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Association of juvenile idiopathic arthritis with PTPN22 rs2476601 is specific to females in a Greek population.

TitleAssociation of juvenile idiopathic arthritis with PTPN22 rs2476601 is specific to females in a Greek population.
Publication TypeJournal Article
Year of Publication2016
AuthorsGoulielmos, G. N., Chiaroni-Clarke R. C., Dimopoulou D. G., Zervou M. I., Trachana M., Pratsidou-Gertsi P., Garyfallos A., & Ellis J. A.
JournalPediatr Rheumatol Online J
Volume14
Issue1
Pagination25
Date Published2016 Apr 23
ISSN1546-0096
KeywordsAlleles, Arthritis, Juvenile, DNA, Female, Gene Frequency, Genetic Predisposition to Disease, Genotype, Greece, Humans, Incidence, Male, Polymorphism, Genetic, Protein Tyrosine Phosphatase, Non-Receptor Type 22, Retrospective Studies, Risk Factors, Sex Factors
Abstract

BACKGROUND: Juvenile idiopathic arthritis (JIA) is an autoimmune disease characterized by persistent chronic arthritis. Disease risk is believed to be influenced by both genetic and environmental factors. It is well established that the PTPN22 single nucleotide polymorphism (SNP) rs2476601 is associated with JIA susceptibility. It was recently reported in an Australian study that this association is restricted to females and is not observed in males. A significant source of inconsistency amongst the literature on autoimmune disease susceptibility genes stems from an inability to replicate genetic findings across different racial or ethnic groups. We therefore attempted to generate further evidence of the female-specific association of rs2476601 in a homogeneous Greek population.FINDINGS: We genotyped rs2476601 in 128 Caucasian JIA patients (70.3 % female) and 221 healthy controls (28.1 % female) from Northern Greece. Overall, PTPN22 was associated with increased risk of JIA in this Greek sample (OR = 2.3, 95 % CI 1.1 - 5.1, p = 0.038). Sex-stratified analyses showed that, once again, the risk association was restricted to females (Female: OR = 19.9, 95 % CI 1.2 - 342, p = 0.0016; Male: OR = 1.1, 95 % CI 0.3 - 3.1, p = 0.94) supporting the prior findings.CONCLUSIONS: Our data demonstrates that this sex-specific pattern of association is broadly applicable to different populations, and provides further impetus to undertake mechanistic studies to understand the impact of sex on PTPN22 in JIA.

DOI10.1186/s12969-016-0087-3
Alternate JournalPediatr Rheumatol Online J
PubMed ID27107590
PubMed Central IDPMC4842296

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