Methylation of the glucocorticoid receptor gene, nuclear receptor subfamily 3, group C, member 1 (NR3C1), in maltreated and nonmaltreated children: Associations with behavioral undercontrol, emotional lability/negativity, and externalizing and internalizing symptoms

Dante Cicchetti, Elizabeth D. Handley

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58 Scopus citations

Abstract

The present study examined the effect of various dimensions of child maltreatment (i.e., developmental timing of maltreatment, number of maltreatment subtypes, and chronicity of maltreatment) on methylation of the glucocorticoid receptor gene, nuclear receptor subfamily 3, group C, member 1 (NR3C1), and investigated the associations between NR3C1 methylation and child outcomes. Participants included 534 children who attended a research summer camp program for school-aged maltreated (53.4%) and nonmaltreated (46.6%) children from low socioeconomic backgrounds. Results show that children with early onset maltreatment evidence significant hypermethylation compared to nonmaltreated children. Moreover, more maltreatment subtypes experienced and more chronic maltreatment are both related to greater NR3C1 hypermethylation. Findings also indicate that hypermethylation of NR3C1 is linked with a number of negative child outcomes including greater emotional lability-negativity, higher levels of ego undercontrol, more externalizing behavior, and greater depressive symptoms. Together, results highlight the role of methylation of NR3C1 in the effects of child maltreatment on the development of emotion dysregulation and psychopathology.

Original languageEnglish (US)
Pages (from-to)1795-1806
Number of pages12
JournalDevelopment and psychopathology
Volume29
Issue number5
DOIs
StatePublished - Dec 1 2017

Bibliographical note

Funding Information:
We are grateful for the research support provided by the Emerald Foundation, Inc., and the Jacobs Foundation to Dante Cicchetti, and the National Institute of Mental Health (R01-MH83979 to D.C.).

Publisher Copyright:
Copyright © Cambridge University Press 2017.

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