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Topographical relocation of adolescent sleep spindles reveals a new maturational pattern in the human brain
Current theories of human neural development emphasize the posterior-to-anterior pattern of brain maturation. However, this scenario leaves out significant brain areas not directly involved with sensory input and behavioral control. Suggesting the relevance of cortical activity unrelated to sensory...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9054798/ https://www.ncbi.nlm.nih.gov/pubmed/35487959 http://dx.doi.org/10.1038/s41598-022-11098-8 |
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author | Gombos, Ferenc Bódizs, Róbert Pótári, Adrián Bocskai, Gábor Berencsi, Andrea Szakács, Hanna Kovács, Ilona |
author_facet | Gombos, Ferenc Bódizs, Róbert Pótári, Adrián Bocskai, Gábor Berencsi, Andrea Szakács, Hanna Kovács, Ilona |
author_sort | Gombos, Ferenc |
collection | PubMed |
description | Current theories of human neural development emphasize the posterior-to-anterior pattern of brain maturation. However, this scenario leaves out significant brain areas not directly involved with sensory input and behavioral control. Suggesting the relevance of cortical activity unrelated to sensory stimulation, such as sleep, we investigated adolescent transformations in the topography of sleep spindles. Sleep spindles are known to be involved in neural plasticity and in adults have a bimodal topography: slow spindles are frontally dominant, while fast spindles have a parietal/precuneal origin. The late functional segregation of the precuneus from the frontoparietal network during adolescence suggests that spindle topography might approach the adult state relatively late in development, and it may not be a result of the posterior-to-anterior maturational pattern. We analyzed the topographical distribution of spindle parameters in HD-EEG polysomnographic sleep recordings of adolescents and found that slow spindle duration maxima traveled from central to anterior brain regions, while fast spindle density, amplitude and frequency peaks traveled from central to more posterior brain regions. These results provide evidence for the gradual posteriorization of the anatomical localization of fast sleep spindles during adolescence and indicate the existence of an anterior-to-posterior pattern of human brain maturation. |
format | Online Article Text |
id | pubmed-9054798 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-90547982022-05-01 Topographical relocation of adolescent sleep spindles reveals a new maturational pattern in the human brain Gombos, Ferenc Bódizs, Róbert Pótári, Adrián Bocskai, Gábor Berencsi, Andrea Szakács, Hanna Kovács, Ilona Sci Rep Article Current theories of human neural development emphasize the posterior-to-anterior pattern of brain maturation. However, this scenario leaves out significant brain areas not directly involved with sensory input and behavioral control. Suggesting the relevance of cortical activity unrelated to sensory stimulation, such as sleep, we investigated adolescent transformations in the topography of sleep spindles. Sleep spindles are known to be involved in neural plasticity and in adults have a bimodal topography: slow spindles are frontally dominant, while fast spindles have a parietal/precuneal origin. The late functional segregation of the precuneus from the frontoparietal network during adolescence suggests that spindle topography might approach the adult state relatively late in development, and it may not be a result of the posterior-to-anterior maturational pattern. We analyzed the topographical distribution of spindle parameters in HD-EEG polysomnographic sleep recordings of adolescents and found that slow spindle duration maxima traveled from central to anterior brain regions, while fast spindle density, amplitude and frequency peaks traveled from central to more posterior brain regions. These results provide evidence for the gradual posteriorization of the anatomical localization of fast sleep spindles during adolescence and indicate the existence of an anterior-to-posterior pattern of human brain maturation. Nature Publishing Group UK 2022-04-29 /pmc/articles/PMC9054798/ /pubmed/35487959 http://dx.doi.org/10.1038/s41598-022-11098-8 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Gombos, Ferenc Bódizs, Róbert Pótári, Adrián Bocskai, Gábor Berencsi, Andrea Szakács, Hanna Kovács, Ilona Topographical relocation of adolescent sleep spindles reveals a new maturational pattern in the human brain |
title | Topographical relocation of adolescent sleep spindles reveals a new maturational pattern in the human brain |
title_full | Topographical relocation of adolescent sleep spindles reveals a new maturational pattern in the human brain |
title_fullStr | Topographical relocation of adolescent sleep spindles reveals a new maturational pattern in the human brain |
title_full_unstemmed | Topographical relocation of adolescent sleep spindles reveals a new maturational pattern in the human brain |
title_short | Topographical relocation of adolescent sleep spindles reveals a new maturational pattern in the human brain |
title_sort | topographical relocation of adolescent sleep spindles reveals a new maturational pattern in the human brain |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9054798/ https://www.ncbi.nlm.nih.gov/pubmed/35487959 http://dx.doi.org/10.1038/s41598-022-11098-8 |
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