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...
Autores principales: | , , , , , , , , , , |
---|---|
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 |