Mapping Cortical and Subcortical Asymmetry in Obsessive-Compulsive Disorder: Findings From the ENIGMA Consortium

dc.contributor.authorLázaro García, Luisa
dc.contributor.authorMenchón Magriñá, José Manuel
dc.contributor.authorSoriano Mas, Carles
dc.contributor.authorENIGMA OCD Working Group
dc.date.accessioned2020-11-09T10:09:00Z
dc.date.issued2020-06-15
dc.date.updated2020-11-09T10:09:01Z
dc.description.abstractBackground: Lateralized dysfunction has been suggested in obsessive-compulsive disorder (OCD). However, it is currently unclear whether OCD is characterized by abnormal patterns of brain structural asymmetry. Here we carried out what is by far the largest study of brain structural asymmetry in OCD. Methods: We studied a collection of 16 pediatric datasets (501 patients with OCD and 439 healthy control subjects), as well as 30 adult datasets (1777 patients and 1654 control subjects) from the OCD Working Group within the ENIGMA (Enhancing Neuro Imaging Genetics through Meta Analysis) Consortium. Asymmetries of the volumes of subcortical structures, and of measures of regional cortical thickness and surface areas, were assessed based on T1-weighted magnetic resonance imaging scans, using harmonized image analysis and quality control protocols. We investigated possible alterations of brain asymmetry in patients with OCD. We also explored potential associations of asymmetry with specific aspects of the disorder and medication status. Results: In the pediatric datasets, the largest case-control differences were observed for volume asymmetry of the thalamus (more leftward; Cohen's d = 0.19) and the pallidum (less leftward; d = -0.21). Additional analyses suggested putative links between these asymmetry patterns and medication status, OCD severity, or anxiety and depression comorbidities. No significant case-control differences were found in the adult datasets. Conclusions: The results suggest subtle changes of the average asymmetry of subcortical structures in pediatric OCD, which are not detectable in adults with the disorder. These findings may reflect altered neurodevelopmental processes in OCD.
dc.format.extent13 p.
dc.format.mimetypeapplication/pdf
dc.identifier.idgrec695039
dc.identifier.issn0006-3223
dc.identifier.pmid31178097
dc.identifier.urihttps://hdl.handle.net/2445/171874
dc.language.isoeng
dc.publisherElsevier B. V.
dc.relation.isformatofVersió postprint del document publicat a: https://doi.org/10.1016/j.biopsych.2019.04.022
dc.relation.ispartofBiological Psychiatry, 2020, vol. 87, num. 12, p. 1022-1034
dc.relation.projectIDinfo:eu-repo/grantAgreement/EC/FP7/278948/EU//TACTICS
dc.relation.urihttps://doi.org/10.1016/j.biopsych.2019.04.022
dc.rightscc-by-nc-nd (c) Elsevier B.V., 2020
dc.rights.accessRightsinfo:eu-repo/semantics/openAccess
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/3.0/es
dc.sourceArticles publicats en revistes (Ciències Clíniques)
dc.subject.classificationNeurosi obsessiva
dc.subject.classificationEscorça cerebral
dc.subject.otherObsessive-compulsive disorder
dc.subject.otherCerebral cortex
dc.titleMapping Cortical and Subcortical Asymmetry in Obsessive-Compulsive Disorder: Findings From the ENIGMA Consortium
dc.typeinfo:eu-repo/semantics/article
dc.typeinfo:eu-repo/semantics/acceptedVersion

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