Brain Functional Connectivity Correlates of Subclinical Obsessive-Compulsive Symptoms in Healthy Children.

functional connectivity functional magnetic resonance imaging obsessive-compulsive disorder subclinical symptoms symptom heterogeneity

Journal

Journal of the American Academy of Child and Adolescent Psychiatry
ISSN: 1527-5418
Titre abrégé: J Am Acad Child Adolesc Psychiatry
Pays: United States
ID NLM: 8704565

Informations de publication

Date de publication:
06 2021
Historique:
received: 05 02 2020
revised: 16 07 2020
accepted: 27 08 2020
pubmed: 21 9 2020
medline: 9 7 2021
entrez: 20 9 2020
Statut: ppublish

Résumé

Commonly observed subclinical obsessive-compulsive symptoms in healthy children may predispose to obsessive-compulsive disorder (OCD). Therefore, investigating the underlying neurobiology may be relevant to identify alterations in specific brain circuits potentially accounting for clinical heterogeneity in OCD without the confounding effects of clinical samples. We analyzed the brain correlates of different obsessive-compulsive symptoms in a large group of healthy children using functional connectivity measures. We evaluated 227 healthy children (52% girls; mean [SD] age 9.71 [0.86] years; range, 8-12.1 years). Participants underwent clinical assessment with the Obsessive-Compulsive Inventory-Child Version and a resting-state functional magnetic resonance imaging examination. Total and symptom-specific severity were correlated with voxelwise global functional connectivity degree values. Significant clusters were then used as seeds of interest in seed-to-voxel analyses. Modulating effects of age and sex were also assessed. Global functional connectivity of the left ventral putamen and medial dorsal thalamus correlated negatively with total obsessive-compulsive symptom severity. Seed-to-voxel analyses revealed specific negative correlations from these clusters with limbic, sensorimotor, and insular regions in association with obsessing, ordering, and doubt-checking symptoms, respectively. Hoarding symptoms were associated with negative correlations between the left medial dorsal thalamus and a widespread pattern of regions, with such associations modulated by sex and age. Our findings concur with prevailing neurobiological models of OCD on the importance of cortico-striato-thalamo-cortical dysfunction to account for symptom severity. Notably, we showed that changes in cortico-striato-thalamo-cortical connectivity are present at subclinical stages, which may result in an increased vulnerability for OCD. Moreover, we mapped different symptom dimensions onto specific cortico-striato-thalamo-cortical circuit attributes.

Identifiants

pubmed: 32950652
pii: S0890-8567(20)31836-0
doi: 10.1016/j.jaac.2020.08.435
pii:
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

757-767

Commentaires et corrections

Type : CommentIn

Informations de copyright

Copyright © 2020 American Academy of Child and Adolescent Psychiatry. Published by Elsevier Inc. All rights reserved.

Auteurs

Maria Suñol (M)

Hospital Universitari de Bellvitge, Institut d'Investigació Biomèdica de Bellvitge-IDIBELL, L'Hospitalet de Llobregat, Barcelona, Spain; Instituto de Salud Carlos III-Centro de Investigación Biomédica en Red de Salud Mental (CIBERSAM), Barcelona, Spain; Facultat de Medicina i Ciències de la Salut, Universitat de Barcelona, Spain.

Cristina Saiz-Masvidal (C)

Hospital Universitari de Bellvitge, Institut d'Investigació Biomèdica de Bellvitge-IDIBELL, L'Hospitalet de Llobregat, Barcelona, Spain; Facultat de Medicina i Ciències de la Salut, Universitat de Barcelona, Spain.

Oren Contreras-Rodríguez (O)

Hospital Universitari de Bellvitge, Institut d'Investigació Biomèdica de Bellvitge-IDIBELL, L'Hospitalet de Llobregat, Barcelona, Spain; Instituto de Salud Carlos III-Centro de Investigación Biomédica en Red de Salud Mental (CIBERSAM), Barcelona, Spain.

Dídac Macià (D)

Facultat de Medicina i Ciències de la Salut, Universitat de Barcelona, Spain; Institut Guttmann of the Universitat Autònoma de Barcelona, Badalona, Spain.

Gerard Martínez-Vilavella (G)

MRI Research Unit, Hospital del Mar, Barcelona, Spain.

Ignacio Martínez-Zalacaín (I)

Hospital Universitari de Bellvitge, Institut d'Investigació Biomèdica de Bellvitge-IDIBELL, L'Hospitalet de Llobregat, Barcelona, Spain; Facultat de Medicina i Ciències de la Salut, Universitat de Barcelona, Spain.

José Manuel Menchón (JM)

Hospital Universitari de Bellvitge, Institut d'Investigació Biomèdica de Bellvitge-IDIBELL, L'Hospitalet de Llobregat, Barcelona, Spain; Instituto de Salud Carlos III-Centro de Investigación Biomédica en Red de Salud Mental (CIBERSAM), Barcelona, Spain; Facultat de Medicina i Ciències de la Salut, Universitat de Barcelona, Spain.

Jesús Pujol (J)

Instituto de Salud Carlos III-Centro de Investigación Biomédica en Red de Salud Mental (CIBERSAM), Barcelona, Spain; MRI Research Unit, Hospital del Mar, Barcelona, Spain.

Jordi Sunyer (J)

Institut de Salut Global de Barcelona (ISGLOBAL), Centre de Recerca en Epidemiologia Ambiental (CREAL), Barcelona, Spain; Universitat Pompeu Fabra, Barcelona, Spain; Instituto de Salud Carlos III-Centro de Investigación Biomédica en Red de Epidemiología y Salud Pública (CIBERESP), Barcelona, Spain; Institut Hospital del Mar d'Investigacions Mèdiques (IMIM), Barcelona, Spain.

Carles Soriano-Mas (C)

Hospital Universitari de Bellvitge, Institut d'Investigació Biomèdica de Bellvitge-IDIBELL, L'Hospitalet de Llobregat, Barcelona, Spain; Instituto de Salud Carlos III-Centro de Investigación Biomédica en Red de Salud Mental (CIBERSAM), Barcelona, Spain; Universitat Autònoma de Barcelona, Barcelona, Spain. Electronic address: csoriano@idibell.cat.

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Classifications MeSH