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A spatiotemporal complexity architecture of human brain activity

The human brain operates in large-scale functional networks. These networks are an expression of temporally correlated activity across brain regions, but how global network properties relate to the neural dynamics of individual regions remains incompletely understood. Here, we show that the brain’s...

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Autores principales: Krohn, Stephan, von Schwanenflug, Nina, Waschke, Leonhard, Romanello, Amy, Gell, Martin, Garrett, Douglas D., Finke, Carsten
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Association for the Advancement of Science 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9891702/
https://www.ncbi.nlm.nih.gov/pubmed/36724223
http://dx.doi.org/10.1126/sciadv.abq3851
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author Krohn, Stephan
von Schwanenflug, Nina
Waschke, Leonhard
Romanello, Amy
Gell, Martin
Garrett, Douglas D.
Finke, Carsten
author_facet Krohn, Stephan
von Schwanenflug, Nina
Waschke, Leonhard
Romanello, Amy
Gell, Martin
Garrett, Douglas D.
Finke, Carsten
author_sort Krohn, Stephan
collection PubMed
description The human brain operates in large-scale functional networks. These networks are an expression of temporally correlated activity across brain regions, but how global network properties relate to the neural dynamics of individual regions remains incompletely understood. Here, we show that the brain’s network architecture is tightly linked to critical episodes of neural regularity, visible as spontaneous “complexity drops” in functional magnetic resonance imaging signals. These episodes closely explain functional connectivity strength between regions, subserve the propagation of neural activity patterns, and reflect interindividual differences in age and behavior. Furthermore, complexity drops define neural activity states that dynamically shape the connectivity strength, topological configuration, and hierarchy of brain networks and comprehensively explain known structure-function relationships within the brain. These findings delineate a principled complexity architecture of neural activity—a human “complexome” that underpins the brain’s functional network organization.
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spelling pubmed-98917022023-02-08 A spatiotemporal complexity architecture of human brain activity Krohn, Stephan von Schwanenflug, Nina Waschke, Leonhard Romanello, Amy Gell, Martin Garrett, Douglas D. Finke, Carsten Sci Adv Neuroscience The human brain operates in large-scale functional networks. These networks are an expression of temporally correlated activity across brain regions, but how global network properties relate to the neural dynamics of individual regions remains incompletely understood. Here, we show that the brain’s network architecture is tightly linked to critical episodes of neural regularity, visible as spontaneous “complexity drops” in functional magnetic resonance imaging signals. These episodes closely explain functional connectivity strength between regions, subserve the propagation of neural activity patterns, and reflect interindividual differences in age and behavior. Furthermore, complexity drops define neural activity states that dynamically shape the connectivity strength, topological configuration, and hierarchy of brain networks and comprehensively explain known structure-function relationships within the brain. These findings delineate a principled complexity architecture of neural activity—a human “complexome” that underpins the brain’s functional network organization. American Association for the Advancement of Science 2023-02-01 /pmc/articles/PMC9891702/ /pubmed/36724223 http://dx.doi.org/10.1126/sciadv.abq3851 Text en Copyright © 2023 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works. Distributed under a Creative Commons Attribution NonCommercial License 4.0 (CC BY-NC). https://creativecommons.org/licenses/by-nc/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial license (https://creativecommons.org/licenses/by-nc/4.0/) , which permits use, distribution, and reproduction in any medium, so long as the resultant use is not for commercial advantage and provided the original work is properly cited.
spellingShingle Neuroscience
Krohn, Stephan
von Schwanenflug, Nina
Waschke, Leonhard
Romanello, Amy
Gell, Martin
Garrett, Douglas D.
Finke, Carsten
A spatiotemporal complexity architecture of human brain activity
title A spatiotemporal complexity architecture of human brain activity
title_full A spatiotemporal complexity architecture of human brain activity
title_fullStr A spatiotemporal complexity architecture of human brain activity
title_full_unstemmed A spatiotemporal complexity architecture of human brain activity
title_short A spatiotemporal complexity architecture of human brain activity
title_sort spatiotemporal complexity architecture of human brain activity
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9891702/
https://www.ncbi.nlm.nih.gov/pubmed/36724223
http://dx.doi.org/10.1126/sciadv.abq3851
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