Evidence map›Paper›PMID 22130325›Full record

ArticleGenes and immunity2012

IL-23R rs11209026 polymorphism modulates IL-17A expression in patients with rheumatoid arthritis.

J Hazlett, L K Stamp, T Merriman, J Highton, P A Hessian

Open access · bronzeAbstract read
PubMed Publisher
In one paragraph

Article in Genes and immunity, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers, 4 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed, 4 pooled it
1.9field-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

20 citing papers in PubMed, 4 syntheses or guidelines pooled it, 47 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Pooled it
  4. Pooled it
  5. Review
  6. IL-23R gene polymorphisms in rheumatoid arthritis.Rheumatology international · 2022
    Article
  7. Article
  8. Article
  9. Kynurenic acid downregulates IL-17/1L-23 axis in vitro.Molecular and cellular biochemistry · 2017
    Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Review
  15. Unexpected targets and triggers of autoimmunity.Journal of clinical immunology · 2014
    Review
  16. Article
  17. Role of non-HLA gene polymorphisms in graft-versus-host disease.International journal of hematology · 2013
    Review
  18. Review
  19. Article
  20. 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

5 authors at 1 institution in 1 country.

J HazlettLeukocyte Inflammation Research Laboratory, Department of Physiology, University of Otago, Dunedin, New Zealand.
L K Stamp
T Merriman
J Highton
P A Hessian
University of Otago · NZ

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The interleukin (IL)-17/IL-23 axis is an important pro-inflammatory pathway in rheumatoid arthritis (RA). IL-23 maintains CD4(+) T-helper 17 (Th(17)) cells, whereas IL-12 negates IL-17A production by promoting Th(1)-cell differentiation. We sought evidence for any effect of polymorphisms within the interleukin-23 receptor (IL-23R), IL-12 or IL-21 genes on serum cytokine concentrations in 81 patients with RA. Serum cytokines were measured using bead-based multiplex assays. Targeted cytokines were detected in up to 66% of samples. A subgroup of 48 patients had detectable serum IL-17A. Within this subgroup, patients, homozygous for the IL-23R rs11209026 major allele had significantly higher serum IL-17A concentrations compared with patients with the minor allele (394.51 ± 529.72 pg ml(-1) vs 176.11 ± 277.32 pg ml(-1); P = 0.017). There was no significant difference in any of the cytokine concentrations examined in patients positive for the minor allele vs homozygosity for the major allele of IL-12B rs3213337, IL-12Bpro rs17860508 and IL-21 rs6822844. Our results suggest the IL-23R Arg381Gln substitution may influence serum IL-17A concentrations. In patients with the 381Gln allele higher IL-23 concentrations may be needed to produce similar IL-17A concentrations to those in patients with the 381Arg allele. This suggests altered IL-23R function in patients with the minor allele and warrants further functional studies.

Indexed as

Polymorphism, Single NucleotideAdultAgedAged, 80 and overArthritis, RheumatoidC-Reactive ProteinFemaleGenotypeHumansInterleukin-12Interleukin-17Interleukin-21InterleukinsMaleMiddle AgedReceptors, InterleukinC-Reactive ProteinIL23R protein, humanInterleukin-12Interleukin-17Interleukin-21InterleukinsReceptors, Interleukin

Identifiers

PMID22130325
OpenAlexW2028939278

What OpenQuestion holds

Textmetadata
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.