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Circulating Cartilage Oligomeric Matrix Protein in Juvenile Idiopathic Arthritis

Overview
Publisher Informa Healthcare
Specialty Rheumatology
Date 2016 Jul 8
PMID 27385219
Citations 5
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Abstract

Objectives: Raised serum cartilage oligomeric matrix protein (sCOMP) has been reported to predict erosive disease in early rheumatoid arthritis (RA). In juvenile idiopathic arthritis (JIA), subnormal sCOMP levels have been associated with ongoing inflammation and growth retardation. In this study we aimed to assess sCOMP, C-reactive protein (CRP), and insulin-like growth factor (IGF)-1 in children/adolescents with JIA and in referents.

Method: We enrolled 52 JIA patients at planned outpatient visits and 54 inpatients with ongoing infection ('infection referents'). A total of 120 referents testing negative for immunoglobulin (Ig)E-mediated allergy ('IgE referents') served as controls. All serum samples were analysed for COMP, IGF-1, and CRP.

Results: The average sCOMP level was highest among the IgE referents and lowest among the infection referents. In the JIA patients, the level of sCOMP was not associated with the level of CRP or with clinical signs of disease activity.

Conclusions: The results of this study do not support routine clinical analysis of sCOMP levels in patients with JIA.

Citing Articles

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Serum levels of soluble urokinase plasminogen activator receptor in juvenile idiopathic arthritis: a single-center Swedish case-control study.

Lewander P, Wirestam L, Dahle C, Wettero J, Sjowall C Pediatr Rheumatol Online J. 2023; 21(1):49.

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GAAGs, COMP, and YKL-40 as Potential Markers of Cartilage Turnover in Blood of Children with Juvenile Idiopathic Arthritis Treated with Etanercept-Relationship with ADAMTS4, ADAMTS5, and PDGF-BB.

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Concerted Actions by PIICP, CTXII, and TNF-α in Patients with Juvenile Idiopathic Arthritis.

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Association of Circulating COMP and YKL-40 as Markers of Metabolic Changes of Cartilage with Adipocytokines in Juvenile Idiopathic Arthritis.

Winsz-Szczotka K, Kuznik-Trocha K, Gruenpeter A, Wojdas M, Dabkowska K, Olczyk K Metabolites. 2020; 10(2).

PMID: 32050571 PMC: 7073573. DOI: 10.3390/metabo10020061.