An epigenome-wide study of a needs-based family intervention for offspring of trauma-exposed mothers in Kosovo.


Journal

Brain and behavior
ISSN: 2162-3279
Titre abrégé: Brain Behav
Pays: United States
ID NLM: 101570837

Informations de publication

Date de publication:
Sep 2024
Historique:
revised: 17 08 2024
received: 06 05 2024
accepted: 19 08 2024
medline: 12 9 2024
pubmed: 12 9 2024
entrez: 12 9 2024
Statut: ppublish

Résumé

Maternal stress and trauma during pregnancy have been shown to influence cortisol levels and epigenetic patterns, including DNA methylation, in the offspring. This study aimed to determine whether a tailor-made family intervention could help reduce cortisol levels in children born to traumatized mothers, and to determine whether it effected offspring DNA methylation. The secondary aim was to determine whether the family intervention influenced DNA methylation aging, a marker of biological aging. A needs-based family intervention was designed to help address relational difficulties and family functioning, and included a focus on family strengths and problem-solving patterns. Women survivors of sexual violence during the Kosovar war in 1998-1999, and their families (children with or without partners) were randomly assigned to 10 sessions of a family therapy over a 3-5-month period, or to a waitlist control group. Both mothers and children completed assessments prior to and after the intervention phase. Children's blood samples collected at these two time points were used to measure cortisol and epigenome-wide DNA methylation patterns (Illumina EPIC array). Cortisol levels, and genome-wide DNA methylation changes pre-/postintervention were compared between children in the intervention and the waitlist groups. DNA methylation age and accelerated biological aging were calculated. Sixty-two women-child dyads completed the study, 30 were assigned first to the intervention group, and 32 to the waitlist control group. In adjusted linear regression, the family intervention was associated with a significant decline in cortisol levels compared to the waitlist control (β = -124.72, 95% confidence interval [CI]: -197.4 to -52.1, p = .001). Children in the intervention group, compared to the waitlist control group, showed >1% differential methylation degree at 5819 CpG (5'-C-phosphate-G-3') sites across the genome (p < .01), with the largest methylation difference being 21%. However, none of these differences reached genome-wide significant levels. There was no significant difference in DNA methylation aging between the two groups. We find evidence that a tailored family-based intervention reduced stress levels in the children (based on cortisol levels), and modified DNA methylation levels at a number of sites across the genome. This study provides some preliminary evidence to suggest the potential for tailored interventions to help break the intergenerational transmission of trauma, however, large studies powered to detect associations at genome-wide significant levels are needed.

Identifiants

pubmed: 39262181
doi: 10.1002/brb3.70029
doi:

Substances chimiques

Hydrocortisone WI4X0X7BPJ

Types de publication

Journal Article Randomized Controlled Trial

Langues

eng

Sous-ensembles de citation

IM

Pagination

e70029

Subventions

Organisme : Novo Nordisk Fonden
ID : NNF17SA0031406
Organisme : Novo Nordisk Fonden
ID : NNF20SA0064340
Organisme : National Health and Medical Research Council
ID : 2016438
Organisme : Danish Diabetes and Endocrine Academy
Organisme : British Embassy
Organisme : Danish Institute Against Torture

Informations de copyright

© 2024 The Author(s). Brain and Behavior published by Wiley Periodicals LLC.

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Auteurs

Joanne Ryan (J)

Biological Neuropsychiatry and Dementia Unit, School of Public Health and Preventative Medicine, Monash University, Melbourne, Australia.

Aung Zaw Zaw Phyo (AZZ)

Biological Neuropsychiatry and Dementia Unit, School of Public Health and Preventative Medicine, Monash University, Melbourne, Australia.

Sebahate Pacolli Krasniqi (SP)

Kosovo Rehabilitation Center for Torture Victims (KRCT), Pristina Kosovo, Australia.

Selvi Izeti Carkaxhiu (SI)

Kosovo Rehabilitation Center for Torture Victims (KRCT), Pristina Kosovo, Australia.

Peter Fransquet (P)

Faculty of Health, School of Psychology, Centre for Social & Early Emotional Development, Deakin University, Geelong, Victoria, Australia.

Sara Helene Kaas-Petersen (SH)

The Danish Institute Against Torture (DIGNITY), Copenhagen, Denmark.

Dafina Arifaj Limani (DA)

Kosovo Rehabilitation Center for Torture Victims (KRCT), Pristina Kosovo, Australia.

Vjosa Devaja Xhemaili (VD)

Kosovo Rehabilitation Center for Torture Victims (KRCT), Pristina Kosovo, Australia.

Mimoza Salihu (M)

Kosovo Rehabilitation Center for Torture Victims (KRCT), Pristina Kosovo, Australia.

Qendresa Prapashtica (Q)

Kosovo Rehabilitation Center for Torture Victims (KRCT), Pristina Kosovo, Australia.

Nebahate Zekaj (N)

Kosovo Rehabilitation Center for Torture Victims (KRCT), Pristina Kosovo, Australia.

Vesa Turjaka (V)

Kosovo Rehabilitation Center for Torture Victims (KRCT), Pristina Kosovo, Australia.

Shr-Jie Wang (SJ)

The Danish Institute Against Torture (DIGNITY), Copenhagen, Denmark.

Feride Rushiti (F)

Kosovo Rehabilitation Center for Torture Victims (KRCT), Pristina Kosovo, Australia.

Line Hjort (L)

Novo Nordisk Foundation Center for Basic Metabolic Research, Metabolic Epigenetics Group, Faculty of Health and Medical Sciences, University of Copenhagen, Copenhagen, Denmark.
Department of Obstetrics, Center for Pregnant Women with Diabetes, Copenhagen University Hospital, Copenhagen, Denmark.

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