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Sex differences in psychiatric comorbidity and clinical presentation in youths with conduct disorder

  • Kerstin Konrad
  • , Gregor Kohls
  • , Sarah Baumann
  • , Anka Bernhard
  • , Anne Martinelli
  • , Katharina Ackermann
  • , Areti Smaragdi
  • , Karen Gonzalez‐madruga
  • , Amy Wells
  • , Jack C. Rogers
  • , Ruth Pauli
  • , Roberta Clanton
  • , Rosalind Baker
  • , Linda Kersten
  • , Martin Prätzlich
  • , Helena Oldenhof
  • , Lucres Jansen
  • , Anneke Kleeven
  • , Aitana Bigorra
  • , Amaia Hervas
  • Iñaki Kerexeta‐lizeaga, Eva Sesma‐pardo, Miguel Angel Gonzalez‐torres, Réka Siklósi, Roberta Dochnal, Zacharias Kalogerakis, Mara Pirlympou, Leonidas Papadakos, Harriet Cornwell, Wolfgang Scharke, Dimitris Dikeos, Aranzazu Fernández‐rivas, Arne Popma, Christina Stadler, Beate Herpertz‐dahlmann, Stephane A. De Brito, Graeme Fairchild, Christine M. Freitag
  • JARA - Jülich Aachen Research Alliance
  • University Hospital RWTH Aachen
  • University Hospital Frankfurt
  • Centre of Addiction and Mental Health Toronto ON Canada
  • King's College London
  • Cardiff University
  • University of Birmingham
  • University Psychiatric Clinics Basel
  • VU University Medical Center
  • Child and Adolescent Mental Health Service University Hospital Mutua Terrassa Barcelona Spain
  • Basurto University Hospital
  • University of Szeged
  • National and Kapodistrian University of Athens
  • RWTH Aachen University

Research output: Contribution to journalArticlepeer-review

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Abstract

Background:
Conduct disorder (CD) rarely occurs alone but is typically accompanied by comorbid psychiatric disorders, which complicates the clinical presentation and treatment of affected youths. The aim of this study was to investigate sex differences in comorbidity pattern in CD and to systematically explore the ‘gender paradox’ and ‘delayed-onset pathway’ hypotheses of female CD.

Methods:
As part of the FemNAT-CD multisite study, semistructured clinical interviews and rating scales were used to perform a comprehensive phenotypic characterization of 454 girls and 295 boys with CD (9–18 years), compared to 864 sex- and age-matched typically developing controls.

Results:
Girls with CD exhibited higher rates of current major depression, anxiety disorders, post-traumatic stress disorder and borderline personality disorder, whereas boys with CD had higher rates of current attention-deficit/hyperactivity disorder. In line with the ‘gender paradox’ hypothesis, relative to boys, girls with CD showed significantly more lifetime psychiatric comorbidities (incl. Alcohol Use Disorder), which were accompanied by more severe CD symptoms. Female and male youths with CD also differed significantly in their CD symptom profiles and distribution of age-of-onset subtypes of CD (i.e. fewer girls with childhood-onset CD). In line with the ‘delayed-onset pathway’ hypothesis, girls with adolescent-onset CD showed similar levels of dimensional psychopathology like boys with childhood-onset CD, while boys with adolescent-onset CD had the lowest levels of internalizing psychopathology.

Conclusions:
Within the largest study of CD in girls performed to date, we found compelling evidence for sex differences in comorbidity patterns and clinical presentation of CD. Our findings further support aspects of the ‘gender paradox’ and ‘delayed-onset pathway’ hypotheses by showing that girls with CD had higher rates of comorbid lifetime mental disorders and functional impairments, and they usually developed CD during adolescence. These novel data on sex-specific clinical profiles of CD will be critical in informing intervention and prevention programmes.
Original languageEnglish
Pages (from-to)218-228
Number of pages11
JournalJournal of Child Psychology and Psychiatry
Volume63
Issue number2
Early online date19 May 2021
DOIs
Publication statusPublished - 28 Feb 2022

Bibliographical note

Funding Information:
The authors thank all participants and their families for taking part in this study. This study was funded by the European Commission's Seventh Framework Programme (FP7/2007‐2013) under Grant Agreement no. 602407 (FemNAT‐CD coordinator: Christine Freitag, University Hospital Frankfurt).

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

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