The imbalance between osteoprotegerin and cathepsin K in the serum of patients with longstanding rheumatoid arthritis

被引:20
作者
Skoumal, Martin [1 ,2 ,3 ]
Haberhauer, Guenther [1 ]
Kolarz, Gernot [1 ]
Hawa, Gerhard [4 ]
Woloszczuk, Wolfgang [5 ]
Klingler, Anton [6 ]
Varga, Franz [2 ,3 ]
Klaushofer, Klaus [2 ,3 ]
机构
[1] Danube Univ Krems, Inst Rheumatol Kurstadt Baden Cooperat, Baden, Austria
[2] Hanusch Hosp WGKK, Ludwig Boltzmann Inst Osteol, Dept Med 4, Vienna, Austria
[3] AUVA Trauma Ctr Meidling, Vienna, Austria
[4] Biomed Med Prod GmbH & CO KG, Vienna, Austria
[5] Ludwig Boltzmann Inst Expt Endocrinol, Vienna, Austria
[6] Univ Innsbruck Hosp, Dept Gen & Transplant Surg, Theoret Surg Unit, A-6020 Innsbruck, Austria
关键词
osteoprotegerin; receptor activator of NF-kappa B ligand; cathepsin K; rheumatoid arthritis;
D O I
10.1007/s00296-007-0506-3
中图分类号
R5 [内科学];
学科分类号
1002 [临床医学]; 100201 [内科学];
摘要
Osteoprotegerin (OPG) and soluble receptor activator of NF-kappa B ligand (sRANKL) together regulate the bone metabolism among other cytokines, whereby cathepsin K has a potent collagen-degrading activity. An imbalance of this system may be partly responsible for the skeletal complications of RA. Expanding on a previous study, we investigated the relationship between OPG, sRANKL and cathepsin K levels in the serum of patients with longstanding RA. We measured serum levels of OPG, sRANKL and cathepsin K of 100 patients with active, longstanding RA. We detected elevated serum levels of cathepsin K (median 54.8 pmol/l) and OPG (median 4.8 pmol/l), but normal sRANKL levels (median 0.2 pmol/l). Cathepsin K did not show a correlation with the overexpressed OPG (P = 0.64) and sRANKL (P = 0.81). The radiological destruction correlates significantly with cathepsin K (P = 0.004) and OPG (P = 0.007). We speculate that the increased levels of OPG are effective in compensating the action of sRANKL, but do not directly prevent bone degradation, as reflected by the elevated serum levels of cathepsin K.
引用
收藏
页码:637 / 641
页数:5
相关论文
共 30 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]
Receptor activator of NF-κB and osteoprotegerin expression by human microvascular endothelial cells, regulation by inflammatory cytokines, and role in human osteoclastogenesis [J].
Collin-Osdoby, P ;
Rothe, L ;
Anderson, F ;
Nelson, M ;
Maloney, W ;
Osdoby, P .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (23) :20659-20672
[3]
Receptor activator NF-κB ligand (RANKL) expression in synovial tissue from patients with rheumatoid arthritis, spondyloarthropathy, osteoarthritis, and from normal patients:: semiquantitative and quantitative analysis [J].
Crotti, TN ;
Smith, MD ;
Weedon, H ;
Ahern, MJ ;
Findlay, DM ;
Kraan, M ;
Tak, PP ;
Haynes, DR .
ANNALS OF THE RHEUMATIC DISEASES, 2002, 61 (12) :1047-1054
[4]
Hawa Gerhard, 2003, Clin Lab, V49, P461
[5]
Osteoprotegerin expression in synovial tissue from patients with rheumatoid arthritis, spondyloarthropathies normal controls [J].
Haynes, DR ;
Barg, E ;
Crotti, TN ;
Holding, C ;
Weedon, H ;
Atkins, GJ ;
Zannetino, A ;
Ahern, MJ ;
Coleman, M ;
Roberts-Thomson, PJ ;
Kraan, M ;
Tak, PP ;
Smith, MD .
RHEUMATOLOGY, 2003, 42 (01) :123-134
[6]
Osteoprotegerin and receptor activator of nuclear factor kappaB ligand (RANKL) regulate osteoclast formation by cells in the human rheumatoid arthritic joint [J].
Haynes, DR ;
Crotti, TN ;
Loric, M ;
Bain, GI ;
Atkins, GJ ;
Findlay, DM .
RHEUMATOLOGY, 2001, 40 (06) :623-630
[7]
Role of receptor activator of nuclear factor-κB ligand and osteoprotegerin in bone cell biology [J].
Hofbauer, LC ;
Heufelder, AE .
JOURNAL OF MOLECULAR MEDICINE-JMM, 2001, 79 (5-6) :243-253
[8]
Cleavage site specificity of cathepsin K toward cartilage proteoglycans and protease complex formation [J].
Hou, WS ;
Li, ZQ ;
Büttner, FH ;
Bartnik, E ;
Brömme, D .
BIOLOGICAL CHEMISTRY, 2003, 384 (06) :891-897
[9]
Comparison of cathepsins K and S expression within the rheumatoid and osteoarthritic synovium [J].
Hou, WS ;
Li, WJ ;
Keyszer, G ;
Weber, E ;
Levy, R ;
Klein, MJ ;
Gravallese, EM ;
Goldring, SR ;
Brömme, D .
ARTHRITIS AND RHEUMATISM, 2002, 46 (03) :663-674
[10]
Hummel KM, 1998, J RHEUMATOL, V25, P1887