Article Text

Download PDFPDF
Associations between the PTPN22 1858C→T polymorphism and radiographic joint destruction in patients with rheumatoid arthritis: results from a 10-year longitudinal study
  1. Benedicte A Lie1,
  2. Marte K Viken1,
  3. Sigrid Ødegård2,
  4. Désirée van der Heijde3,
  5. Robert Landewé3,
  6. Till Uhlig2,
  7. Tore K Kvien2
  1. 1
    Institute of Immunology, Rikshospitalet-Radiumhospitalet Medical Center, Oslo, Norway
  2. 2
    Department of Rheumatology, Diakonhjemmet Hospital, Oslo, Norway
  3. 3
    Department of Rheumatology, University Hospital Maastricht, Maastricht, The Netherlands
  1. Benedicte A Lie, Institute of Immunology, Rikshospitalet-Radiumhospitalet Medical Center, N-0027 Oslo, Norway; b.a.lie{at}


Objective: To investigate whether the PTPN22 1858T risk variant is associated with the rate of radiographic progression in rheumatoid arthritis (RA).

Methods: A longitudinally followed cohort of 238 Norwegian patients with RA (the EURIDISS cohort) was genotyped for the PTPN22 1858C→T polymorphism. Radiographic damage was assessed by hand radiographs at baseline and after 1, 2, 5 and 10 years, and the radiographs were scored with the Sharp method modified by van der Heijde (Sharp–van der Heijde score) by a single experienced reader. Baseline serum levels of rheumatoid factor and anti-cyclic citrullinated peptide autoantibodies were also examined.

Results: The reported association between RA susceptibility and carriage of the T allele (34.4% in patients vs 21.4% in controls; odds ratio 1.92, 95% confidence interval 1.36 to 2.71, p = 0.0002) was confirmed. An association between annual progression rate of Sharp–van der Heijde score and T-allele carriers (p = 0.01),was also found, which was also present when only patients positive for the shared epitope were analysed (p = 0.03). This association was also maintained in multivariate analyses adjusting for shared epitope and demographic variables.

Conclusions: An association between the PTPN22 risk variant and increased progression rate for structural damage was found. The results indicate that the PTPN22 gene may not only be associated with disease susceptibility, but also with disease progression.

  • rheumatoid arthritis
  • PTPN22
  • longitudinal study
  • radiographic damage
  • genetic predisposition

Statistics from


  • This study was financed by Rikshospitalet, the Research Council of Norway and Southern Norway Regional Health Authority.

  • Abbreviations:
    American College of Rheumatology
    analysis of variance
    cyclic citrullinated peptide
    European Research on Incapacitating Disease and Social Support
    erythrocyte sedimentation rate
    Health Assessment Questionnaire
    joint-space narrowing
    protein tyrosine phosphatase N22
    rheumatoid arthritis
    rheumatoid factor
    shared epitope

Request Permissions

If you wish to reuse any or all of this article please use the link below which will take you to the Copyright Clearance Center’s RightsLink service. You will be able to get a quick price and instant permission to reuse the content in many different ways.