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Atypical functional connectome hierarchy in autism
One paradox of autism is the co-occurrence of deficits in sensory and higher-order socio-cognitive processing. Here, we examined whether these phenotypical patterns may relate to an overarching system-level imbalance—specifically a disruption in macroscale hierarchy affecting integration and segrega...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6399265/ https://www.ncbi.nlm.nih.gov/pubmed/30833582 http://dx.doi.org/10.1038/s41467-019-08944-1 |
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author | Hong, Seok-Jun Vos de Wael, Reinder Bethlehem, Richard A. I. Lariviere, Sara Paquola, Casey Valk, Sofie L. Milham, Michael P. Di Martino, Adriana Margulies, Daniel S. Smallwood, Jonathan Bernhardt, Boris C. |
author_facet | Hong, Seok-Jun Vos de Wael, Reinder Bethlehem, Richard A. I. Lariviere, Sara Paquola, Casey Valk, Sofie L. Milham, Michael P. Di Martino, Adriana Margulies, Daniel S. Smallwood, Jonathan Bernhardt, Boris C. |
author_sort | Hong, Seok-Jun |
collection | PubMed |
description | One paradox of autism is the co-occurrence of deficits in sensory and higher-order socio-cognitive processing. Here, we examined whether these phenotypical patterns may relate to an overarching system-level imbalance—specifically a disruption in macroscale hierarchy affecting integration and segregation of unimodal and transmodal networks. Combining connectome gradient and stepwise connectivity analysis based on task-free functional magnetic resonance imaging (fMRI), we demonstrated atypical connectivity transitions between sensory and higher-order default mode regions in a large cohort of individuals with autism relative to typically-developing controls. Further analyses indicated that reduced differentiation related to perturbed stepwise connectivity from sensory towards transmodal areas, as well as atypical long-range rich-club connectivity. Supervised pattern learning revealed that hierarchical features predicted deficits in social cognition and low-level behavioral symptoms, but not communication-related symptoms. Our findings provide new evidence for imbalances in network hierarchy in autism, which offers a parsimonious reference frame to consolidate its diverse features. |
format | Online Article Text |
id | pubmed-6399265 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-63992652019-03-06 Atypical functional connectome hierarchy in autism Hong, Seok-Jun Vos de Wael, Reinder Bethlehem, Richard A. I. Lariviere, Sara Paquola, Casey Valk, Sofie L. Milham, Michael P. Di Martino, Adriana Margulies, Daniel S. Smallwood, Jonathan Bernhardt, Boris C. Nat Commun Article One paradox of autism is the co-occurrence of deficits in sensory and higher-order socio-cognitive processing. Here, we examined whether these phenotypical patterns may relate to an overarching system-level imbalance—specifically a disruption in macroscale hierarchy affecting integration and segregation of unimodal and transmodal networks. Combining connectome gradient and stepwise connectivity analysis based on task-free functional magnetic resonance imaging (fMRI), we demonstrated atypical connectivity transitions between sensory and higher-order default mode regions in a large cohort of individuals with autism relative to typically-developing controls. Further analyses indicated that reduced differentiation related to perturbed stepwise connectivity from sensory towards transmodal areas, as well as atypical long-range rich-club connectivity. Supervised pattern learning revealed that hierarchical features predicted deficits in social cognition and low-level behavioral symptoms, but not communication-related symptoms. Our findings provide new evidence for imbalances in network hierarchy in autism, which offers a parsimonious reference frame to consolidate its diverse features. Nature Publishing Group UK 2019-03-04 /pmc/articles/PMC6399265/ /pubmed/30833582 http://dx.doi.org/10.1038/s41467-019-08944-1 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 Hong, Seok-Jun Vos de Wael, Reinder Bethlehem, Richard A. I. Lariviere, Sara Paquola, Casey Valk, Sofie L. Milham, Michael P. Di Martino, Adriana Margulies, Daniel S. Smallwood, Jonathan Bernhardt, Boris C. Atypical functional connectome hierarchy in autism |
title | Atypical functional connectome hierarchy in autism |
title_full | Atypical functional connectome hierarchy in autism |
title_fullStr | Atypical functional connectome hierarchy in autism |
title_full_unstemmed | Atypical functional connectome hierarchy in autism |
title_short | Atypical functional connectome hierarchy in autism |
title_sort | atypical functional connectome hierarchy in autism |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6399265/ https://www.ncbi.nlm.nih.gov/pubmed/30833582 http://dx.doi.org/10.1038/s41467-019-08944-1 |
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