Evidence map›Paper›PMID 26686848›Full record

ArticleMolecular biology reports2016

Vitamin D receptor polymorphisms and expression profile in rheumatoid arthritis Brazilian patients.

Catarina Addobbati Jordão Cavalcanti, Jaqueline de Azevêdo Silva, Will de Barros Pita, Tiago Degani Veit, Odirlei Andre Monticielo, Ricardo Machado Xavier, João Carlos Tavares Brenol, Cleiton Viegas Brenol, Thiago Sotero Fragoso, Alexandre Domingues Barbosa and 7 more

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In one paragraph

Article in Molecular biology reports, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed, 2 pooled it
1.8field-weighted citation impact, top 16% 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

10 citing papers in PubMed, 2 syntheses or guidelines pooled it, 17 citations in OpenAlex.

  1. Association between VDR polymorphisms and multiple sclerosis: systematic review and updated meta-analysis of case-control studies.Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology · 2018
    Pooled it
  2. Pooled it
  3. Article
  4. Article
  5. Article
  6. Article
  7. Atherosclerosis in Rheumatoid Arthritis: Promoters and Opponents.Clinical reviews in allergy & immunology · 2020
    Review
  8. Article
  9. Is Nasal Polyposis Related to Levels of Serum Vitamin D and Vitamin D Receptor Gene Expression?Medical science monitor : international medical journal of experimental and clinical research · 2016
    Article
  10. 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

17 authors at 4 institutions in 1 country.

Catarina Addobbati Jordão CavalcantiDepartment of Genetics, Federal University of Pernambuco, Recife, Pernambuco, Brazil.
Jaqueline de Azevêdo SilvaLaboratory of Immunopathology Keizo Asami (LIKA), Federal University of Pernambuco, Av. Moraes Rego, 1235, CEP 50760-901, Recife, Pernambuco, Brazil. j.azvedo@gmail.com.
Will de Barros PitaDepartment of Antibiotics, Federal University of Pernambuco, Recife, Pernambuco, Brazil.
Tiago Degani VeitDepartment of Genetics, Federal University of Rio Grande do Sul, Porto Alegre, Rio Grande do Sul, Brazil.
Odirlei Andre MonticieloDivision of Rheumatology, Clinical Hospital, Federal University of Rio Grande do Sul, Porto Alegre, Brazil.
Ricardo Machado XavierDivision of Rheumatology, Clinical Hospital, Federal University of Rio Grande do Sul, Porto Alegre, Brazil.
João Carlos Tavares BrenolDivision of Rheumatology, Clinical Hospital, Federal University of Rio Grande do Sul, Porto Alegre, Brazil.
Cleiton Viegas BrenolDivision of Rheumatology, Clinical Hospital, Federal University of Rio Grande do Sul, Porto Alegre, Brazil.
Thiago Sotero FragosoRheumatology Service, Clinical Hospital, Federal University of Alagoas, Maceió, Alagoas, Brazil.
Alexandre Domingues BarbosaRheumatology Division, Clinical Hospital, Federal University of Pernambuco, Recife, Pernambuco, Brazil.
Ângela Luiza Branco Pinto DuarteRheumatology Division, Clinical Hospital, Federal University of Pernambuco, Recife, Pernambuco, Brazil.
Renê Donizeti Ribeiro OliveiraClinical Immunology Division, Department of Medicine, Medicine Faculty of Ribeirão Preto, University of São Paulo, Ribeirão Preto, São Paulo, Brazil.
Paulo Louzada-JúniorClinical Immunology Division, Department of Medicine, Medicine Faculty of Ribeirão Preto, University of São Paulo, Ribeirão Preto, São Paulo, Brazil.
Eduardo Antônio DonadiClinical Immunology Division, Department of Medicine, Medicine Faculty of Ribeirão Preto, University of São Paulo, Ribeirão Preto, São Paulo, Brazil.
Sergio CrovellaDepartment of Genetics, Federal University of Pernambuco, Recife, Pernambuco, Brazil.
José Artur Bogo ChiesDepartment of Genetics, Federal University of Rio Grande do Sul, Porto Alegre, Rio Grande do Sul, Brazil.
Paula Sandrin-GarciaDepartment of Genetics, Federal University of Pernambuco, Recife, Pernambuco, Brazil.
Universidade Federal de Pernambuco · BRUniversidade Federal do Rio Grande do Sul · BRUniversidade de São Paulo · BRUniversidade Federal de Alagoas · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Rheumatoid arthritis (RA) is an autoimmune disease characterized by chronic inflammation and important joint commitment, being the most common systemic autoimmune disease worldwide. RA displays important genetic background with a variety of genes contributing to the immune balance breakdown. Recent studies have demonstrated that vitamin D, through its receptor (VDR), is able to regulate the immune balance and suppress the autoimmunity process, being a potential target in autoimmune diseases. In the present genetic association study, we assessed 5 Tag single nucleotide polymorphisms (SNPs) (rs11168268, rs2248098, rs1540339, rs4760648 and rs3890733), which cover most of the VDR gene, in three different Brazilian populations (from Northeast, Southeast and South Brazil). We also evaluated the VDR expression profile in whole blood and monocytes from RA patients. For genotyping study, 428 RA patients and 616 healthy controls were genotyped with fluorogenic allele specific probes on an ABI7500 platform. For gene expression study, VDR mRNA levels of 15 RA patients and 26 healthy individuals were assessed by RT-PCR. Our results showed that SNPs rs4760648 and rs3890733 are associated to RA susceptibility (p value = 0.0026, OR 1.31 and p value = 0.0091, OR 1.28 with statistical power = 0.999 and 0.993, respectively). Regarding RA clinical features, the studied SNPs did not show significant associations. The gene expression assays showed that VDR mRNA levels were down regulated in both whole blood (-3.3 fold) and monocytes (-3.2 fold) of RA patients when compared to healthy controls. Our results, the first reported for distinct Brazilian populations, support a role of the VDR gene in the susceptibility to RA.

Indexed as

AllelesArthritis, RheumatoidBrazilCase-Control StudiesFemaleGenetic Predisposition to DiseaseHumansMaleMiddle AgedPolymorphism, Single NucleotideReceptors, CalcitriolReceptors, CalcitriolVDR protein, humanMonocytesmRNARheumatoid arthritisSNPsVDR

Identifiers

PMID26686848
OpenAlexW2212888825

What OpenQuestion holds

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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.