Evidence map›Paper›PMID 18769923›Full record

ArticleRheumatology international2008

Interleukin-17F gene polymorphisms in Korean patients with Behçet's disease.

Won-Cheoul Jang, Yun-Hyoung Nam, Young-Chang Ahn, Sang-Hyun Lee, Sung-Hoon Park, Jung-Yoon Choe, Shin-Seok Lee, Seong-Kyu Kim

Abstract read
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Article in Rheumatology international, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
4.4field-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

18 citing papers in PubMed, 55 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Review
  5. Article
  6. Article
  7. Article
  8. Article
  9. Review
  10. Article
  11. Genetic polymorphisms of interleukin 17A and interleukin 17F and their association with inflammatory bowel disease in a Chinese Han population.Inflammation research : official journal of the European Histamine Research Society ... [et al.] · 2013
    Article
  12. Article
  13. Article
  14. Article
  15. Genetics of Behçet's Disease.Pathology research international · 2012
    Article
  16. Cytokines in autoimmune uveitis.Journal of interferon & cytokine research : the official journal of the International Society for Interferon and Cytokine Research · 2011
    Review
  17. Article
  18. 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

8 authors at 3 institutions in 1 country.

Won-Cheoul JangDepartment of Chemistry, School of Advanced Science, Dankook University, Cheonan, South Korea.
Yun-Hyoung Nam
Young-Chang Ahn
Sang-Hyun Lee
Sung-Hoon Park
Jung-Yoon Choe
Shin-Seok Lee
Seong-Kyu Kim
Catholic University of Daegu · KRDankook University · KRChonnam National University · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

IL-17 is a novel cytokine that is characterized by an ability to induce several types of cells to secrete proinflammatory cytokines in various inflammatory diseases. This study analyzed the influence of IL-17F gene polymorphisms on disease susceptibility and clinical features. Ninety-nine Behçet's disease (BD) patients and 114 controls were genotyped to analyze three single nucleotide polymorphisms (SNPs) including A126G, G155A, and A161G of the IL-17F gene using automated sequencing. We compared the frequencies of IL-17F alleles, genotypes, and haplotypes in patients with BD and controls using the chi-square or Fisher's exact test. Significant differences in the frequencies of allele and genotype in A126G SNP of IL-17 gene were found between BD patients and controls (P<0.001 and P<0.001, respectively). None of three IL-17F SNPs were associated with diverse clinical features in BD. The frequency of haplotype AA did not differ between patients with BD and controls (P=0.985). The haplotypes, AG, and GG, have positive and inverse association with BD susceptibility (P<0.001 and P<0.001, respectively). These findings suggest that IL-17 gene SNPs may influence the susceptibility of BD.

Indexed as

Genetic Predisposition to DiseasePolymorphism, Single NucleotideAdultBehcet SyndromeDNA Mutational AnalysisFemaleGene FrequencyGenotypeHumansInterleukin-17KoreaMaleMiddle AgedIL17F protein, humanInterleukin-17

Identifiers

PMID18769923
OpenAlexW2011701106

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.