Serum osteoprotegerin levels are reduced in patients with multiple myeloma with lytic bone disease

被引:129
作者
Seidel, C
Hjertner, O [1 ]
Abildgaard, N
Heickendorff, L
Hjorth, M
Westin, J
Nielsen, JL
Hjorth-Hansen, H
Waage, A
Sundan, A
Borset, M
机构
[1] Norwegian Univ Sci & Technol, Inst Canc Res & Mol Biol, MTFS, N-7489 Trondheim, Norway
[2] Norwegian Univ Sci & Technol, Univ Hosp, Dept Internal Med, Sect Hematol, N-7034 Trondheim, Norway
关键词
D O I
10.1182/blood.V98.7.2269
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Osteoprotegerin (OPG), the neutralizing decoy receptor for the osteoclast activator RANK ligand, was measured in serum taken from patients with multiple myeloma at the time of diagnosis. Median OPG was lower in the patients with myeloma (7.4 ng/mL; range, 2.6-80; n = 225) than in healthy age- and sex-matched controls (9.0 ng/mL; range 5.1-130; n = 40; P = .02). Importantly, OPG levels were associated with degree of radiographically assessed skeletal destruction (P = .01). The median OPG level in patients lacking osteolytic lesions was 9.1 ng/mL, as compared with 7.6 ng/mL and 7.0 ng/mL, respectively, in patients with minor or advanced osteolytic disease. Furthermore, OPG levels were associated with World Health Organization performance status (P = .003) and correlated to serum levels of carboxy-terminal propeptide of type I procollagen (PICP; P < .001) but not with clinical stage or survival. These findings suggest impaired OPG function in myeloma and give a rationale for OPG as a therapeutic agent against myeloma bone disease. (C) 2001 by The American Society of Hematology.
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收藏
页码:2269 / 2271
页数:3
相关论文
共 21 条
[1]   Biochemical markers of bone metabolism reflect osteoclastic and osteoblastic activity in multiple myeloma [J].
Abildgaard, N ;
Glerup, H ;
Rungby, J ;
Bendix-Hansen, K ;
Kassem, M ;
Brixen, K ;
Heickendorff, L ;
Nielsen, JL ;
Eriksen, EF .
EUROPEAN JOURNAL OF HAEMATOLOGY, 2000, 64 (02) :121-129
[2]   Serum markers of bone metabolism in multiple myeloma: Prognostic value of the carboxy-terminal telopeptide of type I collagen (ICTP) [J].
Abildgaard, N ;
Bentzen, SM ;
Nielsen, JL ;
Heickendorff, L .
BRITISH JOURNAL OF HAEMATOLOGY, 1997, 96 (01) :103-110
[3]   MECHANISMS OF BONE DESTRUCTION IN MULTIPLE-MYELOMA - THE IMPORTANCE OF AN UNBALANCED PROCESS IN DETERMINING THE SEVERITY OF LYTIC BONE-DISEASE [J].
BATAILLE, R ;
CHAPPARD, D ;
MARCELLI, C ;
DESSAUW, P ;
SANY, J ;
BALDET, P ;
ALEXANDRE, C .
JOURNAL OF CLINICAL ONCOLOGY, 1989, 7 (12) :1909-1914
[4]   RECRUITMENT OF NEW OSTEOBLASTS AND OSTEOCLASTS IS THE EARLIEST CRITICAL EVENT IN THE PATHOGENESIS OF HUMAN MULTIPLE-MYELOMA [J].
BATAILLE, R ;
CHAPPARD, D ;
MARCELLI, C ;
DESSAUW, P ;
BALDET, P ;
SANY, J ;
ALEXANDRE, C .
JOURNAL OF CLINICAL INVESTIGATION, 1991, 88 (01) :62-66
[5]  
Borset M, 2000, BLOOD, V96, P2528
[6]  
DURIE BGM, 1975, CANCER, V36, P842, DOI 10.1002/1097-0142(197509)36:3<842::AID-CNCR2820360303>3.0.CO
[7]  
2-U
[8]   Transmembrane and cytoplasmic domains of syndecan mediate a multi-step endocytic pathway involving detergent-insoluble membrane rafts [J].
Fuki, IV ;
Meyer, ME ;
Williams, KJ .
BIOCHEMICAL JOURNAL, 2000, 351 (03) :607-612
[9]   The syndecan family of proteoglycans - Novel receptors mediating internalization of atherogenic lipoproteins in vitro [J].
Fuki, IV ;
Kuhn, KM ;
Lomazov, IR ;
Rothman, VL ;
Tuszynski, GP ;
Iozzo, RV ;
Swenson, TL ;
Fisher, EA ;
Williams, KJ .
JOURNAL OF CLINICAL INVESTIGATION, 1997, 100 (06) :1611-1622
[10]  
Hjertner O, 1999, BLOOD, V94, P3883