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Modular co-organization of functional connectivity and scale-free dynamics in the human brain

Scale-free neuronal dynamics and interareal correlations are emergent characteristics of spontaneous brain activity. How such dynamics and the anatomical patterns of neuronal connectivity are mutually related in brain networks has, however, remained unclear. We addressed this relationship by quantif...

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Autores principales: Zhigalov, Alexander, Arnulfo, Gabriele, Nobili, Lino, Palva, Satu, Palva, J. Matias
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MIT Press 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5988393/
https://www.ncbi.nlm.nih.gov/pubmed/29911674
http://dx.doi.org/10.1162/NETN_a_00008
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author Zhigalov, Alexander
Arnulfo, Gabriele
Nobili, Lino
Palva, Satu
Palva, J. Matias
author_facet Zhigalov, Alexander
Arnulfo, Gabriele
Nobili, Lino
Palva, Satu
Palva, J. Matias
author_sort Zhigalov, Alexander
collection PubMed
description Scale-free neuronal dynamics and interareal correlations are emergent characteristics of spontaneous brain activity. How such dynamics and the anatomical patterns of neuronal connectivity are mutually related in brain networks has, however, remained unclear. We addressed this relationship by quantifying the network colocalization of scale-free neuronal activity—both neuronal avalanches and long-range temporal correlations (LRTCs)—and functional connectivity (FC) by means of intracranial and noninvasive human resting-state electrophysiological recordings. We found frequency-specific colocalization of scale-free dynamics and FC so that the interareal couplings of LRTCs and the propagation of neuronal avalanches were most pronounced in the predominant pathways of FC. Several control analyses and the frequency specificity of network colocalization showed that the results were not trivial by-products of either brain dynamics or our analysis approach. Crucially, scale-free neuronal dynamics and connectivity also had colocalized modular structures at multiple levels of network organization, suggesting that modules of FC would be endowed with partially independent dynamic states. These findings thus suggest that FC and scale-free dynamics—hence, putatively, neuronal criticality as well—coemerge in a hierarchically modular structure in which the modules are characterized by dense connectivity, avalanche propagation, and shared dynamic states.
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spelling pubmed-59883932018-06-15 Modular co-organization of functional connectivity and scale-free dynamics in the human brain Zhigalov, Alexander Arnulfo, Gabriele Nobili, Lino Palva, Satu Palva, J. Matias Netw Neurosci Research Scale-free neuronal dynamics and interareal correlations are emergent characteristics of spontaneous brain activity. How such dynamics and the anatomical patterns of neuronal connectivity are mutually related in brain networks has, however, remained unclear. We addressed this relationship by quantifying the network colocalization of scale-free neuronal activity—both neuronal avalanches and long-range temporal correlations (LRTCs)—and functional connectivity (FC) by means of intracranial and noninvasive human resting-state electrophysiological recordings. We found frequency-specific colocalization of scale-free dynamics and FC so that the interareal couplings of LRTCs and the propagation of neuronal avalanches were most pronounced in the predominant pathways of FC. Several control analyses and the frequency specificity of network colocalization showed that the results were not trivial by-products of either brain dynamics or our analysis approach. Crucially, scale-free neuronal dynamics and connectivity also had colocalized modular structures at multiple levels of network organization, suggesting that modules of FC would be endowed with partially independent dynamic states. These findings thus suggest that FC and scale-free dynamics—hence, putatively, neuronal criticality as well—coemerge in a hierarchically modular structure in which the modules are characterized by dense connectivity, avalanche propagation, and shared dynamic states. MIT Press 2017-06-01 /pmc/articles/PMC5988393/ /pubmed/29911674 http://dx.doi.org/10.1162/NETN_a_00008 Text en © 2017 Massachusetts Institute of Technology http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Zhigalov, Alexander
Arnulfo, Gabriele
Nobili, Lino
Palva, Satu
Palva, J. Matias
Modular co-organization of functional connectivity and scale-free dynamics in the human brain
title Modular co-organization of functional connectivity and scale-free dynamics in the human brain
title_full Modular co-organization of functional connectivity and scale-free dynamics in the human brain
title_fullStr Modular co-organization of functional connectivity and scale-free dynamics in the human brain
title_full_unstemmed Modular co-organization of functional connectivity and scale-free dynamics in the human brain
title_short Modular co-organization of functional connectivity and scale-free dynamics in the human brain
title_sort modular co-organization of functional connectivity and scale-free dynamics in the human brain
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5988393/
https://www.ncbi.nlm.nih.gov/pubmed/29911674
http://dx.doi.org/10.1162/NETN_a_00008
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