White matter microstructure of the extended limbic system in male and female youth with conduct disorder.


Journal

Psychological medicine
ISSN: 1469-8978
Titre abrégé: Psychol Med
Pays: England
ID NLM: 1254142

Informations de publication

Date de publication:
01 2020
Historique:
pubmed: 31 1 2019
medline: 1 12 2020
entrez: 31 1 2019
Statut: ppublish

Résumé

Previous studies of conduct disorder (CD) have reported structural and functional alterations in the limbic system. However, the white matter tracts that connect limbic regions have not been comprehensively studied. The uncinate fasciculus (UF), a tract connecting limbic to prefrontal regions, has been implicated in CD. However, CD-related alterations in other limbic tracts, such as the cingulum and the fornix, have not been investigated. Furthermore, few studies have examined the influence of sex and none have been adequately powered to test whether the relationship between CD and structural connectivity differs by sex. We examined whether adolescent males and females with CD exhibit differences in structural connectivity compared with typically developing controls. We acquired diffusion-weighted magnetic resonance imaging data from 101 adolescents with CD (52 females) and 99 controls (50 females). Data were processed for deterministic spherical deconvolution tractography. Virtual dissections of the UF, the three subdivisions of the cingulum [retrosplenial cingulum (RSC), parahippocampal and subgenual cingulum], and the fornix were performed and measures of fractional anisotropy (FA) and hindrance-modulated orientational anisotropy (HMOA) were analysed. The CD group had lower FA and HMOA in the right RSC tract relative to controls. Importantly, these effects were moderated by sex - males with CD significantly lower FA compared to male controls, whereas CD and control females did not differ. Our results highlight the importance of considering sex when studying the neurobiological basis of CD. Sex differences in RSC connectivity may contribute to sex differences in the clinical presentation of CD.

Sections du résumé

BACKGROUND
Previous studies of conduct disorder (CD) have reported structural and functional alterations in the limbic system. However, the white matter tracts that connect limbic regions have not been comprehensively studied. The uncinate fasciculus (UF), a tract connecting limbic to prefrontal regions, has been implicated in CD. However, CD-related alterations in other limbic tracts, such as the cingulum and the fornix, have not been investigated. Furthermore, few studies have examined the influence of sex and none have been adequately powered to test whether the relationship between CD and structural connectivity differs by sex. We examined whether adolescent males and females with CD exhibit differences in structural connectivity compared with typically developing controls.
METHODS
We acquired diffusion-weighted magnetic resonance imaging data from 101 adolescents with CD (52 females) and 99 controls (50 females). Data were processed for deterministic spherical deconvolution tractography. Virtual dissections of the UF, the three subdivisions of the cingulum [retrosplenial cingulum (RSC), parahippocampal and subgenual cingulum], and the fornix were performed and measures of fractional anisotropy (FA) and hindrance-modulated orientational anisotropy (HMOA) were analysed.
RESULTS
The CD group had lower FA and HMOA in the right RSC tract relative to controls. Importantly, these effects were moderated by sex - males with CD significantly lower FA compared to male controls, whereas CD and control females did not differ.
CONCLUSIONS
Our results highlight the importance of considering sex when studying the neurobiological basis of CD. Sex differences in RSC connectivity may contribute to sex differences in the clinical presentation of CD.

Identifiants

pubmed: 30696514
pii: S0033291718003951
doi: 10.1017/S0033291718003951
doi:

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

58-67

Auteurs

Karen González-Madruga (K)

Department of Psychology, University of Southampton, Southampton, UK.

Jack Rogers (J)

School of Psychology and Birmingham University Imaging Centre, University of Birmingham, Birmingham, UK.

Nicola Toschi (N)

Department of Biomedicine and Prevention, University of Rome 'Tor Vergata', Rome, Italy.

Roberta Riccelli (R)

Department of Psychology, University of Southampton, Southampton, UK.

Areti Smaragdi (A)

Centre for Addiction and Mental Health, Toronto, Canada.

Ignazio Puzzo (I)

West London Mental Health Trust, Broadmoor High Secure Hospital, London, UK.

Roberta Clanton (R)

School of Psychology and Birmingham University Imaging Centre, University of Birmingham, Birmingham, UK.

Jesper Andersson (J)

FMRIB, John Radcliffe Hospital, University of Oxford, Oxford, UK.

Sarah Baumann (S)

Department of Child and Adolescent Psychiatry, Child Neuropsychology Section, Psychosomatics and Psychotherapy, University Hospital RWTH Aachen, Aachen, Germany.

Gregor Kohls (G)

Department of Child and Adolescent Psychiatry, Child Neuropsychology Section, Psychosomatics and Psychotherapy, University Hospital RWTH Aachen, Aachen, Germany.

Nora Raschle (N)

Department of Child and Adolescent Psychiatry, Psychiatric University Clinics and University of Basel, Basel, Switzerland.

Lynn Fehlbaum (L)

Department of Child and Adolescent Psychiatry, Psychiatric University Clinics and University of Basel, Basel, Switzerland.

Willeke Menks (W)

Department of Child and Adolescent Psychiatry, Psychiatric University Clinics and University of Basel, Basel, Switzerland.

Christina Stadler (C)

Department of Child and Adolescent Psychiatry, Psychiatric University Clinics and University of Basel, Basel, Switzerland.

Kerstin Konrad (K)

Department of Child and Adolescent Psychiatry, Child Neuropsychology Section, Psychosomatics and Psychotherapy, University Hospital RWTH Aachen, Aachen, Germany.

Christine M Freitag (CM)

Department of Child and Adolescent Psychiatry, Psychosomatics and Psychotherapy, University Hospital Frankfurt, Goethe University, Frankfurt am Main, Germany.

Stephane A De Brito (SA)

School of Psychology and Birmingham University Imaging Centre, University of Birmingham, Birmingham, UK.

Edmund Sonuga-Barke (E)

Child and Adolescent Psychiatry Department, Institute of Psychiatry, Psychology and Neuroscience, Kings College London, London, UK.

Graeme Fairchild (G)

Department of Psychology, University of Bath, Bath, UK.

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Classifications MeSH