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Functional EEG connectivity in infants associates with later restricted and repetitive behaviours in autism; a replication study

We conducted a replication study of our prior report that increased alpha EEG connectivity at 14-months associates with later autism spectrum disorder (ASD) diagnosis, and dimensional variation in restricted interests/repetitive behaviours. 143 infants at high and low familial risk for ASD watched d...

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Autores principales: Haartsen, Rianne, Jones, Emily J. H., Orekhova, Elena V., Charman, Tony, Johnson, Mark H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6361892/
https://www.ncbi.nlm.nih.gov/pubmed/30718487
http://dx.doi.org/10.1038/s41398-019-0380-2
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author Haartsen, Rianne
Jones, Emily J. H.
Orekhova, Elena V.
Charman, Tony
Johnson, Mark H.
author_facet Haartsen, Rianne
Jones, Emily J. H.
Orekhova, Elena V.
Charman, Tony
Johnson, Mark H.
author_sort Haartsen, Rianne
collection PubMed
description We conducted a replication study of our prior report that increased alpha EEG connectivity at 14-months associates with later autism spectrum disorder (ASD) diagnosis, and dimensional variation in restricted interests/repetitive behaviours. 143 infants at high and low familial risk for ASD watched dynamic videos of spinning toys and women singing nursery rhymes while high-density EEG was recorded. Alpha functional connectivity (7–8 Hz) was calculated using the debiased weighted phase lag index. The final sample with clean data included low-risk infants (N = 20), and high-risk infants who at 36 months showed either typical development (N = 47), atypical development (N = 21), or met criteria for ASD (N = 13). While we did not replicate the finding that global EEG connectivity associated with ASD diagnosis, we did replicate the association between higher functional connectivity at 14 months and greater severity of restricted and repetitive behaviours at 36 months in infants who met criteria for ASD. We further showed that this association is strongest for the circumscribed interests subdomain. We propose that structural and/or functional abnormalities in frontal-striatal circuits underlie the observed association. This is the first replicated infant neural predictor of dimensional variation in later ASD symptoms.
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spelling pubmed-63618922019-02-06 Functional EEG connectivity in infants associates with later restricted and repetitive behaviours in autism; a replication study Haartsen, Rianne Jones, Emily J. H. Orekhova, Elena V. Charman, Tony Johnson, Mark H. Transl Psychiatry Article We conducted a replication study of our prior report that increased alpha EEG connectivity at 14-months associates with later autism spectrum disorder (ASD) diagnosis, and dimensional variation in restricted interests/repetitive behaviours. 143 infants at high and low familial risk for ASD watched dynamic videos of spinning toys and women singing nursery rhymes while high-density EEG was recorded. Alpha functional connectivity (7–8 Hz) was calculated using the debiased weighted phase lag index. The final sample with clean data included low-risk infants (N = 20), and high-risk infants who at 36 months showed either typical development (N = 47), atypical development (N = 21), or met criteria for ASD (N = 13). While we did not replicate the finding that global EEG connectivity associated with ASD diagnosis, we did replicate the association between higher functional connectivity at 14 months and greater severity of restricted and repetitive behaviours at 36 months in infants who met criteria for ASD. We further showed that this association is strongest for the circumscribed interests subdomain. We propose that structural and/or functional abnormalities in frontal-striatal circuits underlie the observed association. This is the first replicated infant neural predictor of dimensional variation in later ASD symptoms. Nature Publishing Group UK 2019-02-04 /pmc/articles/PMC6361892/ /pubmed/30718487 http://dx.doi.org/10.1038/s41398-019-0380-2 Text en © The Author(s) 2019 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Haartsen, Rianne
Jones, Emily J. H.
Orekhova, Elena V.
Charman, Tony
Johnson, Mark H.
Functional EEG connectivity in infants associates with later restricted and repetitive behaviours in autism; a replication study
title Functional EEG connectivity in infants associates with later restricted and repetitive behaviours in autism; a replication study
title_full Functional EEG connectivity in infants associates with later restricted and repetitive behaviours in autism; a replication study
title_fullStr Functional EEG connectivity in infants associates with later restricted and repetitive behaviours in autism; a replication study
title_full_unstemmed Functional EEG connectivity in infants associates with later restricted and repetitive behaviours in autism; a replication study
title_short Functional EEG connectivity in infants associates with later restricted and repetitive behaviours in autism; a replication study
title_sort functional eeg connectivity in infants associates with later restricted and repetitive behaviours in autism; a replication study
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6361892/
https://www.ncbi.nlm.nih.gov/pubmed/30718487
http://dx.doi.org/10.1038/s41398-019-0380-2
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