Evidence map›Paper›PMID 26784953›Full record

ArticlePloS one2016

Genetic Variation in the REL Gene Increases Risk of Behcet's Disease in a Chinese Han Population but That of PRKCQ Does Not.

Feilan Chen, Lei Xu, Tingting Zhao, Xiang Xiao, Yongquan Pan, Shengping Hou

Open access · goldAbstract readComparative Study
In one paragraph

Article in PloS one, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
2.4field-weighted citation impact, top 13% 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

8 citing papers in PubMed, 13 citations in OpenAlex.

  1. The Role ofInternational journal of molecular sciences · 2026
    Article
  2. The Immunogenetics of Behcet's Disease.Advances in experimental medicine and biology · 2022
    Article
  3. Review
  4. Molecular vision · 2019
    Article
  5. Association ofThe British journal of ophthalmology · 2018
    Article
  6. Review
  7. Review
  8. 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

6 authors at 2 institutions in 1 country.

Feilan ChenChongqing Medical University, Chongqing, P. R. China.
Lei XuChongqing Medical University, Chongqing, P. R. China.
Tingting ZhaoChongqing Medical University, Chongqing, P. R. China.
Xiang XiaoThe First Affiliated Hospital of Chongqing Medical University, Chongqing, P. R. China.
Yongquan PanChongqing Medical University, Chongqing, P. R. China.
Shengping HouThe First Affiliated Hospital of Chongqing Medical University, Chongqing, P. R. China.
Chongqing Academy of Animal Science · CNFirst Affiliated Hospital of Chongqing Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Genome-wide association studies (GWAS) and candidate gene studies have identified the REL and PRKCQ genes as risk loci for various autoimmune diseases. The purpose of the present study was to investigate the association of the REL and PRKCQ genes with Behcet's disease (BD) in a Chinese Han population. A case-control study was conducted on three single nucleotide polymorphisms (SNPs), rs13031237, rs702873, and rs842647 of the REL gene and three SNPs (rs4750316, rs11258747, and rs947474) of the PRKCQ gene using polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) in a total of 623 BD patients and 1,074 healthy controls. Multiple variables were assessed, including age, sex distribution, and extra-ocular findings. In the present study, the frequencies of rs842647 GG genotypes and rs842647 G alleles were significantly higher in patients than in controls and those of the rs842647 AG genotypes were lower in patients than in controls [GG genotype: Bonferroni corrected P-value for gender adjustment (Pc(a)) = 0.0074, odds ratio (OR) = 1.63; G allele: Pc(a) = 0.0072, OR = 1.57; AG genotype: Pc(a) = 0.024, OR = 0.63, respectively]. No statistically significant differences in the frequencies of rs702873, rs13031237, rs4750316, rs11258747, and rs947474 between BD patients and controls were observed. Stratification analysis indicated that the REL rs842647 polymorphism was associated with BD patients with skin lesions. No significant association of the other five SNPs between BD patients with other extra-ocular findings, including genital ulcer, arthritis, and positive pathergy test results was found. The REL rs842647 polymorphism may be a susceptibility factor for BD pathogenesis and skin lesions, which indicate that c-Rel may be involved in the pathogenesis and skin lesions of BD through the NF-κB pathway.

Indexed as

Genetic Predisposition to DiseaseAdultBehcet SyndromeCase-Control StudiesChinaFemaleGenome-Wide Association StudyGenotypeHumansIsoenzymesMalePolymerase Chain ReactionPolymorphism, Restriction Fragment LengthPolymorphism, Single NucleotideProtein Kinase CProtein Kinase C-thetaIsoenzymesPRKCQ protein, humanProtein Kinase CProtein Kinase C-thetaProto-Oncogene Proteins c-rel

Identifiers

PMID26784953
PMCPMC4718718
OpenAlexW2271908071

What OpenQuestion holds

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LicenceCC BY
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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.