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Structural and functional brain abnormalities in children with schizotypal disorder: a pilot study

Schizotypal disorder lies in the schizophrenia spectrum and is widely studied in adult populations. Schizotypal disorder in children (SDc) is less well described. This study examined brain morphological and functional connectivity abnormalities in SDc (12 SDc and 9 typically developing children), fo...

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Autores principales: Wang, Ya, Harding, Ian H., Testa, Renee, Tonge, Bruce, Jones, Harvey, Seal, Marc, Ross, Nola, Chan, Raymond C. K., van Beurden, Florian, Abu-Akel, Ahmad, Skafidas, Efstratios, Pantelis, Christos
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7080771/
https://www.ncbi.nlm.nih.gov/pubmed/32188859
http://dx.doi.org/10.1038/s41537-020-0095-7
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author Wang, Ya
Harding, Ian H.
Testa, Renee
Tonge, Bruce
Jones, Harvey
Seal, Marc
Ross, Nola
Chan, Raymond C. K.
van Beurden, Florian
Abu-Akel, Ahmad
Skafidas, Efstratios
Pantelis, Christos
author_facet Wang, Ya
Harding, Ian H.
Testa, Renee
Tonge, Bruce
Jones, Harvey
Seal, Marc
Ross, Nola
Chan, Raymond C. K.
van Beurden, Florian
Abu-Akel, Ahmad
Skafidas, Efstratios
Pantelis, Christos
author_sort Wang, Ya
collection PubMed
description Schizotypal disorder lies in the schizophrenia spectrum and is widely studied in adult populations. Schizotypal disorder in children (SDc) is less well described. This study examined brain morphological and functional connectivity abnormalities in SDc (12 SDc and 9 typically developing children), focusing on the default mode and executive control brain networks. Results indicated that SDc is associated with reduced grey matter volume (GMV) in superior and medial frontal gyri, and increased resting-state functional connectivity between the superior frontal gyrus and inferior parietal lobule, compared to typically developing children (cluster-level FWE-corrected p < 0.05). The brain structure abnormality (GMV in left superior frontal gyrus) was correlated with clinical symptoms in SDc (r = −0.66, p = 0.026) and functional connectivity abnormality was correlated with extra-dimensional shifting impairments in all participants (r = 0.62, p = 0.011), suggesting their contribution to the underlying mechanisms of clinical presentation. These preliminary results motivate further work to characterize the neural basis of SDc and its significance as a risk factor for later psychosis.
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spelling pubmed-70807712020-03-19 Structural and functional brain abnormalities in children with schizotypal disorder: a pilot study Wang, Ya Harding, Ian H. Testa, Renee Tonge, Bruce Jones, Harvey Seal, Marc Ross, Nola Chan, Raymond C. K. van Beurden, Florian Abu-Akel, Ahmad Skafidas, Efstratios Pantelis, Christos NPJ Schizophr Brief Communication Schizotypal disorder lies in the schizophrenia spectrum and is widely studied in adult populations. Schizotypal disorder in children (SDc) is less well described. This study examined brain morphological and functional connectivity abnormalities in SDc (12 SDc and 9 typically developing children), focusing on the default mode and executive control brain networks. Results indicated that SDc is associated with reduced grey matter volume (GMV) in superior and medial frontal gyri, and increased resting-state functional connectivity between the superior frontal gyrus and inferior parietal lobule, compared to typically developing children (cluster-level FWE-corrected p < 0.05). The brain structure abnormality (GMV in left superior frontal gyrus) was correlated with clinical symptoms in SDc (r = −0.66, p = 0.026) and functional connectivity abnormality was correlated with extra-dimensional shifting impairments in all participants (r = 0.62, p = 0.011), suggesting their contribution to the underlying mechanisms of clinical presentation. These preliminary results motivate further work to characterize the neural basis of SDc and its significance as a risk factor for later psychosis. Nature Publishing Group UK 2020-03-18 /pmc/articles/PMC7080771/ /pubmed/32188859 http://dx.doi.org/10.1038/s41537-020-0095-7 Text en © Crown 2020 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 Brief Communication
Wang, Ya
Harding, Ian H.
Testa, Renee
Tonge, Bruce
Jones, Harvey
Seal, Marc
Ross, Nola
Chan, Raymond C. K.
van Beurden, Florian
Abu-Akel, Ahmad
Skafidas, Efstratios
Pantelis, Christos
Structural and functional brain abnormalities in children with schizotypal disorder: a pilot study
title Structural and functional brain abnormalities in children with schizotypal disorder: a pilot study
title_full Structural and functional brain abnormalities in children with schizotypal disorder: a pilot study
title_fullStr Structural and functional brain abnormalities in children with schizotypal disorder: a pilot study
title_full_unstemmed Structural and functional brain abnormalities in children with schizotypal disorder: a pilot study
title_short Structural and functional brain abnormalities in children with schizotypal disorder: a pilot study
title_sort structural and functional brain abnormalities in children with schizotypal disorder: a pilot study
topic Brief Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7080771/
https://www.ncbi.nlm.nih.gov/pubmed/32188859
http://dx.doi.org/10.1038/s41537-020-0095-7
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