The link between parental psychological control, depressive symptoms and epigenetic changes in the glucocorticoid receptor gene (NR3C1).


Journal

Physiology & behavior
ISSN: 1873-507X
Titre abrégé: Physiol Behav
Pays: United States
ID NLM: 0151504

Informations de publication

Date de publication:
01 12 2020
Historique:
received: 26 06 2020
revised: 20 08 2020
accepted: 09 09 2020
pubmed: 22 9 2020
medline: 22 6 2021
entrez: 21 9 2020
Statut: ppublish

Résumé

This paper examines the relationship between parental Psychological Control (PC) and depressive symptoms in adolescents and assesses whether this relationship was mediated by DNA methylation, focusing on the glucocorticoid receptor gene (NR3C1), which plays a crucial role in HPA-axis functioning and is linked to environmental stress and depression. This is among the very few studies that looked at the relation between DNA methylation, environmental stress and depression in family trios. The study cohort consisted of 250 families: father, mother and a biologically related adolescent (adolescents (48.9% boys), mean age: 15.14, SD= 1.9; mean age mothers: 45.83, SD= 4.2; mean age fathers: 47.77, SD= 4.7). Depressive symptoms and PC were measured in adolescents and in both parents. DNA methylation levels in NR3C1 were examined in all participants. Depressive symptoms in adolescents were predicted by PC of both mothers and fathers. Moreover, maternal depressive symptoms were associated with maternal PC, and fathers' depressive symptoms and PC. In fathers, only the level of their self-reported PC was associated with their depressive symptoms. There was no relation between adolescents' DNA methylation and depressive symptoms or the level of parental PC. Yet, there was a significant association between maternal depressive symptoms and maternal epigenetic patterns in NR3C1. These findings highlight the need for more research in order to better understand the biological and contextual mechanisms through which parenting and parental emotional well-being is related to the development of psychopathology.

Identifiants

pubmed: 32956684
pii: S0031-9384(20)30484-4
doi: 10.1016/j.physbeh.2020.113170
pii:
doi:

Substances chimiques

Glucocorticoids 0
NR3C1 protein, human 0
Receptors, Glucocorticoid 0

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

113170

Informations de copyright

Copyright © 2020. Published by Elsevier Inc.

Auteurs

V Chubar (V)

KU Leuven, Mind-Body Research Group, Department of Neuroscience, B-3000 Leuven, Belgium. Electronic address: viktoriia.chubar@kuleuven.be.

P Luyten (P)

KU Leuven, Faculty of Psychology and Educational Sciences, B-3000 Leuven, Belgium; University College London, Research Department of Clinical, Educational and Health Psychology, London, UK.

L Goossens (L)

KU Leuven, School Psychology and Child and Adolescent Development Research Unit, Faculty of Psychology and Educational Sciences, KU Leuven, B-3000 Leuven, Belgium.

B Bekaert (B)

KU Leuven, University Hospitals Leuven, Department of Forensic Medicine, Laboratory of Forensic Genetics and Molecular Archaeology, B-3000 Leuven, Belgium; KU Leuven, Department of Imaging and Pathology, B-3000 Leuven, Belgium.

D Bleys (D)

KU Leuven, Faculty of Psychology and Educational Sciences, B-3000 Leuven, Belgium.

B Soenens (B)

Ghent university, Department of Developmental, Personality and Social Psychology, Ghent, Belgium.

S Claes (S)

KU Leuven, Mind-Body Research Group, Department of Neuroscience, B-3000 Leuven, Belgium; KU Leuven, University Psychiatric Center KU Leuven, B-3000 Leuven, Belgium.

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Classifications MeSH