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Cortical electrophysiological evidence for individual‐specific temporal organization of brain functional networks

The human brain has been demonstrated to rapidly and continuously form and dissolve networks on a subsecond timescale, offering effective and essential substrates for cognitive processes. Understanding how the dynamic organization of brain functional networks on a subsecond level varies across indiv...

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Autores principales: Shu, Su, Qin, Lang, Yin, Yayan, Han, Meizhen, Cui, Wei, Gao, Jia‐Hong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons, Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7267903/
https://www.ncbi.nlm.nih.gov/pubmed/31961469
http://dx.doi.org/10.1002/hbm.24937
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author Shu, Su
Qin, Lang
Yin, Yayan
Han, Meizhen
Cui, Wei
Gao, Jia‐Hong
author_facet Shu, Su
Qin, Lang
Yin, Yayan
Han, Meizhen
Cui, Wei
Gao, Jia‐Hong
author_sort Shu, Su
collection PubMed
description The human brain has been demonstrated to rapidly and continuously form and dissolve networks on a subsecond timescale, offering effective and essential substrates for cognitive processes. Understanding how the dynamic organization of brain functional networks on a subsecond level varies across individuals is, therefore, of great interest for personalized neuroscience. However, it remains unclear whether features of such rapid network organization are reliably unique and stable in single subjects and, therefore, can be used in characterizing individual networks. Here, we used two sets of 5‐min magnetoencephalography (MEG) resting data from 39 healthy subjects over two consecutive days and modeled the spontaneous brain activity as recurring networks fast shifting between each other in a coordinated manner. MEG cortical maps were obtained through source reconstruction using the beamformer method and subjects' temporal structure of recurring networks was obtained via the Hidden Markov Model. Individual organization of dynamic brain activity was quantified with the features of the network‐switching pattern (i.e., transition probability and mean interval time) and the time‐allocation mode (i.e., fractional occupancy and mean lifetime). Using these features, we were able to identify subjects from the group with significant accuracies (~40% on average in 0.5–48 Hz). Notably, the default mode network displayed a distinguishable pattern, being the least frequently visited network with the longest duration for each visit. Together, we provide initial evidence suggesting that the rapid dynamic temporal organization of brain networks achieved in electrophysiology is intrinsic and subject specific.
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spelling pubmed-72679032020-06-12 Cortical electrophysiological evidence for individual‐specific temporal organization of brain functional networks Shu, Su Qin, Lang Yin, Yayan Han, Meizhen Cui, Wei Gao, Jia‐Hong Hum Brain Mapp Research Articles The human brain has been demonstrated to rapidly and continuously form and dissolve networks on a subsecond timescale, offering effective and essential substrates for cognitive processes. Understanding how the dynamic organization of brain functional networks on a subsecond level varies across individuals is, therefore, of great interest for personalized neuroscience. However, it remains unclear whether features of such rapid network organization are reliably unique and stable in single subjects and, therefore, can be used in characterizing individual networks. Here, we used two sets of 5‐min magnetoencephalography (MEG) resting data from 39 healthy subjects over two consecutive days and modeled the spontaneous brain activity as recurring networks fast shifting between each other in a coordinated manner. MEG cortical maps were obtained through source reconstruction using the beamformer method and subjects' temporal structure of recurring networks was obtained via the Hidden Markov Model. Individual organization of dynamic brain activity was quantified with the features of the network‐switching pattern (i.e., transition probability and mean interval time) and the time‐allocation mode (i.e., fractional occupancy and mean lifetime). Using these features, we were able to identify subjects from the group with significant accuracies (~40% on average in 0.5–48 Hz). Notably, the default mode network displayed a distinguishable pattern, being the least frequently visited network with the longest duration for each visit. Together, we provide initial evidence suggesting that the rapid dynamic temporal organization of brain networks achieved in electrophysiology is intrinsic and subject specific. John Wiley & Sons, Inc. 2020-01-21 /pmc/articles/PMC7267903/ /pubmed/31961469 http://dx.doi.org/10.1002/hbm.24937 Text en © 2020 The Authors. Human Brain Mapping published by Wiley Periodicals, Inc. This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.
spellingShingle Research Articles
Shu, Su
Qin, Lang
Yin, Yayan
Han, Meizhen
Cui, Wei
Gao, Jia‐Hong
Cortical electrophysiological evidence for individual‐specific temporal organization of brain functional networks
title Cortical electrophysiological evidence for individual‐specific temporal organization of brain functional networks
title_full Cortical electrophysiological evidence for individual‐specific temporal organization of brain functional networks
title_fullStr Cortical electrophysiological evidence for individual‐specific temporal organization of brain functional networks
title_full_unstemmed Cortical electrophysiological evidence for individual‐specific temporal organization of brain functional networks
title_short Cortical electrophysiological evidence for individual‐specific temporal organization of brain functional networks
title_sort cortical electrophysiological evidence for individual‐specific temporal organization of brain functional networks
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7267903/
https://www.ncbi.nlm.nih.gov/pubmed/31961469
http://dx.doi.org/10.1002/hbm.24937
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