Serum levels of cartilage oligomeric matrix protein - A predicting factor and a valuable parameter for disease management in rheumatoid arthritis

被引:50
作者
Skoumal, M
Kolarz, G
Klingler, A
机构
[1] Rheumasonderkrankenanstalt SVA Gewerblichen Wirts, AT-2500 Baden, Austria
[2] Donau Univ Krems, Inst Rheumatol Kurstadt Baden, Baden, Austria
[3] Univ Hosp, Theoret Surg Unit, Dept Gen & Transplant Surg, Innsbruck, Austria
关键词
serum levels of COMP; rheumatoid arthritis; predicting factor;
D O I
10.1080/03009740310002498
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective: To examine whether cartilage oligomeric matrix protein (COMP) correlates with inflammation and/or joint destruction of patients with rheumatoid arthritis (RA) and to test COMP as predicting factor for the outcome of patients with established RA. Methods: Serum levels of COMP were measured in sera of 62 patients, suffering from RA according to the ACR criteria and treated in intervals in our department, over a period of 5 years. A commercially available sandwich-type ELISA-kit developed by AnaMar Medical AB, Sweden, was used. The results of serum COMP were compared with the Disease Activity Score (DAS), the Larsen Score, and clinical and laboratory parameters. Results: We found a positive correlation between serum levels of COMP at baseline and deterioration of Larsen score even after 5 years (p<0.007; r=0.34). To confirm serum COMP as an independent predicting factor for patients with RA we looked at a subgroup of patients (n=17) with elevated serum levels of COMP (mean 11,7 U/l) and low clinical prognostic factors. In this subgroup we also found a significant correlation with delta Larsen score (p<0.01; r=0.59) after 5 years. Conclusion: Serum levels of COMP is known to reflect increased cartilage turnover. The results indicate that serum COMP may be used as a prognostic marker of cartilage degradation in a patient group with established RA.
引用
收藏
页码:156 / 161
页数:6
相关论文
共 53 条
[1]   THE AMERICAN-RHEUMATISM-ASSOCIATION 1987 REVISED CRITERIA FOR THE CLASSIFICATION OF RHEUMATOID-ARTHRITIS [J].
ARNETT, FC ;
EDWORTHY, SM ;
BLOCH, DA ;
MCSHANE, DJ ;
FRIES, JF ;
COOPER, NS ;
HEALEY, LA ;
KAPLAN, SR ;
LIANG, MH ;
LUTHRA, HS ;
MEDSGER, TA ;
MITCHELL, DM ;
NEUSTADT, DH ;
PINALS, RS ;
SCHALLER, JG ;
SHARP, JT ;
WILDER, RL ;
HUNDER, GG .
ARTHRITIS AND RHEUMATISM, 1988, 31 (03) :315-324
[2]  
ARNOLD MH, 1990, BRIT J RHEUMATOL, V29, P120
[3]  
Arvidson NG, 2002, SCAND J RHEUMATOL, V31, P146
[4]  
Clark AG, 1999, ARTHRITIS RHEUM, V42, P2356, DOI 10.1002/1529-0131(199911)42:11<2356::AID-ANR14>3.0.CO
[5]  
2-R
[6]   Expression of cartilage oligomeric matrix protein (COMP) by embryonic and adult osteoblasts [J].
Di Cesare, PE ;
Fang, C ;
Leslie, MP ;
Tulli, H ;
Perris, R ;
Carlson, CS .
JOURNAL OF ORTHOPAEDIC RESEARCH, 2000, 18 (05) :713-720
[7]  
Di Cesare PE, 1999, J ORTHOPAED RES, V17, P437
[8]   Increased degradation and altered tissue distribution of cartilage oligomeric matrix protein in human rheumatoid and osteoarthritic cartilage [J].
DiCesare, PE ;
Carlson, CS ;
Stolerman, ES ;
Hauser, N ;
Tulli, H ;
Paulsson, M .
JOURNAL OF ORTHOPAEDIC RESEARCH, 1996, 14 (06) :946-955
[9]   Expression of cartilage oligomeric matrix protein by human synovium [J].
DiCesare, PE ;
Carlson, CS ;
Stollerman, ES ;
Chen, FS ;
Leslie, M ;
Perris, R .
FEBS LETTERS, 1997, 412 (01) :249-252
[10]  
FORSLIND K, 1992, BRIT J RHEUMATOL, V31, P593