Your browser doesn't support javascript.
loading
No association of IL-12p40 pro1.1 polymorphism with juvenile idiopathic arthritis.
Eberhardt, Christiane S; Haas, Johannes-Peter; Girschick, Hermann; Schwarz, Tobias; Morbach, Henner; Rösen-Wolff, Angela; Foell, Dirk; Dannecker, Guenther; Schepp, Carsten; Ganser, Gerd; Honke, Nora; Eggermann, Thomas; Müller-Berghaus, Jan; Wagner, Norbert; Ohl, Kim; Tenbrock, Klaus.
Afiliação
  • Eberhardt CS; Département de l'enfant et de l'adolescent, Hôpitaux Universitaires de Genève, Genève, Switzerland. christiane.eberhardt@gmail.com.
  • Haas JP; Deutsches Zentrum für Kinder- und Jugendrheumatologie, Garmisch-Partenkirchen, Germany. Haas.Johannes-Peter@rheuma-kinderklinik.de.
  • Girschick H; Klinik für Kinder- und Jugendmedizin, Vivantes Klinikum im Friedrichshain, Berlin, Germany. Hermann.Girschick@vivantes.de.
  • Schwarz T; Kinderklinik der Bayerischen Julius-Maximilians-Universität, Universitätsklinikum, Würzburg, Germany. Schwarz@st-josef-stift.de.
  • Morbach H; Kinderklinik der Bayerischen Julius-Maximilians-Universität, Universitätsklinikum, Würzburg, Germany. Morbach_H@kinderklinik.uni-wuerzburg.de.
  • Rösen-Wolff A; Klinik für Kinder- und Jugendmedizin, Universitätsklinikum Carl Gustav Carus, Dresden, Germany. Angela.Roesen-Wolff@uniklinikum-dresden.de.
  • Foell D; Institut für Immunologie, Universität Münster, Münster, Germany. dfoell@uni-muenster.de.
  • Dannecker G; Pädiatrie 5, Olgahospital Stuttgart, Stuttgart, Germany. guenther.dannecker@gmx.de.
  • Schepp C; Klinik für Anästhesiologie, Klinikum der Universität Regensburg, Regensburg, Germany. Carsten.Schepp@gmx.de.
  • Ganser G; Klinik für Kinder-und Jugendrheumatologie, St Josef Stift Sendenhorst, Sendenhorst, Germany. ganser@st-josef-stift.de.
  • Honke N; Department of Pediatrics, Division of Pediatric Pneumology, Allergology and Immunology, RWTH Aachen, University, Pauwelsstr 30, D-52074, Aachen, Germany. nhonke@ukaachen.de.
  • Eggermann T; Institut für Humangenetik, Heidelberg, Germany. theggermann@ukaachen.de.
  • Müller-Berghaus J; Paul-Ehrlich Institut, Langen, Germany. jan.muellerberghaus@gmail.com.
  • Wagner N; Department of Pediatrics, Division of Pediatric Pneumology, Allergology and Immunology, RWTH Aachen, University, Pauwelsstr 30, D-52074, Aachen, Germany. nwagner@ukaachen.de.
  • Ohl K; Department of Pediatrics, Division of Pediatric Pneumology, Allergology and Immunology, RWTH Aachen, University, Pauwelsstr 30, D-52074, Aachen, Germany. kohl@ukaachen.de.
  • Tenbrock K; Department of Pediatrics, Division of Pediatric Pneumology, Allergology and Immunology, RWTH Aachen, University, Pauwelsstr 30, D-52074, Aachen, Germany. ktenbrock@ukaachen.de.
Pediatr Rheumatol Online J ; 13: 61, 2015 Dec 15.
Article em En | MEDLINE | ID: mdl-26667304
ABSTRACT

BACKGROUND:

IL-12p40 plays an important role in the activation of the T-cell lines like Th17 and Th1-cells. Theses cells are crucial in the pathogenesis of juvenile idiopathic arthritis. A polymorphism in its promoter region and the genotype IL12p40 pro1.1 leads to a higher production of IL-12p40. We studied whether there is a difference in the distribution of the genotype in patients with JIA and the healthy population.

METHODS:

In 883 patients and 321 healthy controls the IL-12p40 promoter genotype was identified by ARMS-PCR.

RESULTS:

There is no association of IL-12p40 pro polymorphism neither in patients with JIA compared to controls nor in subtypes of JIA compared to oligoarthritis. We found a non-significant tendency of a higher prevalence of the genotype pro1.1 in systemic arthritis (32.4%) and in rheumatoid factor negative polyarthritis (30.5%) and a lower pro1.1 genotype in persistent oligoarthritis (20.7%) and in enthesitis-related arthritis (17%). Likelihood of the occurrence of genotype IL12-p40 pro1.1 in patients with systemic arthritis (OR 1.722, CI 95% 1.344-2.615, p 0.0129) and RF-negative polyarthritis (OR 1.576, CI 95% 1.046-2.376, p 0.0367) compared to persistent oligoarthritis was significantly higher. This was also true for comparison of their homozygous genotypes IL-12p40 pro 1.1 and 2.2 in systemic arthritis (OR 1.779, CI 95 % 1.045-3.029, p 0.0338). However, in Bonferroni correction for multiple hypothesis this was not significant.

CONCLUSION:

A tendency of a higher prevalence of the genotype IL-12p40 pro1.1 in systemic arthritis and in rheumatoid factor negative polyarthritis was observed but not significant. Further investigations should be done to clarify the role IL-12p40 in the different subtypes of JIA.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Polimorfismo Genético / Artrite Juvenil / Subunidade p40 da Interleucina-12 Idioma: En Ano de publicação: 2015 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Polimorfismo Genético / Artrite Juvenil / Subunidade p40 da Interleucina-12 Idioma: En Ano de publicação: 2015 Tipo de documento: Article