Evidence map›Paper›PMID 26121239›Full record

ArticlePloS one2015

Vitamin D Receptor Gene Ablation in the Conceptus Has Limited Effects on Placental Morphology, Function and Pregnancy Outcome.

Rebecca L Wilson, Sam Buckberry, Fleur Spronk, Jessica A Laurence, Shalem Leemaqz, Sean O'Leary, Tina Bianco-Miotto, Jing Du, Paul H Anderson, Claire T Roberts

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
2.0field-weighted citation impact, top 15% 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

13 citing papers in PubMed, 27 citations in OpenAlex.

  1. Article
  2. Review
  3. Insight of Autophagy in Spontaneous Miscarriage.International journal of biological sciences · 2022
    Review
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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.

Rebecca L WilsonRobinson Research Institute, Adelaide, Australia; School of Paediatrics and Reproductive Health, University of Adelaide, Adelaide, Australia.
Sam BuckberryRobinson Research Institute, Adelaide, Australia; School of Paediatrics and Reproductive Health, University of Adelaide, Adelaide, Australia.
Fleur SpronkRobinson Research Institute, Adelaide, Australia; School of Paediatrics and Reproductive Health, University of Adelaide, Adelaide, Australia.
Jessica A LaurenceRobinson Research Institute, Adelaide, Australia; School of Paediatrics and Reproductive Health, University of Adelaide, Adelaide, Australia.
Shalem LeemaqzRobinson Research Institute, Adelaide, Australia; School of Paediatrics and Reproductive Health, University of Adelaide, Adelaide, Australia.
Sean O'LearyRobinson Research Institute, Adelaide, Australia; School of Paediatrics and Reproductive Health, University of Adelaide, Adelaide, Australia.
Tina Bianco-MiottoRobinson Research Institute, Adelaide, Australia; School of Agriculture, Food and Wine, University of Adelaide, Adelaide, Australia.
Jing DuRobinson Research Institute, Adelaide, Australia; Shanghai Institute of Planned Parenthood Research, Shanghai, China.
Paul H AndersonSchool of Pharmacy and Medical Sciences, Division of Health Sciences, University of South Australia, Adelaide, Australia.
Claire T RobertsRobinson Research Institute, Adelaide, Australia; School of Paediatrics and Reproductive Health, University of Adelaide, Adelaide, Australia.
University of Adelaide · AUShanghai Institute of Planned Parenthood Research · CNUniversity of South Australia · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Vitamin D deficiency has been implicated in the pathogenesis of several pregnancy complications attributed to impaired or abnormal placental function, but there are few clues indicating the mechanistic role of vitamin D in their pathogenesis. To further understand the role of vitamin D receptor (VDR)-mediated activity in placental function, we used heterozygous Vdr ablated C57Bl6 mice to assess fetal growth, morphological parameters and global gene expression in Vdr null placentae. Twelve Vdr+/- dams were mated at 10-12 weeks of age with Vdr+/- males. At day 18.5 of the 19.5 day gestation in our colony, females were euthanised and placental and fetal samples were collected, weighed and subsequently genotyped as either Vdr+/+, Vdr+/- or Vdr-/-. Morphological assessment of placentae using immunohistochemistry was performed and RNA was extracted and subject to microarray analysis. This revealed 25 genes that were significantly differentially expressed between Vdr+/+ and Vdr-/- placentae. The greatest difference was a 6.47-fold change in expression of Cyp24a1 which was significantly lower in the Vdr-/- placentae (P<0.01). Other differentially expressed genes in Vdr-/- placentae included those involved in RNA modification (Snord123), autophagy (Atg4b), cytoskeletal modification (Shroom4), cell signalling (Plscr1, Pex5) and mammalian target of rapamycin (mTOR) signalling (Deptor and Prr5). Interrogation of the upstream sequence of differentially expressed genes identified that many contain putative vitamin D receptor elements (VDREs). Despite the gene expression differences, this did not contribute to any differences in overall placental morphology, nor was function affected as there was no difference in fetal growth as determined by fetal weight near term. Given our dams still expressed a functional VDR gene, our results suggest that cross-talk between the maternal decidua and the placenta, as well as maternal vitamin D status, may be more important in determining pregnancy outcome than conceptus expression of VDR.

Indexed as

Gene DeletionAnimalsFemaleFetusGene Expression ProfilingGenotypeIntracellular Signaling Peptides and ProteinsMaleMice, Inbred C57BLOligonucleotide Array Sequence AnalysisPlacentaPregnancyPregnancy OutcomeReal-Time Polymerase Chain ReactionReceptors, CalcitriolReproducibility of Resultsdeptor protein, mouseIntracellular Signaling Peptides and ProteinsReceptors, CalcitriolVitamin D3 24-Hydroxylase

Identifiers

PMID26121239
PMCPMC4488298
OpenAlexW1533442501

What OpenQuestion holds

Textmetadata
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.