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Developmental white matter microstructure in autism phenotype and corresponding endophenotype during adolescence

During adolescence, white matter microstructure undergoes an important stage of development. It is hypothesized that the alterations of brain connectivity that have a key role in autism spectrum conditions (ASCs) may interact with the development of white matter microstructure. This interaction may...

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Autores principales: Lisiecka, D M, Holt, R, Tait, R, Ford, M, Lai, M-C, Chura, L R, Baron-Cohen, S, Spencer, M D, Suckling, J
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4354353/
https://www.ncbi.nlm.nih.gov/pubmed/25781228
http://dx.doi.org/10.1038/tp.2015.23
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author Lisiecka, D M
Holt, R
Tait, R
Ford, M
Lai, M-C
Chura, L R
Baron-Cohen, S
Spencer, M D
Suckling, J
author_facet Lisiecka, D M
Holt, R
Tait, R
Ford, M
Lai, M-C
Chura, L R
Baron-Cohen, S
Spencer, M D
Suckling, J
author_sort Lisiecka, D M
collection PubMed
description During adolescence, white matter microstructure undergoes an important stage of development. It is hypothesized that the alterations of brain connectivity that have a key role in autism spectrum conditions (ASCs) may interact with the development of white matter microstructure. This interaction may be present beyond the phenotype of autism in siblings of individuals with ASC, who are 10 to 20 times more likely to develop certain forms of ASC. We use diffusion tensor imaging to examine how white matter microstructure measurements correlate with age in typically developing individuals, and how this correlation differs in n=43 adolescents with ASC and their n=38 siblings. Correlations observed in n=40 typically developing individuals match developmental changes noted in previous longitudinal studies. In comparison, individuals with ASC display weaker negative correlation between age and mean diffusivity in a broad area centred in the right superior longitudinal fasciculus. These differences may be caused either by increased heterogeneity in ASC or by temporal alterations in the group's developmental pattern. Siblings of individuals with ASC also show diminished negative correlation between age and one component of mean diffusivity—second diffusion eigenvalue—in the right superior longitudinal fasciculus. As the observed differences match for location and correlation directionality in our comparison of typically developing individuals to those with ASC and their siblings, we propose that these alterations constitute a part of the endophenotype of autism.
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spelling pubmed-43543532015-03-12 Developmental white matter microstructure in autism phenotype and corresponding endophenotype during adolescence Lisiecka, D M Holt, R Tait, R Ford, M Lai, M-C Chura, L R Baron-Cohen, S Spencer, M D Suckling, J Transl Psychiatry Original Article During adolescence, white matter microstructure undergoes an important stage of development. It is hypothesized that the alterations of brain connectivity that have a key role in autism spectrum conditions (ASCs) may interact with the development of white matter microstructure. This interaction may be present beyond the phenotype of autism in siblings of individuals with ASC, who are 10 to 20 times more likely to develop certain forms of ASC. We use diffusion tensor imaging to examine how white matter microstructure measurements correlate with age in typically developing individuals, and how this correlation differs in n=43 adolescents with ASC and their n=38 siblings. Correlations observed in n=40 typically developing individuals match developmental changes noted in previous longitudinal studies. In comparison, individuals with ASC display weaker negative correlation between age and mean diffusivity in a broad area centred in the right superior longitudinal fasciculus. These differences may be caused either by increased heterogeneity in ASC or by temporal alterations in the group's developmental pattern. Siblings of individuals with ASC also show diminished negative correlation between age and one component of mean diffusivity—second diffusion eigenvalue—in the right superior longitudinal fasciculus. As the observed differences match for location and correlation directionality in our comparison of typically developing individuals to those with ASC and their siblings, we propose that these alterations constitute a part of the endophenotype of autism. Nature Publishing Group 2015-03 2015-03-17 /pmc/articles/PMC4354353/ /pubmed/25781228 http://dx.doi.org/10.1038/tp.2015.23 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 Original Article
Lisiecka, D M
Holt, R
Tait, R
Ford, M
Lai, M-C
Chura, L R
Baron-Cohen, S
Spencer, M D
Suckling, J
Developmental white matter microstructure in autism phenotype and corresponding endophenotype during adolescence
title Developmental white matter microstructure in autism phenotype and corresponding endophenotype during adolescence
title_full Developmental white matter microstructure in autism phenotype and corresponding endophenotype during adolescence
title_fullStr Developmental white matter microstructure in autism phenotype and corresponding endophenotype during adolescence
title_full_unstemmed Developmental white matter microstructure in autism phenotype and corresponding endophenotype during adolescence
title_short Developmental white matter microstructure in autism phenotype and corresponding endophenotype during adolescence
title_sort developmental white matter microstructure in autism phenotype and corresponding endophenotype during adolescence
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4354353/
https://www.ncbi.nlm.nih.gov/pubmed/25781228
http://dx.doi.org/10.1038/tp.2015.23
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