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Profiling anti-cyclic citrullinated peptide antibodies in patients with juvenile idiopathic arthritis

BACKGROUND: Anti-citrullinated protein/peptide antibodies (ACPA), have high specificity for rheumatoid arthritis (RA). Some children with juvenile idiopathic arthritis (JIA), phenotypically resemble RA and test positive for rheumatoid factor (RF) a characteristic biomarker of RA. We investigated the...

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Autores principales: Tebo, Anne E, Jaskowski, Troy, Davis, K Wayne, Whiting, April, Clifford, Bronte, Zeft, Andrew, McNally, Bernadette, Hill, Harry R, Bohnsack, John, Prahalad, Sampath
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3490766/
https://www.ncbi.nlm.nih.gov/pubmed/22931121
http://dx.doi.org/10.1186/1546-0096-10-29
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author Tebo, Anne E
Jaskowski, Troy
Davis, K Wayne
Whiting, April
Clifford, Bronte
Zeft, Andrew
McNally, Bernadette
Hill, Harry R
Bohnsack, John
Prahalad, Sampath
author_facet Tebo, Anne E
Jaskowski, Troy
Davis, K Wayne
Whiting, April
Clifford, Bronte
Zeft, Andrew
McNally, Bernadette
Hill, Harry R
Bohnsack, John
Prahalad, Sampath
author_sort Tebo, Anne E
collection PubMed
description BACKGROUND: Anti-citrullinated protein/peptide antibodies (ACPA), have high specificity for rheumatoid arthritis (RA). Some children with juvenile idiopathic arthritis (JIA), phenotypically resemble RA and test positive for rheumatoid factor (RF) a characteristic biomarker of RA. We investigated the prevalence of ACPA and its relationship to other serologic markers associated with RA in a well-characterized JIA cohort. METHODS: Cases were 334 children with JIA, 30 of whom had RF + polyarticular JIA. Sera from all cases and 50 healthy pediatric controls were investigated by ELISA at a single time point for anti-cyclic citrullinated peptide (anti-CCP) IgG, RF IgM, IgA and IgG, anti-RA33 IgG, and antinuclear antibodies (ANA). Comparisons between cases and controls were made using Chi-square or Fisher exact tests and T-tests. RESULTS: The prevalence of RF was 8% among controls, and 12% among cases (ns). The prevalence of ACPA was 2% in controls and 14.3% in cases (OR 8.2, p <0.01). Children who were ACPA-positive and RF-negative (n = 23) had a significantly earlier onset-age (4.6 years vs. 12.1 years, p <0.00001) and had fewer HLA-DRB1 shared epitope alleles than those positive for both RF and ACPA (n = 25). Prevalence of anti-RA33 was not different between cases and controls. CONCLUSIONS: ACPAs are detectable in 14% of children with JIA. Children with positive ACPA but negative RF are frequent, and may define a distinct subset of children with JIA. ACPA testing should be included in the classification of JIA.
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spelling pubmed-34907662012-11-07 Profiling anti-cyclic citrullinated peptide antibodies in patients with juvenile idiopathic arthritis Tebo, Anne E Jaskowski, Troy Davis, K Wayne Whiting, April Clifford, Bronte Zeft, Andrew McNally, Bernadette Hill, Harry R Bohnsack, John Prahalad, Sampath Pediatr Rheumatol Online J Research BACKGROUND: Anti-citrullinated protein/peptide antibodies (ACPA), have high specificity for rheumatoid arthritis (RA). Some children with juvenile idiopathic arthritis (JIA), phenotypically resemble RA and test positive for rheumatoid factor (RF) a characteristic biomarker of RA. We investigated the prevalence of ACPA and its relationship to other serologic markers associated with RA in a well-characterized JIA cohort. METHODS: Cases were 334 children with JIA, 30 of whom had RF + polyarticular JIA. Sera from all cases and 50 healthy pediatric controls were investigated by ELISA at a single time point for anti-cyclic citrullinated peptide (anti-CCP) IgG, RF IgM, IgA and IgG, anti-RA33 IgG, and antinuclear antibodies (ANA). Comparisons between cases and controls were made using Chi-square or Fisher exact tests and T-tests. RESULTS: The prevalence of RF was 8% among controls, and 12% among cases (ns). The prevalence of ACPA was 2% in controls and 14.3% in cases (OR 8.2, p <0.01). Children who were ACPA-positive and RF-negative (n = 23) had a significantly earlier onset-age (4.6 years vs. 12.1 years, p <0.00001) and had fewer HLA-DRB1 shared epitope alleles than those positive for both RF and ACPA (n = 25). Prevalence of anti-RA33 was not different between cases and controls. CONCLUSIONS: ACPAs are detectable in 14% of children with JIA. Children with positive ACPA but negative RF are frequent, and may define a distinct subset of children with JIA. ACPA testing should be included in the classification of JIA. BioMed Central 2012-08-29 /pmc/articles/PMC3490766/ /pubmed/22931121 http://dx.doi.org/10.1186/1546-0096-10-29 Text en Copyright ©2012 Tebo et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Tebo, Anne E
Jaskowski, Troy
Davis, K Wayne
Whiting, April
Clifford, Bronte
Zeft, Andrew
McNally, Bernadette
Hill, Harry R
Bohnsack, John
Prahalad, Sampath
Profiling anti-cyclic citrullinated peptide antibodies in patients with juvenile idiopathic arthritis
title Profiling anti-cyclic citrullinated peptide antibodies in patients with juvenile idiopathic arthritis
title_full Profiling anti-cyclic citrullinated peptide antibodies in patients with juvenile idiopathic arthritis
title_fullStr Profiling anti-cyclic citrullinated peptide antibodies in patients with juvenile idiopathic arthritis
title_full_unstemmed Profiling anti-cyclic citrullinated peptide antibodies in patients with juvenile idiopathic arthritis
title_short Profiling anti-cyclic citrullinated peptide antibodies in patients with juvenile idiopathic arthritis
title_sort profiling anti-cyclic citrullinated peptide antibodies in patients with juvenile idiopathic arthritis
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3490766/
https://www.ncbi.nlm.nih.gov/pubmed/22931121
http://dx.doi.org/10.1186/1546-0096-10-29
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