Cargando…
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...
Autores principales: | , , , , , , , |
---|---|
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 |
_version_ | 1784617885702815744 |
---|---|
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. |
format | Online Article Text |
id | pubmed-8685767 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT ottlaurenr spontaneouscorticalmegactivityundergoesuniqueageandsexrelatedchangesduringthetransitiontoadolescence AT penhalesamanthah spontaneouscorticalmegactivityundergoesuniqueageandsexrelatedchangesduringthetransitiontoadolescence AT taylorbrittanyk spontaneouscorticalmegactivityundergoesuniqueageandsexrelatedchangesduringthetransitiontoadolescence AT lewbrandonj spontaneouscorticalmegactivityundergoesuniqueageandsexrelatedchangesduringthetransitiontoadolescence AT wangyuping spontaneouscorticalmegactivityundergoesuniqueageandsexrelatedchangesduringthetransitiontoadolescence AT calhounvinced spontaneouscorticalmegactivityundergoesuniqueageandsexrelatedchangesduringthetransitiontoadolescence AT stephenjuliam spontaneouscorticalmegactivityundergoesuniqueageandsexrelatedchangesduringthetransitiontoadolescence AT wilsontonyw spontaneouscorticalmegactivityundergoesuniqueageandsexrelatedchangesduringthetransitiontoadolescence |