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Critical scaling of whole-brain resting-state dynamics
Scale invariance is a characteristic of neural activity. How this property emerges from neural interactions remains a fundamental question. Here, we studied the relation between scale-invariant brain dynamics and structural connectivity by analyzing human resting-state (rs-) fMRI signals, together w...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10257708/ https://www.ncbi.nlm.nih.gov/pubmed/37301936 http://dx.doi.org/10.1038/s42003-023-05001-y |
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author | Ponce-Alvarez, Adrián Kringelbach, Morten L. Deco, Gustavo |
author_facet | Ponce-Alvarez, Adrián Kringelbach, Morten L. Deco, Gustavo |
author_sort | Ponce-Alvarez, Adrián |
collection | PubMed |
description | Scale invariance is a characteristic of neural activity. How this property emerges from neural interactions remains a fundamental question. Here, we studied the relation between scale-invariant brain dynamics and structural connectivity by analyzing human resting-state (rs-) fMRI signals, together with diffusion MRI (dMRI) connectivity and its approximation as an exponentially decaying function of the distance between brain regions. We analyzed the rs-fMRI dynamics using functional connectivity and a recently proposed phenomenological renormalization group (PRG) method that tracks the change of collective activity after successive coarse-graining at different scales. We found that brain dynamics display power-law correlations and power-law scaling as a function of PRG coarse-graining based on functional or structural connectivity. Moreover, we modeled the brain activity using a network of spins interacting through large-scale connectivity and presenting a phase transition between ordered and disordered phases. Within this simple model, we found that the observed scaling features were likely to emerge from critical dynamics and connections exponentially decaying with distance. In conclusion, our study tests the PRG method using large-scale brain activity and theoretical models and suggests that scaling of rs-fMRI activity relates to criticality. |
format | Online Article Text |
id | pubmed-10257708 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-102577082023-06-12 Critical scaling of whole-brain resting-state dynamics Ponce-Alvarez, Adrián Kringelbach, Morten L. Deco, Gustavo Commun Biol Article Scale invariance is a characteristic of neural activity. How this property emerges from neural interactions remains a fundamental question. Here, we studied the relation between scale-invariant brain dynamics and structural connectivity by analyzing human resting-state (rs-) fMRI signals, together with diffusion MRI (dMRI) connectivity and its approximation as an exponentially decaying function of the distance between brain regions. We analyzed the rs-fMRI dynamics using functional connectivity and a recently proposed phenomenological renormalization group (PRG) method that tracks the change of collective activity after successive coarse-graining at different scales. We found that brain dynamics display power-law correlations and power-law scaling as a function of PRG coarse-graining based on functional or structural connectivity. Moreover, we modeled the brain activity using a network of spins interacting through large-scale connectivity and presenting a phase transition between ordered and disordered phases. Within this simple model, we found that the observed scaling features were likely to emerge from critical dynamics and connections exponentially decaying with distance. In conclusion, our study tests the PRG method using large-scale brain activity and theoretical models and suggests that scaling of rs-fMRI activity relates to criticality. Nature Publishing Group UK 2023-06-10 /pmc/articles/PMC10257708/ /pubmed/37301936 http://dx.doi.org/10.1038/s42003-023-05001-y Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Ponce-Alvarez, Adrián Kringelbach, Morten L. Deco, Gustavo Critical scaling of whole-brain resting-state dynamics |
title | Critical scaling of whole-brain resting-state dynamics |
title_full | Critical scaling of whole-brain resting-state dynamics |
title_fullStr | Critical scaling of whole-brain resting-state dynamics |
title_full_unstemmed | Critical scaling of whole-brain resting-state dynamics |
title_short | Critical scaling of whole-brain resting-state dynamics |
title_sort | critical scaling of whole-brain resting-state dynamics |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10257708/ https://www.ncbi.nlm.nih.gov/pubmed/37301936 http://dx.doi.org/10.1038/s42003-023-05001-y |
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