Evidence map›Paper›PMID 26765264›Full record

ArticleGenes and immunity2016

The multiple sclerosis susceptibility genes TAGAP and IL2RA are regulated by vitamin D in CD4+ T cells.

T Berge, I S Leikfoss, I S Brorson, S D Bos, C M Page, M W Gustavsen, A Bjølgerud, T Holmøy, E G Celius, J Damoiseaux and 3 more

Open access · hybridAbstract read
In one paragraph

Article in Genes and immunity, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
2.6field-weighted citation impact, top 11% 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

24 citing papers in PubMed, 42 citations in OpenAlex.

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  15. Analysis of Single Nucleotide Polymorphisms inReports of biochemistry & molecular biology · 2020
    Article
  16. Article
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  18. Replication study of GWAS risk loci in Greek multiple sclerosis patients.Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology · 2019
    Article
  19. 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

13 authors at 4 institutions in 2 countries.

T BergeDepartment of Neurology, Oslo University Hospital, Oslo, Norway.
I S LeikfossDepartment of Neurology, Oslo University Hospital, Oslo, Norway.
I S BrorsonDepartment of Neurology, Oslo University Hospital, Oslo, Norway.
S D BosDepartment of Neurology, Oslo University Hospital, Oslo, Norway.
C M PageDepartment of Neurology, Oslo University Hospital, Oslo, Norway.
M W GustavsenDepartment of Neurology, Oslo University Hospital, Oslo, Norway.
A BjølgerudDepartment of Neurology, Oslo University Hospital, Oslo, Norway.
T HolmøyInstitute of Clinical Medicine, University of Oslo, Oslo, Norway.
E G CeliusDepartment of Neurology, Oslo University Hospital, Oslo, Norway.
J DamoiseauxCentral Diagnostic Laboratory, Maastricht University Medical Center, Maastricht, The Netherlands.
J SmoldersDepartment of Neurology, Canisius Wilhelmina Hospital, Nijmegen, The Netherlands.
H F HarboDepartment of Neurology, Oslo University Hospital, Oslo, Norway.
A SpurklandDepartment of Molecular Medicine, Institute of Basic Medical Sciences, University of Oslo, Oslo, Norway.
University of Oslo · NOOslo University Hospital · NOCanisius-Wilhelmina Ziekenhuis · NLMaastricht University · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Multiple sclerosis (MS) is an inflammatory, demyelinating disorder of the central nervous system that develops in genetically susceptible individuals. The majority of the MS-associated gene variants are located in genetic regions with importance for T-cell differentiation. Vitamin D is a potent immunomodulator, and vitamin D deficiency has been suggested to be associated with increased MS disease susceptibility and activity. In CD4+ T cells, we have analyzed in vitro vitamin D responsiveness of genes that contain an MS-associated single-nucleotide polymorphism (SNP) and with one or more vitamin D response elements in their regulatory regions. We identify IL2RA and TAGAP as novel vitamin D target genes. The vitamin D response is observed in samples from both MS patients and controls, and is not dependent on the genotype of MS-associated SNPs in the respective genes.

Indexed as

AdultCD4-Positive T-LymphocytesFemaleGene ExpressionGene Expression ProfilingGenetic Predisposition to DiseaseGTPase-Activating ProteinsHumansInterleukin-2 Receptor alpha SubunitMaleMiddle AgedMultiple SclerosisPolymorphism, Single NucleotidePrimary Cell CultureReceptors, CalcitriolResponse ElementsGTPase-Activating ProteinsIL2RA protein, humanInterleukin-2 Receptor alpha SubunitReceptors, CalcitriolTAGAP protein, humanVDR protein, humanVitamin D

Identifiers

PMID26765264
PMCPMC4783434
OpenAlexW2232860923

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.