Evidence map›Paper›PMID 30068408›Full record

ArticleDevelopment and psychopathology2018

Inflammation-related epigenetic risk and child and adolescent mental health: A prospective study from pregnancy to middle adolescence.

Edward D Barker, Charlotte A M Cecil, Esther Walton, Lotte C Houtepen, Thomas G O'Connor, Andrea Danese, Sara R Jaffee, Sarah K G Jensen, Carmine Pariante, Wendy McArdle and 3 more

Abstract read
In one paragraph

Article in Development and psychopathology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed, 2 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

35 citing papers in PubMed, 2 syntheses or guidelines pooled it.

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  18. Associations of DNA-methylation measures of biological aging with social disparities in child and adolescent mental health.Clinical psychological science : a journal of the Association for Psychological Science · 2024
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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

13 authors.

Edward D BarkerKing's College London.
Charlotte A M CecilKing's College London.
Esther WaltonUniversity of Bristol.
Lotte C HoutepenUniversity of Bristol.
Thomas G O'ConnorUniversity of Rochester Medical Center.
Andrea DaneseKing's College London.
Sara R JaffeeUniversity of Pennsylvania.
Sarah K G JensenHarvard University Medical School.
Carmine ParianteKing's College London.
Wendy McArdleUniversity of Bristol.
Tom R GauntUniversity of Bristol.
Caroline L ReltonUniversity of Bristol.
Susanna RobertsKing's College London.

Funding

Epigenetic Pathways to Conduct Problem Trajectories: Early Environmental RisksR01HD068437 · NICHD · KING'S COLLEGE LONDON · PI BARKER, EDWARD D., MILL, JONATHAN · 2012 to 2014
$1.1M
Biotechnology and Biological Sciences Research Council BB/I025263/1Biotechnology and Biological Sciences Research Council BBI025751/1Medical Research Council G108/603Medical Research Council MC_PC_15018Medical Research Council MC_UU_00011/4Medical Research Council MC_UU_12013/2Medical Research Council MC_UU_12013/8Medical Research Council MR/J002739/1Medical Research Council MR/N029488/1NICHD NIH HHS R01 HD068437Wellcome TrustWellcome Trust 02215/2/13/2
6 · The paper itself

Abstract

In 785 mother-child (50% male) pairs from a longitudinal epidemiological birth cohort, we investigated associations between inflammation-related epigenetic polygenic risk scores (i-ePGS), environmental exposures, cognitive function, and child and adolescent internalizing and externalizing problems. We examined prenatal and postnatal effects. For externalizing problems, one prenatal effect was found: i-ePGS at birth associated with higher externalizing problems (ages 7-15) indirectly through lower cognitive function (age 7). For internalizing problems, we identified two effects. For a prenatal effect, i-ePGS at birth associated with higher internalizing symptoms via continuity in i-ePGS at age 7. For a postnatal effect, higher postnatal adversity exposure (birth through age 7) associated with higher internalizing problems (ages 7-15) via higher i-ePGS (age 7). Hence, externalizing problems were related mainly to prenatal effects involving lower cognitive function, whereas internalizing problems appeared related to both prenatal and postnatal effects. The present study supports a link between i-ePGS and child and adolescent mental health.

Indexed as

Mental HealthAdolescentChildChild Behavior DisordersFemaleHumansInflammationMalePregnancyProspective StudiesRisk Factors

Identifiers

PMID30068408
PMCPMC7612578

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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.