Evidence map›Paper›PMID 20722033›Full record

ArticleArthritis and rheumatism2010

The susceptibility loci juvenile idiopathic arthritis shares with other autoimmune diseases extend to PTPN2, COG6, and ANGPT1.

Susan D Thompson, Marc Sudman, Paula S Ramos, Miranda C Marion, Mary Ryan, Monica Tsoras, Tracey Weiler, Michael Wagner, Mehdi Keddache, J Peter Haas and 11 more

Open access · greenAbstract read
In one paragraph

Article in Arthritis and rheumatism, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 65 papers, 7 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
65citing papers in PubMed, 7 pooled it
4.2field-weighted citation impact, top 5% 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

65 citing papers in PubMed, 7 syntheses or guidelines pooled it, 128 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
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  5. Pooled it
  6. The association between the functional PTPN22 1858 C/T and MIF -173 C/G polymorphisms and juvenile idiopathic arthritis: a meta-analysis.Inflammation research : official journal of the European Histamine Research Society ... [et al.] · 2012
    Pooled it
  7. Pooled it
  8. Trial
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  10. Review
  11. Article
  12. Genome-Wide Association Study of Reproductive Traits in Large White Pigs.Animals : an open access journal from MDPI · 2024
    Article
  13. Article
  14. Review
  15. Genetic association between theExperimental and therapeutic medicine · 2022
    Article
  16. Article
  17. Article
  18. Article
  19. Spondyloarthritides: Theories and beyond.Frontiers in pediatrics · 2022
    Review
  20. Article

5 more citing papers are in PubMed but not listed here.

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

21 authors at 1 institution in 1 country.

Susan D ThompsonCincinnati Children's Hospital Medical Center, Cincinnati, Ohio 45229, USA. susan.thompson@cchmc.org
Marc Sudman
Paula S Ramos
Miranda C Marion
Mary Ryan
Monica Tsoras
Tracey Weiler
Michael Wagner
Mehdi Keddache
J Peter Haas
Cornelia Mueller
Sampath Prahalad
John Bohnsack
Carol A Wise
Marilynn Punaro
Dongping Zhang
Carlos D Rosé
Mary E Comeau
Jasmin Divers
David N Glass
Carl D Langefeld
Cincinnati Children's Hospital Medical Center · US

Funding

ROLE OF ANGPTL4, AN ANGIOGENIC MEDIATOR, IN ARTHRITISP30AR047363 · NIAMS · CINCINNATI CHILDRENS HOSP MED CTR · PI WAGNER, MICHAEL · 2001 to 2015
$9.2M
HLA/KIR Region Genetics in Pediatric ArthritisU01AI067150 · NIAID · CINCINNATI CHILDRENS HOSP MED CTR · PI GLASS, DAVID N. · 2005 to 2010
$2.4M
Defining the complex genetics of JIARC1AR058587 · NIAMS · CINCINNATI CHILDRENS HOSP MED CTR · PI THOMPSON, SUSAN D · 2009 to 2010
$1.0M
Genetic variation in T-cell regulatory molecules and JRAK23AR050177 · NIAMS · UNIVERSITY OF UTAH · PI PRAHALAD, SAMPATH · 2004 to 2008
$674k
Genetics of Juvenile Idiopathic Arthritis and SubtypesR01AR057106 · NIAMS · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI LANGEFELD, CARL D, THOMPSON, SUSAN D · 2009 to 2010
$592k
NHLBI NIH HHS N01 AR042272NIAID NIH HHS U01 AI067150NIAID NIH HHS U01-AI-067150NIAMS NIH HHS K23 AR050177NIAMS NIH HHS K23-AR-50177NIAMS NIH HHS N01-AR-42272NIAMS NIH HHS P30 AR047363NIAMS NIH HHS P30-AR-473639NIAMS NIH HHS R01 AR057106NIAMS NIH HHS R01-AR-057106NIAMS NIH HHS RC1 AR058587NIAMS NIH HHS RC1-AR-058587Wellcome Trust
6 · The paper itself

Abstract

objectiveTo test for associations between non-major histocompatibility complex susceptibility loci previously reported in autoimmune diseases and juvenile idiopathic arthritis (JIA).

methodsPublished autoimmune disease genome-wide association studies were reviewed, and 519 single-nucleotide polymorphisms (SNPs) were selected for association testing. The initial cohort included 809 JIA cases and 3,535 controls of non-Hispanic, European ancestry. Of the SNPs, 257 were successfully genotyped, while 168 were imputed with quality. Based on findings in the initial cohort, replication was sought for 21 SNPs in a second cohort of 1,015 JIA cases and 1,569 controls collected in the US and Germany. For the initial cohort, tests for association were adjusted for potential confounding effects of population structure by including principal components derived from a genome-wide association study as covariates in logistic regression models. Odds ratios (ORs) and 95% confidence intervals were calculated.

resultsTesting for association of previously reported autoimmune disease genetic associations in the initial cohort suggested associations with JIA in 13 distinct loci. Of these, 7 were validated in the replication cohort. Meta-analysis results for the replicating loci included PTPN22 (rs6679677 [OR 1.58, P = 1.98 × 10(-12) ], rs2476601 [OR 1.64, P = 1.90 × 10(-13) ], and rs2488457 [OR 1.32, P = 6.74 × 10(-8) ]), PTPN2 (rs1893217 [OR = 1.33, P = 1.60 × 10(-9) ] and rs7234029 [OR 1.35, P = 1.86 × 10(-10) ]), ADAD1-IL2-IL21 (rs17388568 [OR 1.24, P = 1.13 × 10(-6) ] and rs13143866 [OR 0.83, P = 1.95 × 10(-4) ]), STAT4 (rs3821236 [OR = 1.27, P = 2.36 × 10(-6) ] and rs7574865 [OR = 1.31, P = 2.21 × 10(-6) ]), C12orf30 (rs17696736 [OR = 1.19, P = 2.59 × 10(-5) ]), COG6 (rs7993214 [OR = 0.76, P = 1.10 × 10(-5) ]), and ANGPT1 (rs1010824 [OR = 0.79, P = 2.91 × 10(-4) ]). These polymorphisms have been reported in diseases such as rheumatoid arthritis, type 1 diabetes mellitus, Crohn's disease, and multiple sclerosis.

conclusionGeneral susceptibility loci for autoimmunity are shared across diseases, including JIA, suggesting the potential for common therapeutic targets and mechanisms.

Indexed as

Adaptor Proteins, Vesicular TransportAllelesAngiopoietin-1Arthritis, JuvenileChildChild, PreschoolFemaleGene FrequencyGenetic Association StudiesGenetic Predisposition to DiseaseGenotypeHumansMaleOdds RatioPolymorphism, Single NucleotideProtein Tyrosine Phosphatase, Non-Receptor Type 2Adaptor Proteins, Vesicular TransportAngiopoietin-1ANGPT1 protein, humanCOG6 protein, humanProtein Tyrosine Phosphatase, Non-Receptor Type 2PTPN2 protein, human

Identifiers

PMID20722033
PMCPMC2970764
OpenAlexW2079511996

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.