Evidence map›Paper›PMID 24475181›Full record

ArticlePloS one2014

DNA methylation signature of childhood chronic physical aggression in T cells of both men and women.

Claire Guillemin, Nadine Provençal, Matthew Suderman, Sylvana M Côté, Frank Vitaro, Michael Hallett, Richard E Tremblay, Moshe Szyf

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed, 3 pooled it
5.1field-weighted citation impact, top 4% 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

26 citing papers in PubMed, 3 syntheses or guidelines pooled it, 85 citations in OpenAlex.

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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

8 authors at 4 institutions in 3 countries.

Claire GuilleminDepartment of Pharmacology & Therapeutics, McGill University, Montreal, Quebec, Canada ; Research Unit on Children's Psycho-Social Maladjustment and Ste-Justine Hospital Research Center, University of Montreal, Montreal, Quebec, Canada ; Sackler Program for Epigenetics and Psychobiology, McGill University, Montreal, Quebec, Canada.
Nadine ProvençalDepartment of Pharmacology & Therapeutics, McGill University, Montreal, Quebec, Canada ; Research Unit on Children's Psycho-Social Maladjustment and Ste-Justine Hospital Research Center, University of Montreal, Montreal, Quebec, Canada ; Sackler Program for Epigenetics and Psychobiology, McGill University, Montreal, Quebec, Canada.
Matthew SudermanDepartment of Pharmacology & Therapeutics, McGill University, Montreal, Quebec, Canada ; Sackler Program for Epigenetics and Psychobiology, McGill University, Montreal, Quebec, Canada ; McGill Centre for Bioinformatics, McGill University, Montreal, Quebec, Canada.
Sylvana M CôtéResearch Unit on Children's Psycho-Social Maladjustment and Ste-Justine Hospital Research Center, University of Montreal, Montreal, Quebec, Canada ; INSERM U669, Paris, France ; School of Social and Preventive Medicine, University of Montreal, Montreal, Quebec, Canada.
Frank VitaroResearch Unit on Children's Psycho-Social Maladjustment and Ste-Justine Hospital Research Center, University of Montreal, Montreal, Quebec, Canada ; School of Psycho-Education, University of Montreal, Montreal, Quebec, Canada.
Michael HallettMcGill Centre for Bioinformatics, McGill University, Montreal, Quebec, Canada.
Richard E TremblayResearch Unit on Children's Psycho-Social Maladjustment and Ste-Justine Hospital Research Center, University of Montreal, Montreal, Quebec, Canada ; Department of Psychology and Pediatrics, University of Montreal, Montreal, Quebec, Canada ; School of Public Health and Population Sciences, University College Dublin, Dublin, Ireland ; INSERM U669, Paris, France.
Moshe SzyfDepartment of Pharmacology & Therapeutics, McGill University, Montreal, Quebec, Canada ; Sackler Program for Epigenetics and Psychobiology, McGill University, Montreal, Quebec, Canada.
McGill University · CAUniversité de Montréal · CAInserm · FRResearch Unit on Children's Psychosocial Maladjustment · CA

Funding

Canadian Institutes of Health Research MOP-42411
6 · The paper itself

Abstract

backgroundHigh frequency of physical aggression is the central feature of severe conduct disorder and is associated with a wide range of social, mental and physical health problems. We have previously tested the hypothesis that differential DNA methylation signatures in peripheral T cells are associated with a chronic aggression trajectory in males. Despite the fact that sex differences appear to play a pivotal role in determining the development, magnitude and frequency of aggression, most of previous studies focused on males, so little is known about female chronic physical aggression. We therefore tested here whether or not there is a signature of physical aggression in female DNA methylation and, if there is, how it relates to the signature observed in males. METHODOLOGY/PRINCIPAL

findingsMethylation profiles were created using the method of methylated DNA immunoprecipitation (MeDIP) followed by microarray hybridization and statistical and bioinformatic analyses on T cell DNA obtained from adult women who were found to be on a chronic physical aggression trajectory (CPA) between 6 and 12 years of age compared to women who followed a normal physical aggression trajectory. We confirmed the existence of a well-defined, genome-wide signature of DNA methylation associated with chronic physical aggression in the peripheral T cells of adult females that includes many of the genes similarly associated with physical aggression in the same cell types of adult males.

conclusionsThis study in a small number of women presents preliminary evidence for a genome-wide variation in promoter DNA methylation that associates with CPA in women that warrant larger studies for further verification. A significant proportion of these associations were previously observed in men with CPA supporting the hypothesis that the epigenetic signature of early life aggression in females is composed of a component specific to females and another common to both males and females.

Indexed as

Genome, HumanPromoter Regions, GeneticTranscriptomeAdultAggressionCarrier ProteinsChildDNA MethylationFemaleGene Expression ProfilingHumansMaleMolecular Sequence AnnotationNucleotide MotifsReceptors, GlucocorticoidT-LymphocytesCarrier Proteinscorticotropin releasing factor-binding proteinNR3C1 protein, humanReceptors, GlucocorticoidTPH2 protein, humanTryptophan Hydroxylase

Identifiers

PMID24475181
PMCPMC3901708
OpenAlexW2064919449

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.