Evidence map›Paper›PMID 32688365›Full record

ArticleNeuropsychopharmacology : official publication of the American College of Neuropsychopharmacology2021

Inflammatory modulation of the associations between prenatal maternal depression and neonatal brain.

Yonghui Wu, Han Zhang, Changqing Wang, Birit F P Broekman, Yap-Seng Chong, Lynette P Shek, Peter D Gluckman, Michael J Meaney, Marielle V Fortier, Anqi Qiu

Open access · hybridAbstract read
In one paragraph

Article in Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed, 2 pooled it
2.5field-weighted citation impact, top 10% 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

16 citing papers in PubMed, 2 syntheses or guidelines pooled it, 27 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

10 authors at 3 institutions in 2 countries.

Yonghui WuDepartment of Biomedical Engineering, National University of Singapore, Singapore, Singapore.
Han ZhangDepartment of Biomedical Engineering, National University of Singapore, Singapore, Singapore.ORCID http://orcid.org/0000-0002-9348-6104
Changqing WangDepartment of Biomedical Engineering, National University of Singapore, Singapore, Singapore.
Birit F P BroekmanSingapore Institute for Clinical Sciences, Singapore, Singapore.
Yap-Seng ChongSingapore Institute for Clinical Sciences, Singapore, Singapore.
Lynette P ShekDepartment of Pediatrics, Khoo Teck Puat - National University Children's Medical Institute, National University of Singapore, Singapore, Singapore.
Peter D GluckmanSingapore Institute for Clinical Sciences, Singapore, Singapore.
Michael J MeaneySingapore Institute for Clinical Sciences, Singapore, Singapore.
Marielle V FortierDepartment of Diagnostic and Interventional Imaging, KK Women's and Children's Hospital, Singapore, Singapore.
Anqi QiuDepartment of Biomedical Engineering, National University of Singapore, Singapore, Singapore. bieqa@nus.edu.sg.ORCID http://orcid.org/0000-0002-0215-6338
National University of Singapore · SGSingapore Institute for Clinical Sciences · SGKK Women's and Children's Hospital · SG

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Inflammatory signaling has a role in sensing intrauterine environment, which may be moderators in altering fetal brain development upon maternal environment. This study integrated cytokine transcriptome of post-mortem fetal brains, neonatal brain imaging and genetic variants (n = 161) to examine whether cytokines are candidates for modulating the relationship between prenatal maternal depression and fetal brain development. This study obtained the transcriptome data of 208 cytokine genes in 12 fetal brain regions from the BrainSpan database. We also included 161 mother-child dyads with prenatal maternal depressive symptoms assessed at 26 weeks of gestation, cytokine genotype data extracted from umbilical cord specimens, and neonatal brain images from a longitudinal prospective birth cohort. We revealed that 22 cytokine genes are expressed in specific brain regions in utero, whose variants have roles in modulating the effects of the prenatal environment on the accelerated fetal development of the hippocampus, auditory, parietal, orbitofrontal, and dorsal prefrontal cortex. Neonates high in the genetic expression score (GES) of TNFRSF19 and IL17RB showed a larger right hippocampal volume, high in the GES of BMPR1B showed the thicker thickness of the sensorimotor cortex, and high in the GES of IL1RAP and CXCR4 demonstrated the thicker thickness of the dorsal and orbital prefrontal cortex in relation with greater prenatal maternal depressive symptoms. Our findings suggest that in humans, the cytokine genes are expressed in a brain region-specific manner in utero and may have potential roles in modulating the fetal development of the corresponding brain regions in response to the maternal environment.

Indexed as

DepressionPrenatal Exposure Delayed EffectsBrainChildFemaleFetal DevelopmentHumansInfant, NewbornMagnetic Resonance ImagingPregnancyProspective StudiesReceptors, Tumor Necrosis FactorReceptors, Tumor Necrosis FactorTNFRSF19 protein, human

Identifiers

PMID32688365
PMCPMC7852623
OpenAlexW3042771326

What OpenQuestion holds

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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.