Evidence map›Paper›PMID 27523184›Full record

ArticlePsychological medicine2016

Maternal prenatal depression is associated with decreased placental expression of the imprinted gene PEG3.

A B Janssen, L E Capron, K O'Donnell, S J Tunster, P G Ramchandani, A E P Heazell, V Glover, R M John

Open access · hybridAbstract read
In one paragraph

Article in Psychological medicine, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed
5.7field-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

30 citing papers in PubMed, 56 citations in OpenAlex.

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  9. Deficiency of the paternally-expressed imprintedFrontiers in neuroscience · 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

8 authors at 5 institutions in 2 countries.

A B JanssenCardiff School of Biosciences,Cardiff University,Cardiff CF10 3AX,UK.
L E CapronCentre for Mental Health,Imperial College,Hammersmith Campus,London W12 0NN,UK.
K O'DonnellDouglas Mental Health University Institute,6875 La Salle Boulevard,Verdun,Quebec H4H 1R3,Canada.
S J TunsterCardiff School of Biosciences,Cardiff University,Cardiff CF10 3AX,UK.
P G RamchandaniCentre for Mental Health,Imperial College,Hammersmith Campus,London W12 0NN,UK.
A E P HeazellMaternal and Fetal Health Research Centre,University of Manchester,Manchester,UK.
V GloverInstitute of Reproductive and Developmental Biology,Imperial College London,Hammersmith Campus,Du Cane Road,London W12 0NN,UK.
R M JohnCardiff School of Biosciences,Cardiff University,Cardiff CF10 3AX,UK.
Cardiff University · GBCentre for Mental Health · GBDouglas Mental Health University Institute · CAImperial College London · GBUniversity of Manchester · GB

Funding

Persisting Effects of Prenatal Anxiety on Child OutcomesR01MH073842 · NIMH · UNIVERSITY OF ROCHESTER · PI O'CONNOR, THOMAS G · 2006 to 2010
$2.1M
Biotechnology and Biological Sciences Research Council BB/J015156/1Department of Health CS-2013-13-009Medical Research Council MR/M013960/1NIMH NIH HHS R01 MH073842
6 · The paper itself

Abstract

backgroundMaternal prenatal stress during pregnancy is associated with fetal growth restriction and adverse neurodevelopmental outcomes, which may be mediated by impaired placental function. Imprinted genes control fetal growth, placental development, adult behaviour (including maternal behaviour) and placental lactogen production. This study examined whether maternal prenatal depression was associated with aberrant placental expression of the imprinted genes paternally expressed gene 3 (PEG3), paternally expressed gene 10 (PEG10), pleckstrin homology-like domain family a member 2 (PHLDA2) and cyclin-dependent kinase inhibitor 1C (CDKN1C), and resulting impaired placental human placental lactogen (hPL) expression.

methodA diagnosis of depression during pregnancy was recorded from Manchester cohort participants' medical notes (n = 75). Queen Charlotte's (n = 40) and My Baby and Me study (MBAM) (n = 81) cohort participants completed the Edinburgh Postnatal Depression Scale self-rating psychometric questionnaire. Villous trophoblast tissue samples were analysed for gene expression.

resultsIn a pilot study, diagnosed depression during pregnancy was associated with a significant reduction in placental PEG3 expression (41%, p = 0.02). In two further independent cohorts, the Queen Charlotte's and MBAM cohorts, placental PEG3 expression was also inversely associated with maternal depression scores, an association that was significant in male but not female placentas. Finally, hPL expression was significantly decreased in women with clinically diagnosed depression (44%, p < 0.05) and in those with high depression scores (31% and 21%, respectively).

conclusionsThis study provides the first evidence that maternal prenatal depression is associated with changes in the placental expression of PEG3, co-incident with decreased expression of hPL. This aberrant placental gene expression could provide a possible mechanistic explanation for the co-occurrence of maternal depression, fetal growth restriction, impaired maternal behaviour and poorer offspring outcomes.

Indexed as

AdultCohort StudiesDepressionEnglandFemaleGene ExpressionGenomic ImprintingHumansKruppel-Like Transcription FactorsPlacentaPlacental LactogenPregnancyPregnancy ComplicationsSex FactorsKruppel-Like Transcription FactorsPEG3 protein, humanPlacental LactogenHuman placental lactogenPEG3prenatal depression

Identifiers

PMID27523184
PMCPMC5080674
OpenAlexW2513703067

What OpenQuestion holds

Textmetadata
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.