Evidence map›Paper›PMID 28686601›Full record

ArticlePloS one2017

Maternal and neonatal vitamin D status, genotype and childhood celiac disease.

Karl Mårild, German Tapia, Margareta Haugen, Sandra R Dahl, Arieh S Cohen, Marika Lundqvist, Benedicte A Lie, Lars C Stene, Ketil Størdal

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed, 2 pooled it
3.3field-weighted citation impact, top 7% 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

20 citing papers in PubMed, 2 syntheses or guidelines pooled it, 33 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
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  4. Review
  5. Article
  6. Assessment of the contribution ofJournal of genetics · 2024
    Article
  7. Review
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  11. Article
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  14. Article
  15. A Comprehensive Review of Celiac Disease/Gluten-Sensitive Enteropathies.Clinical reviews in allergy & immunology · 2019
    Review
  16. Article
  17. Review
  18. Review
  19. Review
  20. Fetal and Maternal Genetic Variants Influencing Neonatal Vitamin D Status.The Journal of clinical endocrinology and metabolism · 2017
    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

9 authors at 3 institutions in 2 countries.

Karl MårildNorwegian Institute of Public Health, Oslo, Norway.
German TapiaNorwegian Institute of Public Health, Oslo, Norway.
Margareta HaugenNorwegian Institute of Public Health, Oslo, Norway.
Sandra R DahlAker Hormone Laboratory, Oslo University Hospital, Oslo, Norway.
Arieh S CohenDanish Center for newborn screening, Statens Serum Institut, Copenhagen, Denmark.
Marika LundqvistDanish Center for newborn screening, Statens Serum Institut, Copenhagen, Denmark.
Benedicte A LieDepartment of Medical Genetics, University of Oslo and Oslo University Hospital, Oslo, Norway.
Lars C SteneNorwegian Institute of Public Health, Oslo, Norway.
Ketil StørdalNorwegian Institute of Public Health, Oslo, Norway.ORCID http://orcid.org/0000-0001-7826-8646
Norwegian Institute of Public Health · NOOslo University Hospital · NOStatens Serum Institut · DK

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 N01 ES075558NINDS NIH HHS U01 NS047537
6 · The paper itself

Abstract

backgroundLow concentration of 25-hydroxyvitamin D during pregnancy may be associated with offspring autoimmune disorders. Little is known about environmental triggers except gluten for celiac disease, a common immune-mediated disorder where seasonality of birth has been reported as a risk factor. We therefore aimed to test whether low maternal and neonatal 25-hydroxyvitamin D predicted higher risk of childhood celiac disease. METHODS AND

findingsIn this Norwegian nationwide pregnancy cohort (n = 113,053) and nested case-control study, we analyzed 25-hydroxyvitamin D in maternal blood from mid-pregnancy, postpartum and cord plasma of 416 children who developed celiac disease and 570 randomly selected controls. Mothers and children were genotyped for established celiac disease and vitamin D metabolism variants. We used mixed linear regression models and logistic regression to study associations. There was no significant difference in average 25-hydroxyvitamin D between cases and controls (63.1 and 62.1 nmol/l, respectively, p = 0.28), and no significant linear trend (adjusted odds ratio per 10 nM increase 1.05, 95% CI: 0.93-1.17). Results were similar when analyzing the mid-pregnancy, postpartum or cord plasma separately. Genetic variants for vitamin D deficiency were not associated with celiac disease (odds ratio per risk allele of the child, 1.00; 95% CI, 0.90 to 1.10, odds ratio per risk allele of the mother 0.94; 95% CI 0.85 to 1.04). Vitamin D intake in pregnancy or by the child in early life did not predict later celiac disease. Adjustment for established genetic risk markers for celiac disease gave similar results.

conclusionsWe found no support for the hypothesis that maternal or neonatal vitamin D status is related to the risk of childhood celiac disease.

Indexed as

AdultCeliac DiseaseChildFemaleGenotypeHumansInfantMaleMaternal Nutritional Physiological PhenomenaPregnancyPregnancy ComplicationsRisk FactorsVitamin DVitamin D DeficiencyVitamin D

Identifiers

PMID28686601
PMCPMC5501391
OpenAlexW2731790019

What OpenQuestion holds

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LicenceCC BY
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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.