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Aberrant age-related alterations in spontaneous cortical activity in participants with cerebral palsy

INTRODUCTION: Cerebral Palsy (CP) is the most common neurodevelopmental motor disability, resulting in life-long sensory, perception and motor impairments. Moreover, these impairments appear to drastically worsen as the population with CP transitions from adolescents to adulthood, although the under...

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Autores principales: Bergwell, Hannah, Trevarrow, Michael P., Heinrichs-Graham, Elizabeth, Reelfs, Anna, Ott, Lauren R., Penhale, Samantha H., Wilson, Tony W., Kurz, Max J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10374009/
https://www.ncbi.nlm.nih.gov/pubmed/37521295
http://dx.doi.org/10.3389/fneur.2023.1163964
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author Bergwell, Hannah
Trevarrow, Michael P.
Heinrichs-Graham, Elizabeth
Reelfs, Anna
Ott, Lauren R.
Penhale, Samantha H.
Wilson, Tony W.
Kurz, Max J.
author_facet Bergwell, Hannah
Trevarrow, Michael P.
Heinrichs-Graham, Elizabeth
Reelfs, Anna
Ott, Lauren R.
Penhale, Samantha H.
Wilson, Tony W.
Kurz, Max J.
author_sort Bergwell, Hannah
collection PubMed
description INTRODUCTION: Cerebral Palsy (CP) is the most common neurodevelopmental motor disability, resulting in life-long sensory, perception and motor impairments. Moreover, these impairments appear to drastically worsen as the population with CP transitions from adolescents to adulthood, although the underlying neurophysiological mechanisms remain poorly understood. METHODS: We began to address this knowledge gap by utilizing magnetoencephalographic (MEG) brain imaging to study how the amplitude of spontaneous cortical activity (i.e., resting state) is altered during this transition period in a cohort of 38 individuals with spastic diplegic CP (Age range = 9.80–47.50 years, 20 females) and 67 neurotypical controls (NT) (Age range = 9.08–49.40 years, Females = 27). MEG data from a five-minute eyes closed resting-state paradigm were source imaged, and the power within the delta (2–4 Hz), theta (5–7 Hz), alpha (8–12 Hz), beta (15–29 Hz), and gamma (30–59 Hz) frequency bands were computed. RESULTS: For both groups, the delta and theta spontaneous power decreased in the bilateral temporoparietal and superior parietal regions with age, while alpha, beta, and gamma band spontaneous power increased in temporoparietal, frontoparietal and premotor regions with age. We also found a significant group x age interaction, such that participants with CP demonstrated significantly less age-related increases in the spontaneous beta activity in the bilateral sensorimotor cortices compared to NT controls. DISCUSSION: Overall, these results demonstrate that the spontaneous neural activity in individuals with CP has an altered trajectory when transitioning from adolescents to adulthood. We suggest that these differences in spontaneous cortical activity may play a critical role in the aberrant motor actions seen in this patient group, and may provide a neurophysiological marker for assessing the effectiveness of current treatment strategies that are directed at improving the mobility and sensorimotor impairments seen in individuals with CP.
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spelling pubmed-103740092023-07-28 Aberrant age-related alterations in spontaneous cortical activity in participants with cerebral palsy Bergwell, Hannah Trevarrow, Michael P. Heinrichs-Graham, Elizabeth Reelfs, Anna Ott, Lauren R. Penhale, Samantha H. Wilson, Tony W. Kurz, Max J. Front Neurol Neurology INTRODUCTION: Cerebral Palsy (CP) is the most common neurodevelopmental motor disability, resulting in life-long sensory, perception and motor impairments. Moreover, these impairments appear to drastically worsen as the population with CP transitions from adolescents to adulthood, although the underlying neurophysiological mechanisms remain poorly understood. METHODS: We began to address this knowledge gap by utilizing magnetoencephalographic (MEG) brain imaging to study how the amplitude of spontaneous cortical activity (i.e., resting state) is altered during this transition period in a cohort of 38 individuals with spastic diplegic CP (Age range = 9.80–47.50 years, 20 females) and 67 neurotypical controls (NT) (Age range = 9.08–49.40 years, Females = 27). MEG data from a five-minute eyes closed resting-state paradigm were source imaged, and the power within the delta (2–4 Hz), theta (5–7 Hz), alpha (8–12 Hz), beta (15–29 Hz), and gamma (30–59 Hz) frequency bands were computed. RESULTS: For both groups, the delta and theta spontaneous power decreased in the bilateral temporoparietal and superior parietal regions with age, while alpha, beta, and gamma band spontaneous power increased in temporoparietal, frontoparietal and premotor regions with age. We also found a significant group x age interaction, such that participants with CP demonstrated significantly less age-related increases in the spontaneous beta activity in the bilateral sensorimotor cortices compared to NT controls. DISCUSSION: Overall, these results demonstrate that the spontaneous neural activity in individuals with CP has an altered trajectory when transitioning from adolescents to adulthood. We suggest that these differences in spontaneous cortical activity may play a critical role in the aberrant motor actions seen in this patient group, and may provide a neurophysiological marker for assessing the effectiveness of current treatment strategies that are directed at improving the mobility and sensorimotor impairments seen in individuals with CP. Frontiers Media S.A. 2023-07-13 /pmc/articles/PMC10374009/ /pubmed/37521295 http://dx.doi.org/10.3389/fneur.2023.1163964 Text en Copyright © 2023 Bergwell, Trevarrow, Heinrichs-Graham, Reelfs, Ott, Penhale, Wilson and Kurz. https://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 Neurology
Bergwell, Hannah
Trevarrow, Michael P.
Heinrichs-Graham, Elizabeth
Reelfs, Anna
Ott, Lauren R.
Penhale, Samantha H.
Wilson, Tony W.
Kurz, Max J.
Aberrant age-related alterations in spontaneous cortical activity in participants with cerebral palsy
title Aberrant age-related alterations in spontaneous cortical activity in participants with cerebral palsy
title_full Aberrant age-related alterations in spontaneous cortical activity in participants with cerebral palsy
title_fullStr Aberrant age-related alterations in spontaneous cortical activity in participants with cerebral palsy
title_full_unstemmed Aberrant age-related alterations in spontaneous cortical activity in participants with cerebral palsy
title_short Aberrant age-related alterations in spontaneous cortical activity in participants with cerebral palsy
title_sort aberrant age-related alterations in spontaneous cortical activity in participants with cerebral palsy
topic Neurology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10374009/
https://www.ncbi.nlm.nih.gov/pubmed/37521295
http://dx.doi.org/10.3389/fneur.2023.1163964
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