Cargando…

Shared endo-phenotypes of default mode dysfunction in attention deficit/hyperactivity disorder and autism spectrum disorder

Categorical diagnoses from the Diagnostic and Statistical Manual of Mental Disorders (DSM) or International Classification of Diseases (ICD) manuals are increasingly found to be incongruent with emerging neuroscientific evidence that points towards shared neurobiological dysfunction underlying atten...

Descripción completa

Detalles Bibliográficos
Autores principales: Kernbach, Julius M., Satterthwaite, Theodore D., Bassett, Danielle S., Smallwood, Jonathan, Margulies, Daniel, Krall, Sarah, Shaw, Philip, Varoquaux, Gaël, Thirion, Bertrand, Konrad, Kerstin, Bzdok, Danilo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6050263/
https://www.ncbi.nlm.nih.gov/pubmed/30018328
http://dx.doi.org/10.1038/s41398-018-0179-6
_version_ 1783340296265793536
author Kernbach, Julius M.
Satterthwaite, Theodore D.
Bassett, Danielle S.
Smallwood, Jonathan
Margulies, Daniel
Krall, Sarah
Shaw, Philip
Varoquaux, Gaël
Thirion, Bertrand
Konrad, Kerstin
Bzdok, Danilo
author_facet Kernbach, Julius M.
Satterthwaite, Theodore D.
Bassett, Danielle S.
Smallwood, Jonathan
Margulies, Daniel
Krall, Sarah
Shaw, Philip
Varoquaux, Gaël
Thirion, Bertrand
Konrad, Kerstin
Bzdok, Danilo
author_sort Kernbach, Julius M.
collection PubMed
description Categorical diagnoses from the Diagnostic and Statistical Manual of Mental Disorders (DSM) or International Classification of Diseases (ICD) manuals are increasingly found to be incongruent with emerging neuroscientific evidence that points towards shared neurobiological dysfunction underlying attention deficit/hyperactivity disorder and autism spectrum disorder. Using resting-state functional magnetic resonance imaging data, functional connectivity of the default mode network, the dorsal attention and salience network was studied in 1305 typically developing and diagnosed participants. A transdiagnostic hierarchical Bayesian modeling framework combining Indian Buffet Processes and Latent Dirichlet Allocation was proposed to address the urgent need for objective brain-derived measures that can acknowledge shared brain network dysfunction in both disorders. We identified three main variation factors characterized by distinct coupling patterns of the temporoparietal cortices in the default mode network with the dorsal attention and salience network. The brain-derived factors were demonstrated to effectively capture the underlying neural dysfunction shared in both disorders more accurately, and to enable more reliable diagnoses of neurobiological dysfunction. The brain-derived phenotypes alone allowed for a classification accuracy reflecting an underlying neuropathology of 67.33% (+/−3.07) in new individuals, which significantly outperformed the 46.73% (+/−3.97) accuracy of categorical diagnoses. Our results provide initial evidence that shared neural dysfunction in ADHD and ASD can be derived from conventional brain recordings in a data-led fashion. Our work is encouraging to pursue a translational endeavor to find and further study brain-derived phenotypes, which could potentially be used to improve clinical decision-making and optimize treatment in the future.
format Online
Article
Text
id pubmed-6050263
institution National Center for Biotechnology Information
language English
publishDate 2018
publisher Nature Publishing Group UK
record_format MEDLINE/PubMed
spelling pubmed-60502632018-07-18 Shared endo-phenotypes of default mode dysfunction in attention deficit/hyperactivity disorder and autism spectrum disorder Kernbach, Julius M. Satterthwaite, Theodore D. Bassett, Danielle S. Smallwood, Jonathan Margulies, Daniel Krall, Sarah Shaw, Philip Varoquaux, Gaël Thirion, Bertrand Konrad, Kerstin Bzdok, Danilo Transl Psychiatry Article Categorical diagnoses from the Diagnostic and Statistical Manual of Mental Disorders (DSM) or International Classification of Diseases (ICD) manuals are increasingly found to be incongruent with emerging neuroscientific evidence that points towards shared neurobiological dysfunction underlying attention deficit/hyperactivity disorder and autism spectrum disorder. Using resting-state functional magnetic resonance imaging data, functional connectivity of the default mode network, the dorsal attention and salience network was studied in 1305 typically developing and diagnosed participants. A transdiagnostic hierarchical Bayesian modeling framework combining Indian Buffet Processes and Latent Dirichlet Allocation was proposed to address the urgent need for objective brain-derived measures that can acknowledge shared brain network dysfunction in both disorders. We identified three main variation factors characterized by distinct coupling patterns of the temporoparietal cortices in the default mode network with the dorsal attention and salience network. The brain-derived factors were demonstrated to effectively capture the underlying neural dysfunction shared in both disorders more accurately, and to enable more reliable diagnoses of neurobiological dysfunction. The brain-derived phenotypes alone allowed for a classification accuracy reflecting an underlying neuropathology of 67.33% (+/−3.07) in new individuals, which significantly outperformed the 46.73% (+/−3.97) accuracy of categorical diagnoses. Our results provide initial evidence that shared neural dysfunction in ADHD and ASD can be derived from conventional brain recordings in a data-led fashion. Our work is encouraging to pursue a translational endeavor to find and further study brain-derived phenotypes, which could potentially be used to improve clinical decision-making and optimize treatment in the future. Nature Publishing Group UK 2018-07-17 /pmc/articles/PMC6050263/ /pubmed/30018328 http://dx.doi.org/10.1038/s41398-018-0179-6 Text en © The Author(s) 2018 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
Kernbach, Julius M.
Satterthwaite, Theodore D.
Bassett, Danielle S.
Smallwood, Jonathan
Margulies, Daniel
Krall, Sarah
Shaw, Philip
Varoquaux, Gaël
Thirion, Bertrand
Konrad, Kerstin
Bzdok, Danilo
Shared endo-phenotypes of default mode dysfunction in attention deficit/hyperactivity disorder and autism spectrum disorder
title Shared endo-phenotypes of default mode dysfunction in attention deficit/hyperactivity disorder and autism spectrum disorder
title_full Shared endo-phenotypes of default mode dysfunction in attention deficit/hyperactivity disorder and autism spectrum disorder
title_fullStr Shared endo-phenotypes of default mode dysfunction in attention deficit/hyperactivity disorder and autism spectrum disorder
title_full_unstemmed Shared endo-phenotypes of default mode dysfunction in attention deficit/hyperactivity disorder and autism spectrum disorder
title_short Shared endo-phenotypes of default mode dysfunction in attention deficit/hyperactivity disorder and autism spectrum disorder
title_sort shared endo-phenotypes of default mode dysfunction in attention deficit/hyperactivity disorder and autism spectrum disorder
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6050263/
https://www.ncbi.nlm.nih.gov/pubmed/30018328
http://dx.doi.org/10.1038/s41398-018-0179-6
work_keys_str_mv AT kernbachjuliusm sharedendophenotypesofdefaultmodedysfunctioninattentiondeficithyperactivitydisorderandautismspectrumdisorder
AT satterthwaitetheodored sharedendophenotypesofdefaultmodedysfunctioninattentiondeficithyperactivitydisorderandautismspectrumdisorder
AT bassettdanielles sharedendophenotypesofdefaultmodedysfunctioninattentiondeficithyperactivitydisorderandautismspectrumdisorder
AT smallwoodjonathan sharedendophenotypesofdefaultmodedysfunctioninattentiondeficithyperactivitydisorderandautismspectrumdisorder
AT marguliesdaniel sharedendophenotypesofdefaultmodedysfunctioninattentiondeficithyperactivitydisorderandautismspectrumdisorder
AT krallsarah sharedendophenotypesofdefaultmodedysfunctioninattentiondeficithyperactivitydisorderandautismspectrumdisorder
AT shawphilip sharedendophenotypesofdefaultmodedysfunctioninattentiondeficithyperactivitydisorderandautismspectrumdisorder
AT varoquauxgael sharedendophenotypesofdefaultmodedysfunctioninattentiondeficithyperactivitydisorderandautismspectrumdisorder
AT thirionbertrand sharedendophenotypesofdefaultmodedysfunctioninattentiondeficithyperactivitydisorderandautismspectrumdisorder
AT konradkerstin sharedendophenotypesofdefaultmodedysfunctioninattentiondeficithyperactivitydisorderandautismspectrumdisorder
AT bzdokdanilo sharedendophenotypesofdefaultmodedysfunctioninattentiondeficithyperactivitydisorderandautismspectrumdisorder