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Do all anti-citrullinated protein/peptide antibody tests measure the same? Evaluation of discrepancy between anti-citrullinated protein/peptide antibody tests in patients with and without rheumatoid arthritis
  1. B Vander Cruyssen1,
  2. L Nogueira3,
  3. J Van Praet1,
  4. D Deforce2,
  5. D Elewaut1,
  6. G Serre3,
  7. F De Keyser1
  1. 1
    Department of Rheumatology, Ghent University Hospital, Gent, Belgium
  2. 2
    Laboratory of Pharmaceutical Biotechnology, Ghent University, Ghent, Belgium
  3. 3
    UMR 5165 “Laboratory of Epidermis Differentiation and Rheumatoid Autoimmunity”, CNRS–Toulouse III University, Toulouse, France
  1. Bert Vander Cruyssen, Department of Rheumatology, Ghent University Hospital, B-9000 Gent, Belgium; Bert.VanderCruyssen{at}Ugent.be

Abstract

Background: Different methods exist to demonstrate anti-citrullinated protein/peptide antibodies (ACPA).

Aims: To evaluate discrepancy between four ACPA tests.

Patients and methods: Population 1 consisted of patients with a new diagnostic problem, including 86 patients with rheumatoid arthritis (RA) and 450 patients without RA. Population 2 consisted of 155 patients with RA who had long-standing disease. Population 3 consisted of 188 patients with psoriatic arthritis and in population 4 there were 192 patients with systemic lupus erythematosus. Populations 1 and 2 were tested with the anti-human fibrinogen antibody (AhfibA) test, anti-CCP2 from Eurodiagnostica (CCP2-euro), anti-CCP2 from Pharmacia (CCP2-phar) and anti-CCP3 test by Inova (CCP3). Samples were annotated as discrepant if positive in one and negative in at least one other test. Each discrepant sample was re-analysed in a different run. Populations 3 and 4 were analysed in the CCP2-euro and AhFibA test.

Results: In population 1, ACPA positivity was found in 17 of 450 (3.8%) patients without RA; 14 (82%) of these 17 samples were discrepant. In contrast, 61 of 86 (70.9%) patients with RA were ACPA positive of whom 18 of 61 (29.5%) were discrepant (70.9% vs. 29.5%, p<0.001). The discrepancies between tests could be partly attributed to borderline results, inter-assay discrepancy and inter-test variability. They were more prevalent in patients with systemic lupus erythematosus who were ACPA positive than in those with psoriatic arthritis who were ACPA positive.

Conclusions: Discrepancy between different ACPA tests was observed attributable to the occurrence of borderline results, inter-assay variability and mainly to inter-test variability. The lowest inter-test discrepancy is observed between tests that use the same substrate.

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Footnotes

  • Funding: BVD was supported by a concerted action grant GOA 2001/12051501 of the Ghent University, Belgium. This work was supported by a grant of the “Association pour la Recherche sur la Polyarthrite” and of the “Fondation de l’Avenir pour la Recherche medicale appliquée”

  • Competing interests: None.

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