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Cortical signatures in behaviorally clustered autistic traits subgroups: a population-based study
Extensive heterogeneity in autism spectrum disorder (ASD) has hindered the characterization of consistent biomarkers, which has led to widespread negative results. Isolating homogenized subtypes could provide insight into underlying biological mechanisms and an overall better understanding of ASD. A...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7320967/ https://www.ncbi.nlm.nih.gov/pubmed/32594096 http://dx.doi.org/10.1038/s41398-020-00894-3 |
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author | Mihailov, Angeline Philippe, Cathy Gloaguen, Arnaud Grigis, Antoine Laidi, Charles Piguet, Camille Houenou, Josselin Frouin, Vincent |
author_facet | Mihailov, Angeline Philippe, Cathy Gloaguen, Arnaud Grigis, Antoine Laidi, Charles Piguet, Camille Houenou, Josselin Frouin, Vincent |
author_sort | Mihailov, Angeline |
collection | PubMed |
description | Extensive heterogeneity in autism spectrum disorder (ASD) has hindered the characterization of consistent biomarkers, which has led to widespread negative results. Isolating homogenized subtypes could provide insight into underlying biological mechanisms and an overall better understanding of ASD. A total of 1093 participants from the population-based “Healthy Brain Network” cohort (Child Mind Institute in the New York City area, USA) were selected based on score availability in behaviors relevant to ASD, aged 6–18 and IQ >= 70. All participants underwent an unsupervised clustering analysis on behavioral dimensions to reveal subgroups with ASD traits, identified by the presence of social deficits. Analysis revealed three socially impaired ASD traits subgroups: (1) high in emotionally dysfunctional traits, (2) high in ADHD-like traits, and (3) high in anxiety and depressive symptoms. 527 subjects had good quality structural MRI T1 data. Site effects on cortical features were adjusted using the ComBat method. Neuroimaging analyses compared cortical thickness, gyrification, and surface area, and were controlled for age, gender, and IQ, and corrected for multiple comparisons. Structural neuroimaging analyses contrasting one combined heterogeneous ASD traits group against controls did not yield any significant differences. Unique cortical signatures, however, were observed within each of the three individual ASD traits subgroups versus controls. These observations provide evidence of ASD traits subtypes, and confirm the necessity of applying dimensional approaches to extract meaningful differences, thus reducing heterogeneity and paving the way to better understanding ASD traits. |
format | Online Article Text |
id | pubmed-7320967 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-73209672020-06-30 Cortical signatures in behaviorally clustered autistic traits subgroups: a population-based study Mihailov, Angeline Philippe, Cathy Gloaguen, Arnaud Grigis, Antoine Laidi, Charles Piguet, Camille Houenou, Josselin Frouin, Vincent Transl Psychiatry Article Extensive heterogeneity in autism spectrum disorder (ASD) has hindered the characterization of consistent biomarkers, which has led to widespread negative results. Isolating homogenized subtypes could provide insight into underlying biological mechanisms and an overall better understanding of ASD. A total of 1093 participants from the population-based “Healthy Brain Network” cohort (Child Mind Institute in the New York City area, USA) were selected based on score availability in behaviors relevant to ASD, aged 6–18 and IQ >= 70. All participants underwent an unsupervised clustering analysis on behavioral dimensions to reveal subgroups with ASD traits, identified by the presence of social deficits. Analysis revealed three socially impaired ASD traits subgroups: (1) high in emotionally dysfunctional traits, (2) high in ADHD-like traits, and (3) high in anxiety and depressive symptoms. 527 subjects had good quality structural MRI T1 data. Site effects on cortical features were adjusted using the ComBat method. Neuroimaging analyses compared cortical thickness, gyrification, and surface area, and were controlled for age, gender, and IQ, and corrected for multiple comparisons. Structural neuroimaging analyses contrasting one combined heterogeneous ASD traits group against controls did not yield any significant differences. Unique cortical signatures, however, were observed within each of the three individual ASD traits subgroups versus controls. These observations provide evidence of ASD traits subtypes, and confirm the necessity of applying dimensional approaches to extract meaningful differences, thus reducing heterogeneity and paving the way to better understanding ASD traits. Nature Publishing Group UK 2020-06-27 /pmc/articles/PMC7320967/ /pubmed/32594096 http://dx.doi.org/10.1038/s41398-020-00894-3 Text en © The Author(s) 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 | Article Mihailov, Angeline Philippe, Cathy Gloaguen, Arnaud Grigis, Antoine Laidi, Charles Piguet, Camille Houenou, Josselin Frouin, Vincent Cortical signatures in behaviorally clustered autistic traits subgroups: a population-based study |
title | Cortical signatures in behaviorally clustered autistic traits subgroups: a population-based study |
title_full | Cortical signatures in behaviorally clustered autistic traits subgroups: a population-based study |
title_fullStr | Cortical signatures in behaviorally clustered autistic traits subgroups: a population-based study |
title_full_unstemmed | Cortical signatures in behaviorally clustered autistic traits subgroups: a population-based study |
title_short | Cortical signatures in behaviorally clustered autistic traits subgroups: a population-based study |
title_sort | cortical signatures in behaviorally clustered autistic traits subgroups: a population-based study |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7320967/ https://www.ncbi.nlm.nih.gov/pubmed/32594096 http://dx.doi.org/10.1038/s41398-020-00894-3 |
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