Anticyclic citrullinated peptide antibodies in rheumatoid and nonrheumatoid rheumatic disorders: experience with 1162 patients

Anticyclic citrullinated peptide antibodies (anti-CCP) are considered specific markers of rheumatoid arthritis (RA) and have been included in the revised classification criteria for RA diagnosis. However, these antibodies have also been detected in patients with other types of chronic inflammatory r...

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Published inJournal of rheumatology Vol. 41; no. 12; p. 2395
Main Authors Payet, Judith, Goulvestre, Claire, Bialé, Lisa, Avouac, Jérôme, Wipff, Julien, Job-Deslandre, Chantal, Batteux, Frédéric, Dougados, Maxime, Kahan, André, Allanore, Yannick
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LanguageEnglish
Published Canada 01.12.2014
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Abstract Anticyclic citrullinated peptide antibodies (anti-CCP) are considered specific markers of rheumatoid arthritis (RA) and have been included in the revised classification criteria for RA diagnosis. However, these antibodies have also been detected in patients with other types of chronic inflammatory rheumatism. Our objectives were to identify the prevalence of positive anti-CCP patients in non-RA diseases, to determine the diagnostic value of anti-CCP for the diagnosis of RA, to specify the clinical characteristics of non-RA patients positive for anti-CCP, and to determine the discriminatory value of the levels of anti-CCP in patients among the various diseases. We carried out an observational and descriptive study. All the determinations of anti-CCP requested by the 2 rheumatology departments at Cochin Hospital over a period of 18 months were analyzed. Such determinations were requested for 1162 patients in total. Anti-CCP levels were determined with the Euro Diagnostica ELISA kit, with values ≥ 25 U for this test being considered positive. The diagnosis of rheumatic conditions was the responsibility of the treating physician. Anti-CCP antibodies were detected in 357 (30.7%) of the 1162 patients. The prevalence of anti-CCP was 292/417 (70.0%) in RA, 13/122 (10.6%) in patients with psoriatic arthritis, 13/62 (20.9%) in patients with unclassified rheumatism, 11/33 (33.3%) in patients with primary Sjögren syndrome, 5/30 (16.6%) in patients with systemic lupus erythematosus, 3/28 (10.7%) in patients with mixed connective tissue disorder, 3/36 (8.3%) in patients with systemic sclerosis, 7/44 (15.9%) in patients with juvenile arthritis, and 6/220 (2.7%) in patients with noninflammatory diseases. In the population of patients positive for anti-CCP, mean anti-CCP levels were 869.4 (± 978.4) U/ml, with no significant difference between RA [854.8 (± 959.8) U/ml] and any of the non-RA conditions [922.7 (± 1070.0) U/ml]. Anti-CCP are a hallmark of RA, but may be observed in other inflammatory, systemic, or mechanical diseases. In this large cohort of patients, the presence of second-generation anti-CCP (anti-CCP2) antibodies is useful in diagnosing RA (70% sensitivity, 91.3% specificity), but examining the levels of these antibodies does not appear to offer further discriminatory power among patients who are anti-CCP2-positive.
AbstractList Anticyclic citrullinated peptide antibodies (anti-CCP) are considered specific markers of rheumatoid arthritis (RA) and have been included in the revised classification criteria for RA diagnosis. However, these antibodies have also been detected in patients with other types of chronic inflammatory rheumatism. Our objectives were to identify the prevalence of positive anti-CCP patients in non-RA diseases, to determine the diagnostic value of anti-CCP for the diagnosis of RA, to specify the clinical characteristics of non-RA patients positive for anti-CCP, and to determine the discriminatory value of the levels of anti-CCP in patients among the various diseases. We carried out an observational and descriptive study. All the determinations of anti-CCP requested by the 2 rheumatology departments at Cochin Hospital over a period of 18 months were analyzed. Such determinations were requested for 1162 patients in total. Anti-CCP levels were determined with the Euro Diagnostica ELISA kit, with values ≥ 25 U for this test being considered positive. The diagnosis of rheumatic conditions was the responsibility of the treating physician. Anti-CCP antibodies were detected in 357 (30.7%) of the 1162 patients. The prevalence of anti-CCP was 292/417 (70.0%) in RA, 13/122 (10.6%) in patients with psoriatic arthritis, 13/62 (20.9%) in patients with unclassified rheumatism, 11/33 (33.3%) in patients with primary Sjögren syndrome, 5/30 (16.6%) in patients with systemic lupus erythematosus, 3/28 (10.7%) in patients with mixed connective tissue disorder, 3/36 (8.3%) in patients with systemic sclerosis, 7/44 (15.9%) in patients with juvenile arthritis, and 6/220 (2.7%) in patients with noninflammatory diseases. In the population of patients positive for anti-CCP, mean anti-CCP levels were 869.4 (± 978.4) U/ml, with no significant difference between RA [854.8 (± 959.8) U/ml] and any of the non-RA conditions [922.7 (± 1070.0) U/ml]. Anti-CCP are a hallmark of RA, but may be observed in other inflammatory, systemic, or mechanical diseases. In this large cohort of patients, the presence of second-generation anti-CCP (anti-CCP2) antibodies is useful in diagnosing RA (70% sensitivity, 91.3% specificity), but examining the levels of these antibodies does not appear to offer further discriminatory power among patients who are anti-CCP2-positive.
Author Avouac, Jérôme
Dougados, Maxime
Allanore, Yannick
Kahan, André
Payet, Judith
Batteux, Frédéric
Goulvestre, Claire
Bialé, Lisa
Wipff, Julien
Job-Deslandre, Chantal
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  surname: Payet
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  email: judith.payet@cch.aphp.fr
  organization: From Paris Descartes University, Cochin Hospital, Rheumatology A and Rheumatology B, and Immunology Laboratory, Paris, France.J. Payet, MD, Rheumatology A; J. Avouac, PhD, Rheumatology A; J. Wipff, MD, Rheumatology A; C. Job-Deslandre, MD, Rheumatology A; A. Kahan, PhD, Rheumatology A; Y. Allanore, PhD, Rheumatology A; C. Goulvestre, MD, Immunology Laboratory; F. Batteux, MD, Immunology Laboratory; L. Bialé, MD, Rheumatology B; M. Dougados, MD, Rheumatology B, Paris Descartes University, Cochin Hospital. judith.payet@cch.aphp.fr
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  givenname: Claire
  surname: Goulvestre
  fullname: Goulvestre, Claire
  organization: From Paris Descartes University, Cochin Hospital, Rheumatology A and Rheumatology B, and Immunology Laboratory, Paris, France.J. Payet, MD, Rheumatology A; J. Avouac, PhD, Rheumatology A; J. Wipff, MD, Rheumatology A; C. Job-Deslandre, MD, Rheumatology A; A. Kahan, PhD, Rheumatology A; Y. Allanore, PhD, Rheumatology A; C. Goulvestre, MD, Immunology Laboratory; F. Batteux, MD, Immunology Laboratory; L. Bialé, MD, Rheumatology B; M. Dougados, MD, Rheumatology B, Paris Descartes University, Cochin Hospital
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  surname: Bialé
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  organization: From Paris Descartes University, Cochin Hospital, Rheumatology A and Rheumatology B, and Immunology Laboratory, Paris, France.J. Payet, MD, Rheumatology A; J. Avouac, PhD, Rheumatology A; J. Wipff, MD, Rheumatology A; C. Job-Deslandre, MD, Rheumatology A; A. Kahan, PhD, Rheumatology A; Y. Allanore, PhD, Rheumatology A; C. Goulvestre, MD, Immunology Laboratory; F. Batteux, MD, Immunology Laboratory; L. Bialé, MD, Rheumatology B; M. Dougados, MD, Rheumatology B, Paris Descartes University, Cochin Hospital
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  givenname: Jérôme
  surname: Avouac
  fullname: Avouac, Jérôme
  organization: From Paris Descartes University, Cochin Hospital, Rheumatology A and Rheumatology B, and Immunology Laboratory, Paris, France.J. Payet, MD, Rheumatology A; J. Avouac, PhD, Rheumatology A; J. Wipff, MD, Rheumatology A; C. Job-Deslandre, MD, Rheumatology A; A. Kahan, PhD, Rheumatology A; Y. Allanore, PhD, Rheumatology A; C. Goulvestre, MD, Immunology Laboratory; F. Batteux, MD, Immunology Laboratory; L. Bialé, MD, Rheumatology B; M. Dougados, MD, Rheumatology B, Paris Descartes University, Cochin Hospital
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  surname: Wipff
  fullname: Wipff, Julien
  organization: From Paris Descartes University, Cochin Hospital, Rheumatology A and Rheumatology B, and Immunology Laboratory, Paris, France.J. Payet, MD, Rheumatology A; J. Avouac, PhD, Rheumatology A; J. Wipff, MD, Rheumatology A; C. Job-Deslandre, MD, Rheumatology A; A. Kahan, PhD, Rheumatology A; Y. Allanore, PhD, Rheumatology A; C. Goulvestre, MD, Immunology Laboratory; F. Batteux, MD, Immunology Laboratory; L. Bialé, MD, Rheumatology B; M. Dougados, MD, Rheumatology B, Paris Descartes University, Cochin Hospital
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  givenname: Chantal
  surname: Job-Deslandre
  fullname: Job-Deslandre, Chantal
  organization: From Paris Descartes University, Cochin Hospital, Rheumatology A and Rheumatology B, and Immunology Laboratory, Paris, France.J. Payet, MD, Rheumatology A; J. Avouac, PhD, Rheumatology A; J. Wipff, MD, Rheumatology A; C. Job-Deslandre, MD, Rheumatology A; A. Kahan, PhD, Rheumatology A; Y. Allanore, PhD, Rheumatology A; C. Goulvestre, MD, Immunology Laboratory; F. Batteux, MD, Immunology Laboratory; L. Bialé, MD, Rheumatology B; M. Dougados, MD, Rheumatology B, Paris Descartes University, Cochin Hospital
– sequence: 7
  givenname: Frédéric
  surname: Batteux
  fullname: Batteux, Frédéric
  organization: From Paris Descartes University, Cochin Hospital, Rheumatology A and Rheumatology B, and Immunology Laboratory, Paris, France.J. Payet, MD, Rheumatology A; J. Avouac, PhD, Rheumatology A; J. Wipff, MD, Rheumatology A; C. Job-Deslandre, MD, Rheumatology A; A. Kahan, PhD, Rheumatology A; Y. Allanore, PhD, Rheumatology A; C. Goulvestre, MD, Immunology Laboratory; F. Batteux, MD, Immunology Laboratory; L. Bialé, MD, Rheumatology B; M. Dougados, MD, Rheumatology B, Paris Descartes University, Cochin Hospital
– sequence: 8
  givenname: Maxime
  surname: Dougados
  fullname: Dougados, Maxime
  organization: From Paris Descartes University, Cochin Hospital, Rheumatology A and Rheumatology B, and Immunology Laboratory, Paris, France.J. Payet, MD, Rheumatology A; J. Avouac, PhD, Rheumatology A; J. Wipff, MD, Rheumatology A; C. Job-Deslandre, MD, Rheumatology A; A. Kahan, PhD, Rheumatology A; Y. Allanore, PhD, Rheumatology A; C. Goulvestre, MD, Immunology Laboratory; F. Batteux, MD, Immunology Laboratory; L. Bialé, MD, Rheumatology B; M. Dougados, MD, Rheumatology B, Paris Descartes University, Cochin Hospital
– sequence: 9
  givenname: André
  surname: Kahan
  fullname: Kahan, André
  organization: From Paris Descartes University, Cochin Hospital, Rheumatology A and Rheumatology B, and Immunology Laboratory, Paris, France.J. Payet, MD, Rheumatology A; J. Avouac, PhD, Rheumatology A; J. Wipff, MD, Rheumatology A; C. Job-Deslandre, MD, Rheumatology A; A. Kahan, PhD, Rheumatology A; Y. Allanore, PhD, Rheumatology A; C. Goulvestre, MD, Immunology Laboratory; F. Batteux, MD, Immunology Laboratory; L. Bialé, MD, Rheumatology B; M. Dougados, MD, Rheumatology B, Paris Descartes University, Cochin Hospital
– sequence: 10
  givenname: Yannick
  surname: Allanore
  fullname: Allanore, Yannick
  organization: From Paris Descartes University, Cochin Hospital, Rheumatology A and Rheumatology B, and Immunology Laboratory, Paris, France.J. Payet, MD, Rheumatology A; J. Avouac, PhD, Rheumatology A; J. Wipff, MD, Rheumatology A; C. Job-Deslandre, MD, Rheumatology A; A. Kahan, PhD, Rheumatology A; Y. Allanore, PhD, Rheumatology A; C. Goulvestre, MD, Immunology Laboratory; F. Batteux, MD, Immunology Laboratory; L. Bialé, MD, Rheumatology B; M. Dougados, MD, Rheumatology B, Paris Descartes University, Cochin Hospital
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DIAGNOSIS
ANTICYCLIC CITRULLINATED PEPTIDE ANTIBODIES
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References 25729050 - J Rheumatol. 2015 Mar;42(3):558
26034235 - J Rheumatol. 2015 Jun;42(6):1063-4
25452177 - J Rheumatol. 2014 Dec;41(12):2340-2
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Snippet Anticyclic citrullinated peptide antibodies (anti-CCP) are considered specific markers of rheumatoid arthritis (RA) and have been included in the revised...
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SubjectTerms Adult
Aged
Antibodies, Anti-Idiotypic - blood
Arthritis, Juvenile - blood
Arthritis, Juvenile - diagnosis
Arthritis, Juvenile - immunology
Arthritis, Psoriatic - blood
Arthritis, Psoriatic - diagnosis
Arthritis, Psoriatic - immunology
Arthritis, Rheumatoid - blood
Arthritis, Rheumatoid - diagnosis
Arthritis, Rheumatoid - immunology
Biomarkers - blood
Diagnosis, Differential
Female
Humans
Lupus Erythematosus, Systemic - blood
Lupus Erythematosus, Systemic - diagnosis
Lupus Erythematosus, Systemic - immunology
Male
Middle Aged
Mixed Connective Tissue Disease - blood
Mixed Connective Tissue Disease - diagnosis
Mixed Connective Tissue Disease - immunology
Peptides, Cyclic - immunology
Retrospective Studies
Rheumatic Diseases - blood
Rheumatic Diseases - diagnosis
Rheumatic Diseases - immunology
Scleroderma, Systemic - blood
Scleroderma, Systemic - diagnosis
Scleroderma, Systemic - immunology
Sensitivity and Specificity
Sjogren's Syndrome - blood
Sjogren's Syndrome - diagnosis
Sjogren's Syndrome - immunology
Title Anticyclic citrullinated peptide antibodies in rheumatoid and nonrheumatoid rheumatic disorders: experience with 1162 patients
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