Structural brain morphometry as classifier and predictor of ADHD and reward-related comorbidities
Attention deficit/hyperactivity disorder (ADHD) is one of the most common neurodevelopmental disorders, and around two-thirds of affected children report persisting problems in adulthood. This negative trajectory is associated with high comorbidity with disorders like obesity, depression, or substan...
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Published in | Frontiers in psychiatry Vol. 13; p. 869627 |
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Main Authors | , , , , , |
Format | Journal Article |
Language | English |
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Frontiers Media S.A
12.09.2022
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ISSN | 1664-0640 1664-0640 |
DOI | 10.3389/fpsyt.2022.869627 |
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Abstract | Attention deficit/hyperactivity disorder (ADHD) is one of the most common neurodevelopmental disorders, and around two-thirds of affected children report persisting problems in adulthood. This negative trajectory is associated with high comorbidity with disorders like obesity, depression, or substance use disorder (SUD). Decreases in cortical volume and thickness have also been reported in depression, SUD, and obesity, but it is unclear whether structural brain alterations represent unique disorder-specific profiles. A transdiagnostic exploration of ADHD and typical comorbid disorders could help to understand whether specific morphometric brain changes are due to ADHD or, alternatively, to the comorbid disorders. In the current study, we studied the brain morphometry of 136 subjects with ADHD with and without comorbid depression, SUD, and obesity to test whether there are unique or common brain alterations. We employed a machine-learning-algorithm trained to classify subjects with ADHD in the large ENIGMA-ADHD dataset and used it to predict the diagnostic status of subjects with ADHD and/or comorbidities. The parcellation analysis demonstrated decreased cortical thickness in medial prefrontal areas that was associated with presence of any comorbidity. However, these results did not survive correction for multiple comparisons. Similarly, the machine learning analysis indicated that the predictive algorithm grouped most of our ADHD participants as belonging to the ADHD-group, but no systematic differences between comorbidity status came up. In sum, neither a classical comparison of segmented structural brain metrics nor an ML model based on the ADHD ENIGMA data differentiate between ADHD with and without comorbidities. As the ML model is based in part on adolescent brains, this might indicate that comorbid disorders and their brain changes are not captured by the ML model because it represents a different developmental brain trajectory. |
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AbstractList | Attention deficit/hyperactivity disorder (ADHD) is one of the most common neurodevelopmental disorders, and around two-thirds of affected children report persisting problems in adulthood. This negative trajectory is associated with high comorbidity with disorders like obesity, depression, or substance use disorder (SUD). Decreases in cortical volume and thickness have also been reported in depression, SUD, and obesity, but it is unclear whether structural brain alterations represent unique disorder-specific profiles. A transdiagnostic exploration of ADHD and typical comorbid disorders could help to understand whether specific morphometric brain changes are due to ADHD or, alternatively, to the comorbid disorders. In the current study, we studied the brain morphometry of 136 subjects with ADHD with and without comorbid depression, SUD, and obesity to test whether there are unique or common brain alterations. We employed a machine-learning-algorithm trained to classify subjects with ADHD in the large ENIGMA-ADHD dataset and used it to predict the diagnostic status of subjects with ADHD and/or comorbidities. The parcellation analysis demonstrated decreased cortical thickness in medial prefrontal areas that was associated with presence of any comorbidity. However, these results did not survive correction for multiple comparisons. Similarly, the machine learning analysis indicated that the predictive algorithm grouped most of our ADHD participants as belonging to the ADHD-group, but no systematic differences between comorbidity status came up. In sum, neither a classical comparison of segmented structural brain metrics nor an ML model based on the ADHD ENIGMA data differentiate between ADHD with and without comorbidities. As the ML model is based in part on adolescent brains, this might indicate that comorbid disorders and their brain changes are not captured by the ML model because it represents a different developmental brain trajectory.Attention deficit/hyperactivity disorder (ADHD) is one of the most common neurodevelopmental disorders, and around two-thirds of affected children report persisting problems in adulthood. This negative trajectory is associated with high comorbidity with disorders like obesity, depression, or substance use disorder (SUD). Decreases in cortical volume and thickness have also been reported in depression, SUD, and obesity, but it is unclear whether structural brain alterations represent unique disorder-specific profiles. A transdiagnostic exploration of ADHD and typical comorbid disorders could help to understand whether specific morphometric brain changes are due to ADHD or, alternatively, to the comorbid disorders. In the current study, we studied the brain morphometry of 136 subjects with ADHD with and without comorbid depression, SUD, and obesity to test whether there are unique or common brain alterations. We employed a machine-learning-algorithm trained to classify subjects with ADHD in the large ENIGMA-ADHD dataset and used it to predict the diagnostic status of subjects with ADHD and/or comorbidities. The parcellation analysis demonstrated decreased cortical thickness in medial prefrontal areas that was associated with presence of any comorbidity. However, these results did not survive correction for multiple comparisons. Similarly, the machine learning analysis indicated that the predictive algorithm grouped most of our ADHD participants as belonging to the ADHD-group, but no systematic differences between comorbidity status came up. In sum, neither a classical comparison of segmented structural brain metrics nor an ML model based on the ADHD ENIGMA data differentiate between ADHD with and without comorbidities. As the ML model is based in part on adolescent brains, this might indicate that comorbid disorders and their brain changes are not captured by the ML model because it represents a different developmental brain trajectory. Attention deficit/hyperactivity disorder (ADHD) is one of the most common neurodevelopmental disorders, and around two-thirds of affected children report persisting problems in adulthood. This negative trajectory is associated with high comorbidity with disorders like obesity, depression, or substance use disorder (SUD). Decreases in cortical volume and thickness have also been reported in depression, SUD, and obesity, but it is unclear whether structural brain alterations represent unique disorder-specific profiles. A transdiagnostic exploration of ADHD and typical comorbid disorders could help to understand whether specific morphometric brain changes are due to ADHD or, alternatively, to the comorbid disorders. In the current study, we studied the brain morphometry of 136 subjects with ADHD with and without comorbid depression, SUD, and obesity to test whether there are unique or common brain alterations. We employed a machine-learning-algorithm trained to classify subjects with ADHD in the large ENIGMA-ADHD dataset and used it to predict the diagnostic status of subjects with ADHD and/or comorbidities. The parcellation analysis demonstrated decreased cortical thickness in medial prefrontal areas that was associated with presence of any comorbidity. However, these results did not survive correction for multiple comparisons. Similarly, the machine learning analysis indicated that the predictive algorithm grouped most of our ADHD participants as belonging to the ADHD-group, but no systematic differences between comorbidity status came up. In sum, neither a classical comparison of segmented structural brain metrics nor an ML model based on the ADHD ENIGMA data differentiate between ADHD with and without comorbidities. As the ML model is based in part on adolescent brains, this might indicate that comorbid disorders and their brain changes are not captured by the ML model because it represents a different developmental brain trajectory. |
Author | Faraone, Stephen V. Reif, Andreas Grimm, Oliver Buitelaar, Jan Zhang-James, Yanli van Rooij, Daan |
AuthorAffiliation | 2 Department of Psychiatry and Behavioral Sciences, SUNY Upstate Medical University , Syracuse, NY , United States 3 Department of Psychiatry, Psychosomatic Medicine and Psychotherapy, University Hospital, Goethe University , Frankfurt , Germany 1 Department of Cognitive Neuroscience, Donders Institute for Brain, Cognition and Behavior, Radboud University Medical Center , Nijmegen , Netherlands |
AuthorAffiliation_xml | – name: 1 Department of Cognitive Neuroscience, Donders Institute for Brain, Cognition and Behavior, Radboud University Medical Center , Nijmegen , Netherlands – name: 2 Department of Psychiatry and Behavioral Sciences, SUNY Upstate Medical University , Syracuse, NY , United States – name: 3 Department of Psychiatry, Psychosomatic Medicine and Psychotherapy, University Hospital, Goethe University , Frankfurt , Germany |
Author_xml | – sequence: 1 givenname: Daan surname: van Rooij fullname: van Rooij, Daan – sequence: 2 givenname: Yanli surname: Zhang-James fullname: Zhang-James, Yanli – sequence: 3 givenname: Jan surname: Buitelaar fullname: Buitelaar, Jan – sequence: 4 givenname: Stephen V. surname: Faraone fullname: Faraone, Stephen V. – sequence: 5 givenname: Andreas surname: Reif fullname: Reif, Andreas – sequence: 6 givenname: Oliver surname: Grimm fullname: Grimm, Oliver |
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Cites_doi | 10.1176/ajp.2007.164.6.942 10.1038/s41386-019-0563-9 10.1371/journal.pone.0226518 10.1038/s41398-021-01201-4 10.1192/bjp.bp.112.123299 10.1016/j.neubiorev.2018.08.010 10.1038/s41380-020-01002-z 10.1177/1087054716646451 10.1093/schbul/sbab125 10.2217/npy.12.39 10.1016/j.euroneuro.2018.08.001 10.4088/JCP.12r08287 10.1176/ajp.150.6.885 10.1016/S1056-4993(18)30105-6 10.1016/S2215-0366(17)30049-4 10.1176/appi.ajp.2011.11030489 10.1176/appi.ajp.2018.17121383 10.1176/appi.ajp.2019.18091033 10.1017/S003329171100153X 10.1016/j.pscychresns.2013.06.004 10.1038/s41366-018-0164-4 10.3109/00952990.2015.1058389 10.1038/s41380-020-0774-9 10.1017/S003329170500471X 10.1016/j.neubiorev.2021.06.025 10.1016/j.jns.2020.117099 10.1177/1087054715626511 10.1016/j.euroneuro.2013.11.011 |
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Copyright | Copyright © 2022 van Rooij, Zhang-James, Buitelaar, Faraone, Reif and Grimm. Copyright © 2022 van Rooij, Zhang-James, Buitelaar, Faraone, Reif and Grimm. 2022 van Rooij, Zhang-James, Buitelaar, Faraone, Reif and Grimm |
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Notes | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 This article was submitted to Aging Psychiatry, a section of the journal Frontiers in Psychiatry Edited by: Francesco Oliva, University of Turin, Italy Reviewed by: Stefano Damiani, University of Pavia, Italy; Martin A. Katzman, START Clinic for Mood and Anxiety Disorders, Canada; Xiang-Zhen Kong, Graduate School, Zhejiang University, China |
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Title | Structural brain morphometry as classifier and predictor of ADHD and reward-related comorbidities |
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