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Association of juvenile idiopathic arthritis with PTPN22 rs2476601 is specific to females in a Greek population.
Goulielmos, G N; Chiaroni-Clarke, R C; Dimopoulou, D G; Zervou, M I; Trachana, M; Pratsidou-Gertsi, P; Garyfallos, A; Ellis, J A.
Afiliação
  • Goulielmos GN; Laboratory of Molecular Medicine and Human Genetics, Department of Medicine, Medical School of Crete, Heraklion, Greece.
  • Chiaroni-Clarke RC; Genes, Environment and Complex Disease, Murdoch Childrens Research Institute, Parkville, Victoria, 3052, Australia.
  • Dimopoulou DG; Department of Paediatrics, University of Melbourne, Parkville, Victoria, Australia.
  • Zervou MI; Rheumatology Unit, 4th Department of Internal Medicine, Aristotle University of Thessaloniki, Hippocration Hospital, Thessaloniki, Greece.
  • Trachana M; Laboratory of Molecular Medicine and Human Genetics, Department of Medicine, Medical School of Crete, Heraklion, Greece.
  • Pratsidou-Gertsi P; Pediatric Immunology and Rheumatology Referral Center, 1st Department of Pediatrics, Aristotle University, Thessaloniki, Greece.
  • Garyfallos A; Pediatric Immunology and Rheumatology Referral Center, 1st Department of Pediatrics, Aristotle University, Thessaloniki, Greece.
  • Ellis JA; Rheumatology Unit, 4th Department of Internal Medicine, Aristotle University of Thessaloniki, Hippocration Hospital, Thessaloniki, Greece.
Pediatr Rheumatol Online J ; 14(1): 25, 2016 Apr 23.
Article em En | MEDLINE | ID: mdl-27107590
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.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Polimorfismo Genético / Artrite Juvenil / DNA / Predisposição Genética para Doença / Proteína Tirosina Fosfatase não Receptora Tipo 22 Tipo de estudo: Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Female / Humans / Male País/Região como assunto: Europa Idioma: En Ano de publicação: 2016 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Polimorfismo Genético / Artrite Juvenil / DNA / Predisposição Genética para Doença / Proteína Tirosina Fosfatase não Receptora Tipo 22 Tipo de estudo: Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Female / Humans / Male País/Região como assunto: Europa Idioma: En Ano de publicação: 2016 Tipo de documento: Article