Evidence map›Paper›PMID 26610302›Full record

ArticleGenes and immunity

The genetic associations of acute anterior uveitis and their overlap with the genetics of ankylosing spondylitis.

P C Robinson, P J Leo, J J Pointon, J Harris, K Cremin, L A Bradbury, Wellcome Trust Case Control Consortium, Australasian Osteoporosis Genetics Consortium (AOGC), S Stebbings, A A Harrison and 5 more

Abstract read
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In one paragraph

Article in Genes and immunity. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed, 3 pooled it
3.8field-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

19 citing papers in PubMed, 3 syntheses or guidelines pooled it, 43 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Pooled it
  4. Exploring the Involvement ofLife (Basel, Switzerland) · 2026
    Review
  5. Article
  6. Review
  7. Review
  8. Article
  9. Progress in the genetics of uveitis.Genes and immunity · 2022
    Review
  10. Article
  11. Article
  12. Genetics and the axial spondyloarthritis spectrum.Rheumatology (Oxford, England) · 2020
    Review
  13. Article
  14. Relationship of CARD8 Gene Polymorphisms with Susceptibility to Ankylosing Spondylitis: A Case-Control Study.Medical science monitor : international medical journal of experimental and clinical research · 2020
    Article
  15. Review
  16. Article
  17. Review
  18. Article
  19. Observational
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

15 authors at 7 institutions in 3 countries.

P C RobinsonCentre for Neurogenetics and Statistical Genomics, Queensland Brain Institute, University of Queensland, Brisbane, QLD, Australia.
P J LeoUniversity of Queensland Diamantina Institute, Translational Research Institute, Princess Alexandra Hospital, Brisbane, QLD, Australia.
J J PointonNational Institute for Health Research (NIHR) Oxford Musculoskeletal Biomedical Research Unit and Comprehensive Biomedical Research Centre, Nuffield Orthopaedic Centre, Headington, Oxford, UK.
J HarrisUniversity of Queensland Diamantina Institute, Translational Research Institute, Princess Alexandra Hospital, Brisbane, QLD, Australia.
K CreminUniversity of Queensland Diamantina Institute, Translational Research Institute, Princess Alexandra Hospital, Brisbane, QLD, Australia.
L A BradburyUniversity of Queensland Diamantina Institute, Translational Research Institute, Princess Alexandra Hospital, Brisbane, QLD, Australia.
Wellcome Trust Case Control Consortium
Australasian Osteoporosis Genetics Consortium (AOGC)
S StebbingsDepartment of Medicine, University of Otago, Dunedin, New Zealand.
A A HarrisonDepartment of Medicine, University of Otago, Wellington, New Zealand.
D M EvansUniversity of Queensland Diamantina Institute, Translational Research Institute, Princess Alexandra Hospital, Brisbane, QLD, Australia.
E L DuncanUniversity of Queensland Diamantina Institute, Translational Research Institute, Princess Alexandra Hospital, Brisbane, QLD, Australia.
B P WordsworthNational Institute for Health Research (NIHR) Oxford Musculoskeletal Biomedical Research Unit and Comprehensive Biomedical Research Centre, Nuffield Orthopaedic Centre, Headington, Oxford, UK.
M A BrownUniversity of Queensland Diamantina Institute, Translational Research Institute, Princess Alexandra Hospital, Brisbane, QLD, Australia.
Australasian Osteoporosis Genetics Consortium AOGC
Princess Alexandra Hospital · AUThe University of Queensland · AUTranslational Research Institute · AUUniversity of Otago · NZNational Institute for Health Research · GBNuffield Orthopaedic Centre · GBRoyal Brisbane and Women's Hospital · AU

Funding

Arthritis Research UK 18797Arthritis Research UK 19536Medical Research Council G0400491Medical Research Council MC_U147585819Medical Research Council MC_U147585824Medical Research Council MC_U147585827Medical Research Council MC_UP_A620_1014Medical Research Council MC_UU_12011/1Medical Research Council MC_UU_12013/4Versus Arthritis 19583
6 · The paper itself

Abstract

Acute anterior uveitis (AAU) involves inflammation of the iris and ciliary body of the eye. It occurs both in isolation and as a complication of ankylosing spondylitis (AS). It is strongly associated with HLA-B*27, but previous studies have suggested that further genetic factors may confer additional risk. We sought to investigate this using the Illumina Exomechip microarray, to compare 1504 cases with AS and AAU, 1805 with AS but no AAU and 21 133 healthy controls. We also used a heterogeneity test to test the differences in effect size between AS with AAU and AS without AAU. In the analysis comparing AS+AAU+ cases versus controls, HLA-B*27 and HLA-A*02:01 were significantly associated with the presence of AAU (P<10(-300) and P=6 × 10(-8), respectively). Secondary independent association with PSORS1C3 (P=4.7 × 10(-5)) and TAP2 (P=1.1 × 10(-5)) were observed in the major histocompatibility complex. There was a new suggestive association with a low-frequency variant at zinc-finger protein 154 in the AS without AAU versus control analysis (zinc-finger protein 154 (ZNF154), P=2.2 × 10(-6)). Heterogeneity testing showed that rs30187 in ERAP1 has a larger effect on AAU compared with that in AS alone. These findings also suggest that variants in ERAP1 have a differential impact on the risk of AAU when compared with AS, and hence the genetic risk for AAU differs from AS.

Indexed as

Polymorphism, Single NucleotideCase-Control StudiesGenetic HeterogeneityHLA-B27 AntigenHumansSpondylitis, AnkylosingUveitis, AnteriorHLA-B27 Antigen

Identifiers

PMID26610302
OpenAlexW2279973807

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.