Evidence map›Paper›PMID 27520745›Full record

ArticleAutism research : official journal of the International Society for Autism Research2017

Prenatal stress exposure, oxytocin receptor gene (OXTR) methylation, and child autistic traits: The moderating role of OXTR rs53576 genotype.

Jolien Rijlaarsdam, Marinus H van IJzendoorn, Frank C Verhulst, Vincent W V Jaddoe, Janine F Felix, Henning Tiemeier, Marian J Bakermans-Kranenburg

Open access · greenAbstract read
In one paragraph

Article in Autism research : official journal of the International Society for Autism Research, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 46 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
46citing papers in PubMed, 3 pooled it
14.5field-weighted citation impact, top 1% 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

46 citing papers in PubMed, 3 syntheses or guidelines pooled it, 93 citations in OpenAlex.

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  12. A journey from speech to dance through the field of oxytocin.Comprehensive psychoneuroendocrinology · 2023
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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

7 authors at 3 institutions in 1 country.

Jolien RijlaarsdamCentre for Child and Family Studies, Leiden University, Leiden, The Netherlands.
Marinus H van IJzendoornCentre for Child and Family Studies, Leiden University, Leiden, The Netherlands.
Frank C VerhulstDepartment of Child and Adolescent Psychiatry/Psychology, Erasmus MC-University Medical Center Rotterdam, Rotterdam, The Netherlands.
Vincent W V JaddoeGeneration R Study Group, Erasmus MC-University Medical Center Rotterdam, Rotterdam, The Netherlands.
Janine F FelixDepartment of Epidemiology, Erasmus MC-University Medical Center Rotterdam, Rotterdam, The Netherlands.
Henning TiemeierDepartment of Child and Adolescent Psychiatry/Psychology, Erasmus MC-University Medical Center Rotterdam, Rotterdam, The Netherlands.
Marian J Bakermans-KranenburgCentre for Child and Family Studies, Leiden University, Leiden, The Netherlands.
Erasmus University Rotterdam · NLErasmus MC · NLLeiden University · NL

Funding

European Research Council 648916
6 · The paper itself

Abstract

Findings of studies investigating OXTR SNP rs53576 (G-A) variation in social behavior have been inconsistent, possibly because DNA methylation after stress exposure was eliminated from consideration. Our goal was to examine OXTR rs53576 allele-specific sensitivity for neonatal OXTR DNA methylation in relation to (1) a prenatal maternal stress composite, and (2) child autistic traits. Prospective data from fetal life to age 6 years were collected in a total of 743 children participating in the Generation R Study. Prenatal maternal stress exposure was uniquely associated with child autistic traits but was unrelated to OXTR methylation across both OXTR rs53576 G-allele homozygous children and A-allele carriers. For child autistic traits in general and social communication problems in particular, we observed a significant OXTR rs53576 genotype by OXTR methylation interaction in the absence of main effects, suggesting that opposing effects cancelled each other out. Indeed, OXTR methylation levels were positively associated with social problems for OXTR rs53576 G-allele homozygous children but not for A-allele carriers. These results highlight the importance of incorporating epi-allelic information and support the role of OXTR methylation in child autistic traits. Autism Res 2017, 10: 430-438. © 2016 International Society for Autism Research, Wiley Periodicals, Inc.

Indexed as

Autistic DisorderChildDNA MethylationFemaleGenotypeHumansMaleNetherlandsProspective StudiesReceptors, OxytocinStress, PsychologicalSurveys and QuestionnairesOXTR protein, humanReceptors, Oxytocinautistic traitsDNA methylationoxytocin receptor gene (OXTR)stress exposure

Identifiers

PMID27520745
PMCPMC5426537
OpenAlexW2516940853

What OpenQuestion holds

Textmetadata
LicenceTDM
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.