Evidence map›Paper›PMID 39262181›Full record

Trial reportBrain and behavior2024

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

Joanne Ryan, Aung Zaw Zaw Phyo, Sebahate Pacolli Krasniqi, Selvi Izeti Carkaxhiu, Peter Fransquet, Sara Helene Kaas-Petersen, Dafina Arifaj Limani, Vjosa Devaja Xhemaili, Mimoza Salihu, Qendresa Prapashtica and 5 more

Abstract readRandomized Controlled Trial
In one paragraph

Trial report in Brain and behavior, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed, 1 pooled it
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Trial
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

15 authors.

Joanne RyanBiological Neuropsychiatry and Dementia Unit, School of Public Health and Preventative Medicine, Monash University, Melbourne, Australia.ORCID https://orcid.org/0000-0002-7039-6325
Aung Zaw Zaw PhyoBiological Neuropsychiatry and Dementia Unit, School of Public Health and Preventative Medicine, Monash University, Melbourne, Australia.
Sebahate Pacolli KrasniqiKosovo Rehabilitation Center for Torture Victims (KRCT), Pristina Kosovo, Australia.
Selvi Izeti CarkaxhiuKosovo Rehabilitation Center for Torture Victims (KRCT), Pristina Kosovo, Australia.
Peter FransquetFaculty of Health, School of Psychology, Centre for Social & Early Emotional Development, Deakin University, Geelong, Victoria, Australia.
Sara Helene Kaas-PetersenThe Danish Institute Against Torture (DIGNITY), Copenhagen, Denmark.
Dafina Arifaj LimaniKosovo Rehabilitation Center for Torture Victims (KRCT), Pristina Kosovo, Australia.
Vjosa Devaja XhemailiKosovo Rehabilitation Center for Torture Victims (KRCT), Pristina Kosovo, Australia.
Mimoza SalihuKosovo Rehabilitation Center for Torture Victims (KRCT), Pristina Kosovo, Australia.
Qendresa PrapashticaKosovo Rehabilitation Center for Torture Victims (KRCT), Pristina Kosovo, Australia.
Nebahate ZekajKosovo Rehabilitation Center for Torture Victims (KRCT), Pristina Kosovo, Australia.
Vesa TurjakaKosovo Rehabilitation Center for Torture Victims (KRCT), Pristina Kosovo, Australia.
Shr-Jie Wang *The Danish Institute Against Torture (DIGNITY), Copenhagen, Denmark.
Feride Rushiti *Kosovo Rehabilitation Center for Torture Victims (KRCT), Pristina Kosovo, Australia.
Line Hjort *Novo Nordisk Foundation Center for Basic Metabolic Research, Metabolic Epigenetics Group, Faculty of Health and Medical Sciences, University of Copenhagen, Copenhagen, Denmark.

Funding

British EmbassyDanish Diabetes and Endocrine AcademyDanish Institute Against TortureNational Health and Medical Research Council 2016438Novo Nordisk Fonden NNF17SA0031406Novo Nordisk Fonden NNF20SA0064340
6 · The paper itself

Abstract

introductionMaternal 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.

methodsA 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.

resultsSixty-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.

conclusionWe 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.

Indexed as

DNA MethylationFamily TherapyHydrocortisoneAdultChildEpigenesis, GeneticEpigenomeFemaleHumansKosovoMaleMothersPregnancyPrenatal Exposure Delayed EffectsSex OffensesHydrocortisoneDNA methylationintergenerationalinterventiontrauma

Identifiers

PMID39262181
PMCPMC11391026

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.