneous fMRI Network Dynamics Gutierrez-Barragan, Daniel Basson, M. Albert Panzeri, Stefano Gozzi, Alessandro Curr Biol Article Spontaneous brain activity as assessed with resting-state fMRI exhibits rich spatiotemporal structure. However, the principles by which brain-wide patterns of spontaneous fMRI activity reconfigure and interact with each other remain unclear. We used a framewise clustering approach to map spatiotemporal dynamics of spontaneous fMRI activity with voxel resolution in the resting mouse brain. We show that brain-wide patterns of fMRI co-activation can be reliably mapped at the group and subject level, defining a restricted set of recurring brain states characterized by rich network structure. Importantly, we document that the identified fMRI states exhibit contrasting patterns of functional activity and coupled infraslow network dynamics, with each network state occurring at specific phases of global fMRI signal fluctuations. Finally, we show that autism-associated genetic alterations entail the engagement of atypical functional states and altered infraslow network dynamics. Our results reveal a novel set of fundamental principles guiding the spatiotemporal organization of resting-state fMRI activity and its disruption in brain disorders. Cell Press 2019-07-22 /pmc/articles/PMC6657681/ /pubmed/31303490 http://dx.doi.org/10.1016/j.cub.2019.06.017 Text en © 2019 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Article
Gutierrez-Barragan, Daniel
Basson, M. Albert
Panzeri, Stefano
Gozzi, Alessandro
Infraslow State Fluctuations Govern Spontaneous fMRI Network Dynamics
title Infraslow State Fluctuations Govern Spontaneous fMRI Network Dynamics
title_full Infraslow State Fluctuations Govern Spontaneous fMRI Network Dynamics
title_fullStr Infraslow State Fluctuations Govern Spontaneous fMRI Network Dynamics
title_full_unstemmed Infraslow State Fluctuations Govern Spontaneous fMRI Network Dynamics
title_short Infraslow State Fluctuations Govern Spontaneous fMRI Network Dynamics
title_sort infraslow state fluctuations govern spontaneous fmri network dynamics
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6657681/
https://www.ncbi.nlm.nih.gov/pubmed/31303490
http://dx.doi.org/10.1016/j.cub.2019.06.017
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