Subchondral bone as a key target for osteoarthritis treatment

被引:200
作者
Castaneda, Santos [1 ]
Roman-Blas, Jorge A. [2 ]
Largo, Raquel [2 ]
Herrero-Beaumont, Gabriel [2 ]
机构
[1] Univ Autonoma Madrid, IIS Princesa, Hosp La Princesa, Dept Rheumatol, Madrid, Spain
[2] Univ Autonoma Madrid, IIS FJD, Fdn Jimenez Diaz, Bone & Joint Res Unit,Serv Rheumatol, Madrid, Spain
关键词
Subchondral bone; Osteoarthritis; Pathogenesis; Antiresorptives; New therapies; ANTERIOR CRUCIATE LIGAMENT; ESTROGEN REPLACEMENT THERAPY; MENISCECTOMIZED GUINEA-PIG; KNEE OSTEOARTHRITIS; ARTICULAR-CARTILAGE; STRONTIUM RANELATE; PROSTAGLANDIN E-2; SALMON-CALCITONIN; TRABECULAR BONE; MINERAL DENSITY;
D O I
10.1016/j.bcp.2011.09.018
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Osteoarthritis (OA), the most common form of arthritis, is a debilitating and progressive disease that has become a major cause of disability and impaired quality of life in the elderly. OA is considered an organ disease that affects the whole joint, where the subchondral bone (SB) plays a crucial role. Regardless of whether SB alterations precede cartilage damage or appear during the evolution of the disease, SB is currently recognised as a key target in OA treatment. In fact, bone abnormalities, especially increased bone turnover, have been detected in the early evolution of some forms of OA. Systemic osteoporosis (OP) and OA share a paradoxical relationship in which both high and low bone mass conditions may result in induction and/or OA progression. Recent findings suggest that some drugs may be useful in treating both processes simultaneously, at least in a subgroup of patients with OA and OP. This review focuses on the role of SB in OA pathogenesis, describing relevant underlying mechanisms involved in the process and examining the potential activity as disease-modifying anti-osteoarthritic drugs (DMOADs) of certain SB-targeting agents currently under study. (C) 2011 Elsevier Inc. All rights reserved.
引用
收藏
页码:315 / 323
页数:9
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