Evidence map›Paper›PMID 28975925›Full record

ArticleNeuropsychopharmacology : official publication of the American College of Neuropsychopharmacology2018

FKBP5 Moderates the Association between Antenatal Maternal Depressive Symptoms and Neonatal Brain Morphology.

Changqing Wang, Mojun Shen, Bryan Guillaume, Yap-Seng Chong, Helen Chen, Marielle V Fortier, Michael J Meaney, Anqi Qiu

Open access · bronzeAbstract read
In one paragraph

Article in Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed, 2 pooled it
5.0field-weighted citation impact, top 5% 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

21 citing papers in PubMed, 2 syntheses or guidelines pooled it, 50 citations in OpenAlex.

  1. Pooled it
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  16. Inflammatory modulation of the associations between prenatal maternal depression and neonatal brain.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2021
    Article
  17. Article
  18. Maternal care in infancy and the course of limbic development.Developmental cognitive neuroscience · 2019
    Article
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  20. Review
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 2 countries.

Changqing WangDepartment of Biomedical Engineering and Clinical Imaging Research Center, National University of Singapore, Singapore.
Mojun ShenSingapore Institute for Clinical Sciences, Singapore.
Bryan GuillaumeDepartment of Biomedical Engineering and Clinical Imaging Research Center, National University of Singapore, Singapore.
Yap-Seng ChongSingapore Institute for Clinical Sciences, Singapore.
Helen ChenKK Women's and Children's Hospital, Duke-National University of Singapore, Singapore.
Marielle V FortierDepartment of Diagnostic and Interventional Imaging, KK Women's and Children's Hospital (KKH), Singapore.
Michael J MeaneySingapore Institute for Clinical Sciences, Singapore.
Anqi QiuDepartment of Biomedical Engineering and Clinical Imaging Research Center, National University of Singapore, Singapore.ORCID 0000-0002-0215-6338
National University of Singapore · SGDouglas Mental Health University Institute · CAKK Women's and Children's Hospital · SGSingapore Institute for Clinical Sciences · SG

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Antenatal maternal depressive symptoms influence fetal brain development and increase the risk for depression in offspring. Such vulnerability is often moderated by the offspring's genetic variants. This study aimed to examine whether FKBP5, a key regulator of the hypothalamic-pituitary-adrenal (HPA) axis, moderates the association between antenatal maternal depressive symptoms and in utero brain development, using an Asian cohort with 161 mother-offspring dyads. Antenatal maternal depressive symptoms were measured using the Edinburgh Postnatal Depression Scale (EPDS) during the second trimester of pregnancy. Neonatal structural brain images were acquired using magnetic resonance imaging (MRI) shortly after birth. Maternal and neonatal FKBP5 gene was genotyped using Illumina OmniExpress arrays. A gene set-based mixed effect model for gene-environment interaction (MixGE) was used to examine interactive effects between neonatal genetic variants of FKBP5 and antenatal maternal depressive symptoms on neonatal amygdala and hippocampal volumes, and cortical thickness. Our study revealed that genetic variants in neonatal FKBP5 moderate the association between antenatal maternal depressive symptoms and right hippocampal volume but only show a trend for such moderation on amygdala volumes and cortical thickness. Our findings are the first to reveal that the association between maternal depressive symptoms and in utero neurodevelopment of specific brain regions is modified through complex genetic variation in neonatal FKBP5. Our results suggest that an increased risk for depression may be transmitted from mother to child during fetal life and that the effect is dependent upon neonatal FKBP5 genotype.

Indexed as

Pregnancy ComplicationsBrainCohort StudiesDepressionFemaleGene-Environment InteractionHumansInfant, NewbornMagnetic Resonance ImagingMaleOrgan SizePolymorphism, Single NucleotidePregnancyPsychiatric Status Rating ScalesRisk FactorsTacrolimus Binding Protein 5Tacrolimus Binding Protein 5Tacrolimus Binding Proteins

Identifiers

PMID28975925
PMCPMC5770768
OpenAlexW2762228016

What OpenQuestion holds

Textmetadata
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.