Callous-unemotional traits, low cortisol reactivity and physical aggression in children: findings from the Wirral Child Health and Development Study.


Journal

Translational psychiatry
ISSN: 2158-3188
Titre abrégé: Transl Psychiatry
Pays: United States
ID NLM: 101562664

Informations de publication

Date de publication:
11 02 2019
Historique:
received: 11 09 2018
accepted: 02 01 2019
revised: 27 11 2018
entrez: 12 2 2019
pubmed: 12 2 2019
medline: 14 6 2019
Statut: epublish

Résumé

Callous-unemotional (CU) traits are thought to confer risk for aggression via reduced amygdala responsivity to distress cues in others. Low cortisol reactivity is thought to confer risk for aggression via reduced arousal and this effect may be confined to boys. We tested the hypothesis that the association between childhood CU traits and aggression would be greatest in the absence of the inhibitory effects of cortisol reactivity, and that this effect would be sex dependent. Participants were 283 members of a stratified subsample within an epidemiological longitudinal cohort (WCHADS). Cortisol reactivity to a social stressor was assessed at 5 years. CU traits were reported by mothers at 5 years, and physical aggression by mothers and teachers at age 7. Results showed that CU traits were associated with elevated aggression at 7 years controlling for earlier aggression. There was no main effect of cortisol reactivity on regression. The association between CU traits and aggression was moderated by cortisol reactivity (p = .011) with a strong association between CU traits and aggression in the presence of low reactivity, and a small and non-significant association in the presence of high reactivity. This association was further moderated by child sex (p = .041) with the joint effect of high CU traits and low cortisol reactivity seen only in boys (p = .016). We report first evidence that a combined deficit in inhibitory processes associated with CU traits and low cortisol reactivity increases risk for childhood aggression, in a sex-dependent manner.

Identifiants

pubmed: 30741941
doi: 10.1038/s41398-019-0406-9
pii: 10.1038/s41398-019-0406-9
pmc: PMC6370839
doi:

Substances chimiques

Hydrocortisone WI4X0X7BPJ

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

79

Subventions

Organisme : Department of Health
Pays : United Kingdom
Organisme : Medical Research Council
ID : G0400577
Pays : United Kingdom
Organisme : Medical Research Council
ID : MR/L022257/2
Pays : United Kingdom
Organisme : Medical Research Council
ID : G0900654
Pays : United Kingdom
Organisme : Medical Research Council
ID : MR/L022257/1
Pays : United Kingdom

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Auteurs

Nicola Wright (N)

Biostatistics Department at the Institute of Psychiatry, King's College London, London, UK. nwright@liv.ac.uk.

Jonathan Hill (J)

School of Psychology and Clinical Language Sciences, University of Reading, Reading, UK.

Andrew Pickles (A)

Biostatistics Department at the Institute of Psychiatry, King's College London, London, UK.

Helen Sharp (H)

Department of Psychological Science, Institute of Psychology, Health and Society, University of Liverpool, Liverpool, UK.

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