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Involvement of the habenula in the pathophysiology of autism spectrum disorder

The habenula is a small epithalamic structure with widespread connections to multiple cortical, subcortical and brainstem regions. It has been identified as the central structure modulating the reward value of social interactions, behavioral adaptation, sensory integration and circadian rhythm. Auti...

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Autores principales: Germann, Jürgen, Gouveia, Flavia Venetucci, Brentani, Helena, Bedford, Saashi A., Tullo, Stephanie, Chakravarty, M. Mallar, Devenyi, Gabriel A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8551275/
https://www.ncbi.nlm.nih.gov/pubmed/34707133
http://dx.doi.org/10.1038/s41598-021-00603-0
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author Germann, Jürgen
Gouveia, Flavia Venetucci
Brentani, Helena
Bedford, Saashi A.
Tullo, Stephanie
Chakravarty, M. Mallar
Devenyi, Gabriel A.
author_facet Germann, Jürgen
Gouveia, Flavia Venetucci
Brentani, Helena
Bedford, Saashi A.
Tullo, Stephanie
Chakravarty, M. Mallar
Devenyi, Gabriel A.
author_sort Germann, Jürgen
collection PubMed
description The habenula is a small epithalamic structure with widespread connections to multiple cortical, subcortical and brainstem regions. It has been identified as the central structure modulating the reward value of social interactions, behavioral adaptation, sensory integration and circadian rhythm. Autism spectrum disorder (ASD) is characterized by social communication deficits, restricted interests, repetitive behaviors, and is frequently associated with altered sensory perception and mood and sleep disorders. The habenula is implicated in all these behaviors and results of preclinical studies suggest a possible involvement of the habenula in the pathophysiology of this disorder. Using anatomical magnetic resonance imaging and automated segmentation we show that the habenula is significantly enlarged in ASD subjects compared to controls across the entire age range studied (6–30 years). No differences were observed between sexes. Furthermore, support-vector machine modeling classified ASD with 85% accuracy (model using habenula volume, age and sex) and 64% accuracy in cross validation. The Social Responsiveness Scale (SRS) significantly differed between groups, however, it was not related to individual habenula volume. The present study is the first to provide evidence in human subjects of an involvement of the habenula in the pathophysiology of ASD.
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spelling pubmed-85512752021-11-01 Involvement of the habenula in the pathophysiology of autism spectrum disorder Germann, Jürgen Gouveia, Flavia Venetucci Brentani, Helena Bedford, Saashi A. Tullo, Stephanie Chakravarty, M. Mallar Devenyi, Gabriel A. Sci Rep Article The habenula is a small epithalamic structure with widespread connections to multiple cortical, subcortical and brainstem regions. It has been identified as the central structure modulating the reward value of social interactions, behavioral adaptation, sensory integration and circadian rhythm. Autism spectrum disorder (ASD) is characterized by social communication deficits, restricted interests, repetitive behaviors, and is frequently associated with altered sensory perception and mood and sleep disorders. The habenula is implicated in all these behaviors and results of preclinical studies suggest a possible involvement of the habenula in the pathophysiology of this disorder. Using anatomical magnetic resonance imaging and automated segmentation we show that the habenula is significantly enlarged in ASD subjects compared to controls across the entire age range studied (6–30 years). No differences were observed between sexes. Furthermore, support-vector machine modeling classified ASD with 85% accuracy (model using habenula volume, age and sex) and 64% accuracy in cross validation. The Social Responsiveness Scale (SRS) significantly differed between groups, however, it was not related to individual habenula volume. The present study is the first to provide evidence in human subjects of an involvement of the habenula in the pathophysiology of ASD. Nature Publishing Group UK 2021-10-27 /pmc/articles/PMC8551275/ /pubmed/34707133 http://dx.doi.org/10.1038/s41598-021-00603-0 Text en © The Author(s) 2021 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
Germann, Jürgen
Gouveia, Flavia Venetucci
Brentani, Helena
Bedford, Saashi A.
Tullo, Stephanie
Chakravarty, M. Mallar
Devenyi, Gabriel A.
Involvement of the habenula in the pathophysiology of autism spectrum disorder
title Involvement of the habenula in the pathophysiology of autism spectrum disorder
title_full Involvement of the habenula in the pathophysiology of autism spectrum disorder
title_fullStr Involvement of the habenula in the pathophysiology of autism spectrum disorder
title_full_unstemmed Involvement of the habenula in the pathophysiology of autism spectrum disorder
title_short Involvement of the habenula in the pathophysiology of autism spectrum disorder
title_sort involvement of the habenula in the pathophysiology of autism spectrum disorder
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8551275/
https://www.ncbi.nlm.nih.gov/pubmed/34707133
http://dx.doi.org/10.1038/s41598-021-00603-0
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