Evidence map›Paper›PMID 22738990›Full record

ArticleToxicological sciences : an official journal of the Society of Toxicology2012

Toxicogenomic profiles in relation to maternal immunotoxic exposure and immune functionality in newborns.

Kevin Hochstenbach, D M van Leeuwen, H Gmuender, R W Gottschalk, S B Stølevik, U C Nygaard, M Løvik, B Granum, E Namork, H M Meltzer and 3 more

Open access · bronzeAbstract read
In one paragraph

Article in Toxicological sciences : an official journal of the Society of Toxicology, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed, 1 pooled it
9.4field-weighted citation impact, top 2% 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, 1 synthesis or guideline pooled it, 60 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Review
  4. Article
  5. Review
  6. Gene×environment interactions in autism spectrum disorders.Current topics in developmental biology · 2023
    Review
  7. Review
  8. DNA Methylation Patterns inEnvironmental health perspectives · 2021
    Article
  9. Article
  10. Article
  11. Early life exposures shape the CD4Scientific reports · 2019
    Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. Article
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 at 3 institutions in 3 countries.

Kevin HochstenbachDepartment of Toxicogenomics, Maastricht University, Maastricht, The Netherlands.
D M van Leeuwen
H Gmuender
R W Gottschalk
S B Stølevik
U C Nygaard
M Løvik
B Granum
E Namork
H M Meltzer
J C Kleinjans
J H M van Delft
Henk van Loveren
Norwegian Institute of Public Health · NOMaastricht University · NLGenedata (Switzerland) · CH

Funding

Gene-Environment Interactions in an Autism Birth CohortU01NS047537 · NINDS · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI LIPKIN, W. IAN · 2003 to 2013
$27.0M
NIEHS NIH HHS N0-ES-75558NINDS NIH HHS 1UO1 NS 047537-01
6 · The paper itself

Abstract

A crucial period for the development of the immune system occurs in utero. This results in a high fetal vulnerability to immunotoxic exposure, and indeed, immunotoxic effects have been reported, demonstrating negative effects on immune-related health outcomes and immune functionality. Within the NewGeneris cohort BraMat, a subcohort of the Norwegian Mother and Child Cohort Study (MoBa), immunotoxicity was demonstrated for polychlorinated biphenyls and dioxins, showing associations between estimated maternal intake levels and reduced measles vaccination responses in the offspring at the age of 3. The present study aimed to investigate this link at the transcriptomic level within the same BraMat cohort. To this end, whole-genome gene expression in cord blood was investigated and found to be associated with maternal Food Frequency Questionnaires-derived exposure estimates and with vaccination responses in children at 3 years of age. Because the literature reports gender specificity in the innate, humoral, and cell-mediated responses to viral vaccines, separate analysis for males and females was conducted. Separate gene sets for male and female neonates were identified, comprising genes significantly correlating with both 2,3,7,8-tetrachlorodibenzodioxin (TCDD) and polychlorinated biphenyls (PCB) exposure and with measles vaccination response. Noteworthy, genes correlating negatively with exposure in general show positive correlations with antibody levels and vice versa. For both sexes, these included immune-related genes, suggesting immunosuppressive effects of maternal exposure to TCDD and PCB at the transcriptomic level in neonates in relation to measles vaccination response 3 years later.

Indexed as

Maternal ExposurePharmacogeneticsCohort StudiesDiet RecordsFemaleHumansImmunotoxinsInfant, NewbornMaleMeasles VaccinePolychlorinated BiphenylsPolychlorinated DibenzodioxinsPregnancySurveys and QuestionnairesTranscriptomeImmunotoxinsMeasles VaccinePolychlorinated BiphenylsPolychlorinated Dibenzodioxins

Identifiers

PMID22738990
PMCPMC3529642
OpenAlexW2136385490

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.