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Spontaneous cortical MEG activity undergoes unique age- and sex-related changes during the transition to adolescence

BACKGROUND: While numerous studies have examined the developmental trajectory of task-based neural oscillations during childhood and adolescence, far less is known about the evolution of spontaneous cortical activity during this time period. Likewise, many studies have shown robust sex differences i...

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Autores principales: Ott, Lauren R., Penhale, Samantha H., Taylor, Brittany K., Lew, Brandon J., Wang, Yu-Ping, Calhoun, Vince D., Stephen, Julia M., Wilson, Tony W.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8685767/
https://www.ncbi.nlm.nih.gov/pubmed/34517128
http://dx.doi.org/10.1016/j.neuroimage.2021.118552
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author Ott, Lauren R.
Penhale, Samantha H.
Taylor, Brittany K.
Lew, Brandon J.
Wang, Yu-Ping
Calhoun, Vince D.
Stephen, Julia M.
Wilson, Tony W.
author_facet Ott, Lauren R.
Penhale, Samantha H.
Taylor, Brittany K.
Lew, Brandon J.
Wang, Yu-Ping
Calhoun, Vince D.
Stephen, Julia M.
Wilson, Tony W.
author_sort Ott, Lauren R.
collection PubMed
description BACKGROUND: While numerous studies have examined the developmental trajectory of task-based neural oscillations during childhood and adolescence, far less is known about the evolution of spontaneous cortical activity during this time period. Likewise, many studies have shown robust sex differences in task-based oscillations during this developmental period, but whether such sex differences extend to spontaneous activity is not understood. METHODS: Herein, we examined spontaneous cortical activity in 111 typically-developing youth (ages 9–15 years; 55 male). Participants completed a resting state magnetoencephalographic (MEG) recording and a structural MRI. MEG data were source imaged and the power within five canonical frequency bands (delta, theta, alpha, beta, gamma) was computed. The resulting power spectral density maps were analyzed via vertex-wise ANCOVAs to identify spatially-specific effects of age, sex, and their interaction. RESULTS: We found robust increases in power with age in all frequencies except delta, which decreased over time, with findings largely confined to frontal cortices. Sex effects were distributed across frontal and temporal regions; females tended to have greater delta and beta power, whereas males had greater alpha. Importantly, there was a significant age-by-sex interaction in theta power, such that males exhibited decreasing power with age while females showed increasing power with age in the bilateral superior temporal cortices. DISCUSSION: These data suggest that the strength of spontaneous activity undergoes robust change during the transition from childhood to adolescence (i.e., puberty onset), with intriguing sex differences in some cortical areas. Future developmental studies should probe task-related oscillations and spontaneous activity in parallel.
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spelling pubmed-86857672021-12-20 Spontaneous cortical MEG activity undergoes unique age- and sex-related changes during the transition to adolescence Ott, Lauren R. Penhale, Samantha H. Taylor, Brittany K. Lew, Brandon J. Wang, Yu-Ping Calhoun, Vince D. Stephen, Julia M. Wilson, Tony W. Neuroimage Article BACKGROUND: While numerous studies have examined the developmental trajectory of task-based neural oscillations during childhood and adolescence, far less is known about the evolution of spontaneous cortical activity during this time period. Likewise, many studies have shown robust sex differences in task-based oscillations during this developmental period, but whether such sex differences extend to spontaneous activity is not understood. METHODS: Herein, we examined spontaneous cortical activity in 111 typically-developing youth (ages 9–15 years; 55 male). Participants completed a resting state magnetoencephalographic (MEG) recording and a structural MRI. MEG data were source imaged and the power within five canonical frequency bands (delta, theta, alpha, beta, gamma) was computed. The resulting power spectral density maps were analyzed via vertex-wise ANCOVAs to identify spatially-specific effects of age, sex, and their interaction. RESULTS: We found robust increases in power with age in all frequencies except delta, which decreased over time, with findings largely confined to frontal cortices. Sex effects were distributed across frontal and temporal regions; females tended to have greater delta and beta power, whereas males had greater alpha. Importantly, there was a significant age-by-sex interaction in theta power, such that males exhibited decreasing power with age while females showed increasing power with age in the bilateral superior temporal cortices. DISCUSSION: These data suggest that the strength of spontaneous activity undergoes robust change during the transition from childhood to adolescence (i.e., puberty onset), with intriguing sex differences in some cortical areas. Future developmental studies should probe task-related oscillations and spontaneous activity in parallel. 2021-09-10 2021-12-01 /pmc/articles/PMC8685767/ /pubmed/34517128 http://dx.doi.org/10.1016/j.neuroimage.2021.118552 Text en https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) )
spellingShingle Article
Ott, Lauren R.
Penhale, Samantha H.
Taylor, Brittany K.
Lew, Brandon J.
Wang, Yu-Ping
Calhoun, Vince D.
Stephen, Julia M.
Wilson, Tony W.
Spontaneous cortical MEG activity undergoes unique age- and sex-related changes during the transition to adolescence
title Spontaneous cortical MEG activity undergoes unique age- and sex-related changes during the transition to adolescence
title_full Spontaneous cortical MEG activity undergoes unique age- and sex-related changes during the transition to adolescence
title_fullStr Spontaneous cortical MEG activity undergoes unique age- and sex-related changes during the transition to adolescence
title_full_unstemmed Spontaneous cortical MEG activity undergoes unique age- and sex-related changes during the transition to adolescence
title_short Spontaneous cortical MEG activity undergoes unique age- and sex-related changes during the transition to adolescence
title_sort spontaneous cortical meg activity undergoes unique age- and sex-related changes during the transition to adolescence
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8685767/
https://www.ncbi.nlm.nih.gov/pubmed/34517128
http://dx.doi.org/10.1016/j.neuroimage.2021.118552
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