Cargando…

Age-associated changes in rich-club organisation in autistic and neurotypical human brains

Macroscopic structural networks in the human brain have a rich-club architecture comprising both highly inter-connected central regions and sparsely connected peripheral regions. Recent studies show that disruption of this functionally efficient organisation is associated with several psychiatric di...

Descripción completa

Detalles Bibliográficos
Autores principales: Watanabe, Takamitsu, Rees, Geraint
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4633620/
https://www.ncbi.nlm.nih.gov/pubmed/26537477
http://dx.doi.org/10.1038/srep16152
_version_ 1782399237031460864
author Watanabe, Takamitsu
Rees, Geraint
author_facet Watanabe, Takamitsu
Rees, Geraint
author_sort Watanabe, Takamitsu
collection PubMed
description Macroscopic structural networks in the human brain have a rich-club architecture comprising both highly inter-connected central regions and sparsely connected peripheral regions. Recent studies show that disruption of this functionally efficient organisation is associated with several psychiatric disorders. However, despite increasing attention to this network property, whether age-associated changes in rich-club organisation occur during human adolescence remains unclear. Here, analysing a publicly shared diffusion tensor imaging dataset, we found that, during adolescence, brains of typically developing (TD) individuals showed increases in rich-club organisation and inferred network functionality, whereas individuals with autism spectrum disorders (ASD) did not. These differences between TD and ASD groups were statistically significant for both structural and functional properties. Moreover, this typical age-related changes in rich-club organisation were characterised by progressive involvement of the right anterior insula. In contrast, in ASD individuals, did not show typical increases in grey matter volume, and this relative anatomical immaturity was correlated with the severity of ASD social symptoms. These results provide evidence that rich-club architecture is one of the bases of functionally efficient brain networks underpinning complex cognitive functions in adult human brains. Furthermore, our findings suggest that immature rich-club organisation might be associated with some neurodevelopmental disorders.
format Online
Article
Text
id pubmed-4633620
institution National Center for Biotechnology Information
language English
publishDate 2015
publisher Nature Publishing Group
record_format MEDLINE/PubMed
spelling pubmed-46336202015-11-05 Age-associated changes in rich-club organisation in autistic and neurotypical human brains Watanabe, Takamitsu Rees, Geraint Sci Rep Article Macroscopic structural networks in the human brain have a rich-club architecture comprising both highly inter-connected central regions and sparsely connected peripheral regions. Recent studies show that disruption of this functionally efficient organisation is associated with several psychiatric disorders. However, despite increasing attention to this network property, whether age-associated changes in rich-club organisation occur during human adolescence remains unclear. Here, analysing a publicly shared diffusion tensor imaging dataset, we found that, during adolescence, brains of typically developing (TD) individuals showed increases in rich-club organisation and inferred network functionality, whereas individuals with autism spectrum disorders (ASD) did not. These differences between TD and ASD groups were statistically significant for both structural and functional properties. Moreover, this typical age-related changes in rich-club organisation were characterised by progressive involvement of the right anterior insula. In contrast, in ASD individuals, did not show typical increases in grey matter volume, and this relative anatomical immaturity was correlated with the severity of ASD social symptoms. These results provide evidence that rich-club architecture is one of the bases of functionally efficient brain networks underpinning complex cognitive functions in adult human brains. Furthermore, our findings suggest that immature rich-club organisation might be associated with some neurodevelopmental disorders. Nature Publishing Group 2015-11-05 /pmc/articles/PMC4633620/ /pubmed/26537477 http://dx.doi.org/10.1038/srep16152 Text en Copyright © 2015, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Watanabe, Takamitsu
Rees, Geraint
Age-associated changes in rich-club organisation in autistic and neurotypical human brains
title Age-associated changes in rich-club organisation in autistic and neurotypical human brains
title_full Age-associated changes in rich-club organisation in autistic and neurotypical human brains
title_fullStr Age-associated changes in rich-club organisation in autistic and neurotypical human brains
title_full_unstemmed Age-associated changes in rich-club organisation in autistic and neurotypical human brains
title_short Age-associated changes in rich-club organisation in autistic and neurotypical human brains
title_sort age-associated changes in rich-club organisation in autistic and neurotypical human brains
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4633620/
https://www.ncbi.nlm.nih.gov/pubmed/26537477
http://dx.doi.org/10.1038/srep16152
work_keys_str_mv AT watanabetakamitsu ageassociatedchangesinrichcluborganisationinautisticandneurotypicalhumanbrains
AT reesgeraint ageassociatedchangesinrichcluborganisationinautisticandneurotypicalhumanbrains