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Ageing‐related changes in nap neuroscillatory activity are mediated and moderated by grey matter volume

Ageing‐related changes in grey matter result in changes in the intensity and topography of sleep neural activity. However, it is unclear whether these findings can be explained by ageing‐related differences in sleep pressure or circadian influence. The current study used high‐density electroencephal...

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Autores principales: Fitzroy, Ahren B., Kainec, Kyle A., Spencer, Rebecca M. C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8809479/
https://www.ncbi.nlm.nih.gov/pubmed/34541728
http://dx.doi.org/10.1111/ejn.15468
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author Fitzroy, Ahren B.
Kainec, Kyle A.
Spencer, Rebecca M. C.
author_facet Fitzroy, Ahren B.
Kainec, Kyle A.
Spencer, Rebecca M. C.
author_sort Fitzroy, Ahren B.
collection PubMed
description Ageing‐related changes in grey matter result in changes in the intensity and topography of sleep neural activity. However, it is unclear whether these findings can be explained by ageing‐related differences in sleep pressure or circadian influence. The current study used high‐density electroencephalography to assess how grey matter volume differences between young and older adults mediate and moderate neuroscillatory activity differences during a midday nap following a motor sequencing task. Delta, theta, and sigma amplitude were reduced in older relative to young adults, especially over frontocentral scalp, leading to increases in relative delta frontality and relative sigma lateral centroposteriority. Delta reductions in older adults were mediated by grey matter loss in frontal medial cortex, primary motor cortex, thalamus, caudate, putamen, and pallidum, and were moderated by putamen grey matter volume. Theta reductions were mediated by grey matter loss in primary motor cortex, thalamus, and caudate, and were moderated by putamen and pallidum grey matter volume. Sigma changes were moderated by putamen and pallidum grey matter volume. Moderation results suggested that across frequencies, young adults with more grey matter had increased activity, whereas older adults with more grey matter had unchanged or decreased activity. These results provide a critical extension of previous findings from overnight sleep in a midday nap, indicating that they are not driven by sleep pressure or circadian confounds. Moreover, these results suggest brain regions associated with motor sequence learning contribute to sleep neural activity following a motor sequencing task.
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spelling pubmed-88094792022-10-14 Ageing‐related changes in nap neuroscillatory activity are mediated and moderated by grey matter volume Fitzroy, Ahren B. Kainec, Kyle A. Spencer, Rebecca M. C. Eur J Neurosci Clinical and Translational Neuroscience Ageing‐related changes in grey matter result in changes in the intensity and topography of sleep neural activity. However, it is unclear whether these findings can be explained by ageing‐related differences in sleep pressure or circadian influence. The current study used high‐density electroencephalography to assess how grey matter volume differences between young and older adults mediate and moderate neuroscillatory activity differences during a midday nap following a motor sequencing task. Delta, theta, and sigma amplitude were reduced in older relative to young adults, especially over frontocentral scalp, leading to increases in relative delta frontality and relative sigma lateral centroposteriority. Delta reductions in older adults were mediated by grey matter loss in frontal medial cortex, primary motor cortex, thalamus, caudate, putamen, and pallidum, and were moderated by putamen grey matter volume. Theta reductions were mediated by grey matter loss in primary motor cortex, thalamus, and caudate, and were moderated by putamen and pallidum grey matter volume. Sigma changes were moderated by putamen and pallidum grey matter volume. Moderation results suggested that across frequencies, young adults with more grey matter had increased activity, whereas older adults with more grey matter had unchanged or decreased activity. These results provide a critical extension of previous findings from overnight sleep in a midday nap, indicating that they are not driven by sleep pressure or circadian confounds. Moreover, these results suggest brain regions associated with motor sequence learning contribute to sleep neural activity following a motor sequencing task. John Wiley and Sons Inc. 2021-10-05 2021-11 /pmc/articles/PMC8809479/ /pubmed/34541728 http://dx.doi.org/10.1111/ejn.15468 Text en © 2021 The Authors. European Journal of Neuroscience published by Federation of European Neuroscience Societies and John Wiley & Sons Ltd. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Clinical and Translational Neuroscience
Fitzroy, Ahren B.
Kainec, Kyle A.
Spencer, Rebecca M. C.
Ageing‐related changes in nap neuroscillatory activity are mediated and moderated by grey matter volume
title Ageing‐related changes in nap neuroscillatory activity are mediated and moderated by grey matter volume
title_full Ageing‐related changes in nap neuroscillatory activity are mediated and moderated by grey matter volume
title_fullStr Ageing‐related changes in nap neuroscillatory activity are mediated and moderated by grey matter volume
title_full_unstemmed Ageing‐related changes in nap neuroscillatory activity are mediated and moderated by grey matter volume
title_short Ageing‐related changes in nap neuroscillatory activity are mediated and moderated by grey matter volume
title_sort ageing‐related changes in nap neuroscillatory activity are mediated and moderated by grey matter volume
topic Clinical and Translational Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8809479/
https://www.ncbi.nlm.nih.gov/pubmed/34541728
http://dx.doi.org/10.1111/ejn.15468
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