Cargando…

Novel insights into axon diameter and myelin content in late childhood and adolescence

White matter microstructural development in late childhood and adolescence is driven predominantly by increasing axon density and myelin thickness. Ex vivo studies suggest that the increase in axon diameter drives developmental increases in axon density observed with pubertal onset. In this cross-se...

Descripción completa

Detalles Bibliográficos
Autores principales: Genc, Sila, Raven, Erika P, Drakesmith, Mark, Blakemore, Sarah-Jayne, Jones, Derek K
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10183755/
https://www.ncbi.nlm.nih.gov/pubmed/36610731
http://dx.doi.org/10.1093/cercor/bhac515
_version_ 1785042022682329088
author Genc, Sila
Raven, Erika P
Drakesmith, Mark
Blakemore, Sarah-Jayne
Jones, Derek K
author_facet Genc, Sila
Raven, Erika P
Drakesmith, Mark
Blakemore, Sarah-Jayne
Jones, Derek K
author_sort Genc, Sila
collection PubMed
description White matter microstructural development in late childhood and adolescence is driven predominantly by increasing axon density and myelin thickness. Ex vivo studies suggest that the increase in axon diameter drives developmental increases in axon density observed with pubertal onset. In this cross-sectional study, 50 typically developing participants aged 8–18 years were scanned using an ultra-strong gradient magnetic resonance imaging scanner. Microstructural properties, including apparent axon diameter [Formula: see text] , myelin content, and g-ratio, were estimated in regions of the corpus callosum. We observed age-related differences in [Formula: see text] , myelin content, and g-ratio. In early puberty, males had larger [Formula: see text] in the splenium and lower myelin content in the genu and body of the corpus callosum, compared with females. Overall, this work provides novel insights into developmental, pubertal, and cognitive correlates of individual differences in apparent axon diameter and myelin content in the developing human brain.
format Online
Article
Text
id pubmed-10183755
institution National Center for Biotechnology Information
language English
publishDate 2023
publisher Oxford University Press
record_format MEDLINE/PubMed
spelling pubmed-101837552023-05-16 Novel insights into axon diameter and myelin content in late childhood and adolescence Genc, Sila Raven, Erika P Drakesmith, Mark Blakemore, Sarah-Jayne Jones, Derek K Cereb Cortex Original Article White matter microstructural development in late childhood and adolescence is driven predominantly by increasing axon density and myelin thickness. Ex vivo studies suggest that the increase in axon diameter drives developmental increases in axon density observed with pubertal onset. In this cross-sectional study, 50 typically developing participants aged 8–18 years were scanned using an ultra-strong gradient magnetic resonance imaging scanner. Microstructural properties, including apparent axon diameter [Formula: see text] , myelin content, and g-ratio, were estimated in regions of the corpus callosum. We observed age-related differences in [Formula: see text] , myelin content, and g-ratio. In early puberty, males had larger [Formula: see text] in the splenium and lower myelin content in the genu and body of the corpus callosum, compared with females. Overall, this work provides novel insights into developmental, pubertal, and cognitive correlates of individual differences in apparent axon diameter and myelin content in the developing human brain. Oxford University Press 2023-01-04 /pmc/articles/PMC10183755/ /pubmed/36610731 http://dx.doi.org/10.1093/cercor/bhac515 Text en © The Author(s) 2023. Published by Oxford University Press. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Genc, Sila
Raven, Erika P
Drakesmith, Mark
Blakemore, Sarah-Jayne
Jones, Derek K
Novel insights into axon diameter and myelin content in late childhood and adolescence
title Novel insights into axon diameter and myelin content in late childhood and adolescence
title_full Novel insights into axon diameter and myelin content in late childhood and adolescence
title_fullStr Novel insights into axon diameter and myelin content in late childhood and adolescence
title_full_unstemmed Novel insights into axon diameter and myelin content in late childhood and adolescence
title_short Novel insights into axon diameter and myelin content in late childhood and adolescence
title_sort novel insights into axon diameter and myelin content in late childhood and adolescence
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10183755/
https://www.ncbi.nlm.nih.gov/pubmed/36610731
http://dx.doi.org/10.1093/cercor/bhac515
work_keys_str_mv AT gencsila novelinsightsintoaxondiameterandmyelincontentinlatechildhoodandadolescence
AT ravenerikap novelinsightsintoaxondiameterandmyelincontentinlatechildhoodandadolescence
AT drakesmithmark novelinsightsintoaxondiameterandmyelincontentinlatechildhoodandadolescence
AT blakemoresarahjayne novelinsightsintoaxondiameterandmyelincontentinlatechildhoodandadolescence
AT jonesderekk novelinsightsintoaxondiameterandmyelincontentinlatechildhoodandadolescence