Evidence map›Paper›PMID 27244231›Full record

ArticleTranslational psychiatry2016

Prenatal immune programming of the sex-dependent risk for major depression.

S E Gilman, S Cherkerzian, S L Buka, J Hahn, M Hornig, J M Goldstein

Open access · goldAbstract read
In one paragraph

Article in Translational psychiatry, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 53 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
53citing papers in PubMed, 1 pooled it
4.1field-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

53 citing papers in PubMed, 1 synthesis or guideline pooled it, 78 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Socioeconomic disadvantage, gestational immune activity, and neurodevelopment in early childhood.Proceedings of the National Academy of Sciences of the United States of America · 2017
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  6. Impacts of prenatal resiquimod exposure during late gestation on rat offspring development and behavior.American journal of physiology. Regulatory, integrative and comparative physiology · 2026
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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

6 authors at 4 institutions in 1 country.

S E GilmanHealth Behavior Branch, Division of Intramural Population Health Research, Eunice Kennedy Shriver National Institute of Child Health and Human Development, Rockville, MD, USA.
S CherkerzianConnors Center for Women's Health and Gender Biology, Boston, MA, USA.
S L BukaDepartment of Epidemiology, Brown University School of Public Health, Providence, RI, USA.
J HahnDepartment of Social and Behavioral Sciences, Harvard T. H. Chan School of Public Health, Boston, MA, USA.
M HornigCenter for Infection and Immunity, Columbia University Mailman School of Public Health, New York, NY, USA.
J M GoldsteinConnors Center for Women's Health and Gender Biology, Boston, MA, USA.
Harvard University · USBrown University · USColumbia University · USEunice Kennedy Shriver National Institute of Child Health and Human Development · US

Funding

Sex-Specific Programming of the HPA Axis by GlucocorticoidsP50MH082679 · NIMH · BRIGHAM AND WOMEN'S HOSPITAL · PI GOLDSTEIN, JILL M · 2007 to 2011
$5.9M
Fetal Antecedents to Depression and Risk for CVDR01MH074679 · NIMH · BRIGHAM AND WOMEN'S HOSPITAL · PI GOLDSTEIN, JILL M · 2007 to 2011
$3.7M
Fetal Hormonal Programming of Sex Differences in Aging of the Memory CircuitryR01MH090291 · NIMH · BRIGHAM AND WOMEN'S HOSPITAL · PI GOLDSTEIN, JILL M · 2011 to 2015
$3.5M
Social Imprinting in the Development of Major DepressionR01MH087544 · NIMH · HARVARD SCHOOL OF PUBLIC HEALTH · PI GILMAN, STEPHEN E · 2009 to 2012
$1.3M
Maternal immune activity during pregnancy and offspring neurodevelomentZIAHD008961 · NICHD · EUNICE KENNEDY SHRIVER NATIONAL INSTITUTE OF CHILD HEALTH & HUMAN DEVELOPMENT · PI GILMAN, STEPHEN · 2017 to 2017
$134k
NIMH NIH HHS P50 MH082679NIMH NIH HHS R01 MH074679NIMH NIH HHS R01 MH087544NIMH NIH HHS R01 MH090291
6 · The paper itself

Abstract

Maternal immune functioning during pregnancy contributes to sex-dependent deficits in neurodevelopment and to behaviors associated with affective traits in preclinical studies, and has been indirectly associated with offspring depression in epidemiologic studies. We therefore investigated the association between immune activity during pregnancy and the risk of depression among male and female offspring. We conducted a case-control study of depression (n=484 cases and n=774 controls) using data from the New England Family Study, a pregnancy cohort enrolled between 1959 and 1966 that assessed psychiatric outcomes in adult offspring (mean age=39.7 years). We assayed concentrations of three pro-inflammatory cytokines, interleukin (IL)-1β, IL-6 and tumor necrosis factor (TNF)-α, and the anti-inflammatory cytokine, IL-10, in maternal serum collected at the end of the second and beginning of the third trimesters. High maternal TNF-α was associated with reduced odds of depression among both male and female offspring (odds ratio (OR)=0.68; confidence interval (CI)=0.48, 0.98). However, when considering the TNF-α to IL-10 ratio, a measure of the ratio of pro- to anti-inflammatory loading, maternal immune effects on offspring depression differed significantly by sex (χ(2)=13.9, degrees of freedom=4, P=0.008). Among females, higher maternal TNF-α:IL-10 was associated with reduced odds of depression (OR=0.51; CI=0.32, 0.81), whereas, among males, high maternal TNF-α:IL-10 was associated with elevated odds of depression (OR=1.86; CI=1.02, 3.39). Thus, the balance between TNF-α and IL-10 in maternal prenatal serum was associated with depression in a sex-dependent manner. These findings are consistent with the role of TNF-α in the maturation of the sexually dimorphic fetal brain circuitry that regulates stress and affective responses, and support a prenatal stress-immune model of depression pathogenesis.

Indexed as

AdolescentAdult ChildrenCase-Control StudiesCohort StudiesFemaleHumansInfant, NewbornInflammation MediatorsInterleukin-10Major Depressive DisorderMaleNeurodevelopmental DisordersPregnancyPregnancy ComplicationsPrenatal Exposure Delayed EffectsRisk FactorsIL10 protein, humanInflammation MediatorsInterleukin-10

Identifiers

PMID27244231
PMCPMC5545649
OpenAlexW2410741141

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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.