Evidence map›Paper›PMID 29921868›Full record

ArticleTranslational psychiatry2018

NR3C1 hypermethylation in depressed and bullied adolescents.

Paschalis Efstathopoulos, Filip Andersson, Philippe A Melas, Liu L Yang, J Carlos Villaescusa, Joëlle Rȕegg, Tomas J Ekström, Yvonne Forsell, Maria Rosaria Galanti, Catharina Lavebratt

Open access · goldAbstract read
In one paragraph

Article in Translational psychiatry, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers, 4 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed, 4 pooled it
8.2field-weighted citation impact, top 2% of its field
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

36 citing papers in PubMed, 4 syntheses or guidelines pooled it, 68 citations in OpenAlex.

  1. Pooled it
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  14. Biomarkers in Child and Adolescent Depression.Child psychiatry and human development · 2023
    Review
  15. Glucocorticoid Receptor Gene (Alpha psychiatry · 2022
    Article
  16. Familial Linkage and Association of theInternational journal of molecular sciences · 2022
    Article
  17. DNA methylation in blood cells is associated with cortisol levels in offspring of mothers who had prenatal post-traumatic stress disorder.Stress and health : journal of the International Society for the Investigation of Stress · 2022
    Article
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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

10 authors at 3 institutions in 1 country.

Paschalis EfstathopoulosDepartment of Molecular Medicine and Surgery, Karolinska Institutet, Stockholm, Sweden.
Filip AnderssonDepartment of Public Health Sciences, Karolinska Institutet, Solna, Sweden.
Philippe A MelasCenter for Molecular Medicine, Karolinska University Hospital, Stockholm, Sweden.ORCID http://orcid.org/0000-0002-7889-9250
Liu L YangDepartment of Molecular Medicine and Surgery, Karolinska Institutet, Stockholm, Sweden.
J Carlos VillaescusaDepartment of Molecular Medicine and Surgery, Karolinska Institutet, Stockholm, Sweden.ORCID http://orcid.org/0000-0001-9456-9828
Joëlle RȕeggCenter for Molecular Medicine, Karolinska University Hospital, Stockholm, Sweden.
Tomas J EkströmCenter for Molecular Medicine, Karolinska University Hospital, Stockholm, Sweden.
Yvonne ForsellDepartment of Public Health Sciences, Karolinska Institutet, Solna, Sweden.
Maria Rosaria GalantiDepartment of Public Health Sciences, Karolinska Institutet, Solna, Sweden.
Catharina LavebrattDepartment of Molecular Medicine and Surgery, Karolinska Institutet, Stockholm, Sweden. catharina.lavebratt@ki.se.ORCID http://orcid.org/0000-0003-4987-2718
Karolinska University Hospital · SEStockholm County Council · SEKarolinska Institutet · SE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The disruption of key epigenetic processes during critical periods of brain development can increase an individual's vulnerability to psychopathology later in life. For instance, DNA methylation in the glucocorticoid receptor gene (NR3C1) in adulthood is known to be associated with early-life adversities and has been suggested to mediate the development of stress-related disorders. However, the association between NR3C1 methylation and the emergence of internalizing symptoms in childhood and adolescence has not been studied extensively. In the present report, we used saliva DNA from a cohort of Swedish adolescents (13-14 years old; N = 1149) to measure NR3C1 methylation in the exon 1F region. Internalizing psychopathological symptoms were assessed using the Center for Epidemiologic Studies Depression Scale for Children (CES-DC). We found that NR3C1 hypermethylation was cross-sectionally associated with high score for internalizing symptoms in the whole group as well as among the female participants. In addition, an analysis of social environmental stressors revealed that reports of bullied or lacking friends were significantly associated with NR3C1 hypermethylation. This cross-sectional association of NR3C1 exon 1F hypermethylation with internalizing psychopathology in adolescents, as well as with bullying and lack of friends are novel results in this field. Longitudinal studies are needed to address whether NR3C1 methylation mediates the link between social stressors and psychopathology in adolescence.

Indexed as

DNA MethylationAdolescentBullyingCohort StudiesCpG IslandsCross-Sectional StudiesDepressive DisorderEpigenesis, GeneticFemaleHumansLogistic ModelsMalePsychiatric Status Rating ScalesReceptors, GlucocorticoidSalivaStress, PsychologicalNR3C1 protein, humanReceptors, Glucocorticoid

Identifiers

PMID29921868
PMCPMC6008402
OpenAlexW2809655366

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

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.