Arthritis development in patients with arthralgia is strongly associated with anti-citrullinated protein antibody status: a prospective cohort study

Ann Rheum Dis. 2010 Mar;69(3):490-4. doi: 10.1136/ard.2008.105759. Epub 2009 Apr 9.

Abstract

Background: Anti-citrullinated protein antibodies (ACPA) are associated with increased risk for rheumatoid arthritis.

Objective: To investigate the effect of the presence and levels of ACPA on arthritis development in patients with arthralgia.

Methods: Patients with arthralgia positive for ACPA or IgM rheumatoid factor (IgM-RF) were tested for the shared epitope (SE) and were prospectively followed up for at least 12 months. Absence of clinical arthritis at inclusion and arthritis development during follow-up were independently confirmed by two investigators. Cox regression hazard analyses were used to calculate hazard ratios (HRs) for arthritis development.

Results: 147 patients with arthralgia were included (50 ACPA positive, 52 IgM-RF positive and 45 positive for both antibodies). After a median follow-up of 28 months (interquartile range (IQR) 19-39), 29 patients developed arthritis in a median of 4 (IQR 3-6) joints and 26 (90%) of these were ACPA positive. The presence of ACPA (HR = 6.0; 95% confidence interval (95% CI) 1.8 to 19.8; p = 0.004), but not of IgM-RF (HR = 1.4, 95% CI 0.6 to 3.1) nor the SE (HR = 1.5, 95% CI 0.7 to 3.0), was associated with arthritis development. Within the group of ACPA-positive patients, the risk for arthritis was enhanced by the presence of IgM-RF (HR = 3.0; 95% CI 1.4 to 6.9; p = 0.01) and high ACPA levels (HR = 1.7; 95% CI 1.1 to 2.5; p = 0.008), but not the SE (HR = 1.0; 95% CI 0.5 to 2.1; p = 1.0).

Conclusion: In patients with arthralgia the presence of ACPA (but not of IgM-RF or SE) predicts arthritis development. The risk in ACPA-positive patients may be further increased by the concomitant presence of IgM-RF or high levels of ACPA.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Arthralgia / immunology*
  • Arthralgia / metabolism
  • Arthritis, Rheumatoid / immunology*
  • Arthritis, Rheumatoid / metabolism
  • Epidemiologic Methods
  • Epitopes / immunology
  • Epitopes / metabolism
  • Female
  • Humans
  • Immunoglobulin M / immunology*
  • Immunoglobulin M / metabolism
  • Male
  • Middle Aged
  • Peptides, Cyclic / immunology*
  • Peptides, Cyclic / metabolism
  • Rheumatoid Factor / immunology*
  • Rheumatoid Factor / metabolism

Substances

  • Epitopes
  • Immunoglobulin M
  • Peptides, Cyclic
  • cyclic citrullinated peptide
  • Rheumatoid Factor