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Age-related changes of whole-brain dynamics in spontaneous neuronal coactivations

Human brains experience whole-brain anatomic and functional changes throughout the lifespan. Age-related whole-brain network changes have been studied with functional magnetic resonance imaging (fMRI) to determine their low-frequency spatial and temporal characteristics. However, little is known abo...

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Autores principales: Shou, Guofa, Yuan, Han, Cha, Yoon-Hee, Sweeney, John A., Ding, Lei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9287374/
https://www.ncbi.nlm.nih.gov/pubmed/35840643
http://dx.doi.org/10.1038/s41598-022-16125-2
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author Shou, Guofa
Yuan, Han
Cha, Yoon-Hee
Sweeney, John A.
Ding, Lei
author_facet Shou, Guofa
Yuan, Han
Cha, Yoon-Hee
Sweeney, John A.
Ding, Lei
author_sort Shou, Guofa
collection PubMed
description Human brains experience whole-brain anatomic and functional changes throughout the lifespan. Age-related whole-brain network changes have been studied with functional magnetic resonance imaging (fMRI) to determine their low-frequency spatial and temporal characteristics. However, little is known about age-related changes in whole-brain fast dynamics at the scale of neuronal events. The present study investigated age-related whole-brain dynamics in resting-state electroencephalography (EEG) signals from 73 healthy participants from 6 to 65 years old via characterizing transient neuronal coactivations at a resolution of tens of milliseconds. These uncovered transient patterns suggest fluctuating brain states at different energy levels of global activations. Our results indicate that with increasing age, shorter lifetimes and more occurrences were observed in the brain states that show the global high activations and more consecutive visits to the global highest-activation brain state. There were also reduced transitional steps during consecutive visits to the global lowest-activation brain state. These age-related effects suggest reduced stability and increased fluctuations when visiting high-energy brain states and with a bias toward staying low-energy brain states. These age-related whole-brain dynamics changes are further supported by changes observed in classic alpha and beta power, suggesting its promising applications in examining the effect of normal healthy brain aging, brain development, and brain disease.
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spelling pubmed-92873742022-07-17 Age-related changes of whole-brain dynamics in spontaneous neuronal coactivations Shou, Guofa Yuan, Han Cha, Yoon-Hee Sweeney, John A. Ding, Lei Sci Rep Article Human brains experience whole-brain anatomic and functional changes throughout the lifespan. Age-related whole-brain network changes have been studied with functional magnetic resonance imaging (fMRI) to determine their low-frequency spatial and temporal characteristics. However, little is known about age-related changes in whole-brain fast dynamics at the scale of neuronal events. The present study investigated age-related whole-brain dynamics in resting-state electroencephalography (EEG) signals from 73 healthy participants from 6 to 65 years old via characterizing transient neuronal coactivations at a resolution of tens of milliseconds. These uncovered transient patterns suggest fluctuating brain states at different energy levels of global activations. Our results indicate that with increasing age, shorter lifetimes and more occurrences were observed in the brain states that show the global high activations and more consecutive visits to the global highest-activation brain state. There were also reduced transitional steps during consecutive visits to the global lowest-activation brain state. These age-related effects suggest reduced stability and increased fluctuations when visiting high-energy brain states and with a bias toward staying low-energy brain states. These age-related whole-brain dynamics changes are further supported by changes observed in classic alpha and beta power, suggesting its promising applications in examining the effect of normal healthy brain aging, brain development, and brain disease. Nature Publishing Group UK 2022-07-15 /pmc/articles/PMC9287374/ /pubmed/35840643 http://dx.doi.org/10.1038/s41598-022-16125-2 Text en © The Author(s) 2022 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Shou, Guofa
Yuan, Han
Cha, Yoon-Hee
Sweeney, John A.
Ding, Lei
Age-related changes of whole-brain dynamics in spontaneous neuronal coactivations
title Age-related changes of whole-brain dynamics in spontaneous neuronal coactivations
title_full Age-related changes of whole-brain dynamics in spontaneous neuronal coactivations
title_fullStr Age-related changes of whole-brain dynamics in spontaneous neuronal coactivations
title_full_unstemmed Age-related changes of whole-brain dynamics in spontaneous neuronal coactivations
title_short Age-related changes of whole-brain dynamics in spontaneous neuronal coactivations
title_sort age-related changes of whole-brain dynamics in spontaneous neuronal coactivations
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9287374/
https://www.ncbi.nlm.nih.gov/pubmed/35840643
http://dx.doi.org/10.1038/s41598-022-16125-2
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