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The Transitions Between Dynamic Micro-States Reveal Age-Related Functional Network Reorganization

Normal dynamic change in human brain occurs with age increasing, yet much remains unknown regarding how brain develops, matures, and ages. Functional connectivity analysis of the resting-state brain is a powerful method for revealing the intrinsic features of functional networks, and micro-states, w...

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Autores principales: Chen, Yuanyuan, Liu, Ya-nan, Zhou, Peng, Zhang, Xiong, Wu, Qiong, Zhao, Xin, Ming, Dong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6328489/
https://www.ncbi.nlm.nih.gov/pubmed/30662409
http://dx.doi.org/10.3389/fphys.2018.01852
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author Chen, Yuanyuan
Liu, Ya-nan
Zhou, Peng
Zhang, Xiong
Wu, Qiong
Zhao, Xin
Ming, Dong
author_facet Chen, Yuanyuan
Liu, Ya-nan
Zhou, Peng
Zhang, Xiong
Wu, Qiong
Zhao, Xin
Ming, Dong
author_sort Chen, Yuanyuan
collection PubMed
description Normal dynamic change in human brain occurs with age increasing, yet much remains unknown regarding how brain develops, matures, and ages. Functional connectivity analysis of the resting-state brain is a powerful method for revealing the intrinsic features of functional networks, and micro-states, which are the intrinsic patterns of functional connectivity in dynamic network courses, and are suggested to be more informative of brain functional changes. The aim of this study is to explore the age-related changes in these micro-states of dynamic functional network. Three healthy groups were included: the young (ages 21–32 years), the adult (age 41–54 years), and the old (age 60–86 years). Sliding window correlation method was used to construct the dynamic connectivity networks, and then the micro-states were individually identified with clustering analysis. The distribution of age-related connectivity variations in several intrinsic networks for each micro-state was analyzed then. The micro-states showed substantial age-related changes in the transitions between states but not in the dwelling time. Also there was no age-related reorganization observed within any micro-state. But there were reorganizations observed in the transition between them. These results suggested that the identified micro-states represented certain underlying connectivity patterns in functional brain system, which are similar to the intrinsic cognitive networks or resources. In addition, the dynamic transitions between these states were probable mechanisms of reorganization or compensation in functional brain networks with age increasing.
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spelling pubmed-63284892019-01-18 The Transitions Between Dynamic Micro-States Reveal Age-Related Functional Network Reorganization Chen, Yuanyuan Liu, Ya-nan Zhou, Peng Zhang, Xiong Wu, Qiong Zhao, Xin Ming, Dong Front Physiol Physiology Normal dynamic change in human brain occurs with age increasing, yet much remains unknown regarding how brain develops, matures, and ages. Functional connectivity analysis of the resting-state brain is a powerful method for revealing the intrinsic features of functional networks, and micro-states, which are the intrinsic patterns of functional connectivity in dynamic network courses, and are suggested to be more informative of brain functional changes. The aim of this study is to explore the age-related changes in these micro-states of dynamic functional network. Three healthy groups were included: the young (ages 21–32 years), the adult (age 41–54 years), and the old (age 60–86 years). Sliding window correlation method was used to construct the dynamic connectivity networks, and then the micro-states were individually identified with clustering analysis. The distribution of age-related connectivity variations in several intrinsic networks for each micro-state was analyzed then. The micro-states showed substantial age-related changes in the transitions between states but not in the dwelling time. Also there was no age-related reorganization observed within any micro-state. But there were reorganizations observed in the transition between them. These results suggested that the identified micro-states represented certain underlying connectivity patterns in functional brain system, which are similar to the intrinsic cognitive networks or resources. In addition, the dynamic transitions between these states were probable mechanisms of reorganization or compensation in functional brain networks with age increasing. Frontiers Media S.A. 2019-01-04 /pmc/articles/PMC6328489/ /pubmed/30662409 http://dx.doi.org/10.3389/fphys.2018.01852 Text en Copyright © 2019 Chen, Liu, Zhou, Zhang, Wu, Zhao and Ming. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Physiology
Chen, Yuanyuan
Liu, Ya-nan
Zhou, Peng
Zhang, Xiong
Wu, Qiong
Zhao, Xin
Ming, Dong
The Transitions Between Dynamic Micro-States Reveal Age-Related Functional Network Reorganization
title The Transitions Between Dynamic Micro-States Reveal Age-Related Functional Network Reorganization
title_full The Transitions Between Dynamic Micro-States Reveal Age-Related Functional Network Reorganization
title_fullStr The Transitions Between Dynamic Micro-States Reveal Age-Related Functional Network Reorganization
title_full_unstemmed The Transitions Between Dynamic Micro-States Reveal Age-Related Functional Network Reorganization
title_short The Transitions Between Dynamic Micro-States Reveal Age-Related Functional Network Reorganization
title_sort transitions between dynamic micro-states reveal age-related functional network reorganization
topic Physiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6328489/
https://www.ncbi.nlm.nih.gov/pubmed/30662409
http://dx.doi.org/10.3389/fphys.2018.01852
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