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The development of sensorimotor cortical oscillations is mediated by pubertal testosterone

Puberty is a period of substantial hormonal fluctuations, and pubertal hormones can modulate structural and functional changes in the developing brain. Many previous studies have characterized the neural oscillatory responses serving movement, which include a beta event-related desynchronization (ER...

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Autores principales: Fung, Madison H., Heinrichs-Graham, Elizabeth, Taylor, Brittany K., Frenzel, Michaela R., Eastman, Jacob A., Wang, Yu-Ping, Calhoun, Vince D., Stephen, Julia M., Wilson, Tony W.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9816764/
https://www.ncbi.nlm.nih.gov/pubmed/36368502
http://dx.doi.org/10.1016/j.neuroimage.2022.119745
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author Fung, Madison H.
Heinrichs-Graham, Elizabeth
Taylor, Brittany K.
Frenzel, Michaela R.
Eastman, Jacob A.
Wang, Yu-Ping
Calhoun, Vince D.
Stephen, Julia M.
Wilson, Tony W.
author_facet Fung, Madison H.
Heinrichs-Graham, Elizabeth
Taylor, Brittany K.
Frenzel, Michaela R.
Eastman, Jacob A.
Wang, Yu-Ping
Calhoun, Vince D.
Stephen, Julia M.
Wilson, Tony W.
author_sort Fung, Madison H.
collection PubMed
description Puberty is a period of substantial hormonal fluctuations, and pubertal hormones can modulate structural and functional changes in the developing brain. Many previous studies have characterized the neural oscillatory responses serving movement, which include a beta event-related desynchronization (ERD) preceding movement onset, gamma and theta responses coinciding with movement execution, and a post-movement beta-rebound (PMBR) response following movement offset. While a few studies have investigated the developmental trajectories of these neural oscillations serving motor control, the impact of pubertal hormone levels on the maturation of these dynamics has not yet been examined. Since the timing and tempo of puberty varies greatly between individuals, pubertal hormones may uniquely impact the maturation of motor cortical oscillations distinct from other developmental metrics, such as age. In the current study we quantified these oscillations using magnetoencephalography (MEG) and utilized chronological age and measures of endogenous testosterone as indices of development during the transition from childhood to adolescence in 69 youths. Mediation analyses revealed complex maturation patterns for the beta ERD, in which testosterone predicted both spontaneous baseline and ERD power through direct and indirect effects. Age, but not pubertal hormones, predicted motor-related theta, and no relationships between oscillatory responses and developmental metrics were found for gamma or PMBR responses. These findings provide novel insight into how pubertal hormones affect motor-related oscillations, and highlight the continued development of motor cortical dynamics throughout the pubertal period.
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spelling pubmed-98167642023-01-06 The development of sensorimotor cortical oscillations is mediated by pubertal testosterone Fung, Madison H. Heinrichs-Graham, Elizabeth Taylor, Brittany K. Frenzel, Michaela R. Eastman, Jacob A. Wang, Yu-Ping Calhoun, Vince D. Stephen, Julia M. Wilson, Tony W. Neuroimage Article Puberty is a period of substantial hormonal fluctuations, and pubertal hormones can modulate structural and functional changes in the developing brain. Many previous studies have characterized the neural oscillatory responses serving movement, which include a beta event-related desynchronization (ERD) preceding movement onset, gamma and theta responses coinciding with movement execution, and a post-movement beta-rebound (PMBR) response following movement offset. While a few studies have investigated the developmental trajectories of these neural oscillations serving motor control, the impact of pubertal hormone levels on the maturation of these dynamics has not yet been examined. Since the timing and tempo of puberty varies greatly between individuals, pubertal hormones may uniquely impact the maturation of motor cortical oscillations distinct from other developmental metrics, such as age. In the current study we quantified these oscillations using magnetoencephalography (MEG) and utilized chronological age and measures of endogenous testosterone as indices of development during the transition from childhood to adolescence in 69 youths. Mediation analyses revealed complex maturation patterns for the beta ERD, in which testosterone predicted both spontaneous baseline and ERD power through direct and indirect effects. Age, but not pubertal hormones, predicted motor-related theta, and no relationships between oscillatory responses and developmental metrics were found for gamma or PMBR responses. These findings provide novel insight into how pubertal hormones affect motor-related oscillations, and highlight the continued development of motor cortical dynamics throughout the pubertal period. 2022-12-01 2022-11-09 /pmc/articles/PMC9816764/ /pubmed/36368502 http://dx.doi.org/10.1016/j.neuroimage.2022.119745 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
Fung, Madison H.
Heinrichs-Graham, Elizabeth
Taylor, Brittany K.
Frenzel, Michaela R.
Eastman, Jacob A.
Wang, Yu-Ping
Calhoun, Vince D.
Stephen, Julia M.
Wilson, Tony W.
The development of sensorimotor cortical oscillations is mediated by pubertal testosterone
title The development of sensorimotor cortical oscillations is mediated by pubertal testosterone
title_full The development of sensorimotor cortical oscillations is mediated by pubertal testosterone
title_fullStr The development of sensorimotor cortical oscillations is mediated by pubertal testosterone
title_full_unstemmed The development of sensorimotor cortical oscillations is mediated by pubertal testosterone
title_short The development of sensorimotor cortical oscillations is mediated by pubertal testosterone
title_sort development of sensorimotor cortical oscillations is mediated by pubertal testosterone
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9816764/
https://www.ncbi.nlm.nih.gov/pubmed/36368502
http://dx.doi.org/10.1016/j.neuroimage.2022.119745
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