Lorenz Helga, Richter Wiltrud
Stiftung Orthopädische Universitätsklinik Heidelberg, Sektion Experimentelle Orthopädie, Schlierbacher Landstrasse 200a, 69118 Heidelberg, Germany.
Prog Histochem Cytochem. 2006;40(3):135-63. doi: 10.1016/j.proghi.2006.02.003. Epub 2006 Mar 23.
Osteoarthritis (OA) is a disease of high ethical and economical importance. In advanced stages, the patients suffer from severe pain and restriction of mobility. The consequence in many cases is an inability to work and often the substitution of the diseased joint with an artificial implant becomes inevitable. As cartilage tissue itself has only very limited capacities of self-renewing, the development of this disorder is chronic and progressive. Generally, OA is diagnosed in more advanced stages, when clinical and radiographic signs become evident. At this time point the options for therapeutic intervention without surgery are limited. It is, therefore, crucial to know about the basic incidents in the course of OA and especially in early stages to develop new diagnostic and therapeutic strategies. Numerous studies on human osteoarthritic tissue and in animal models have addressed various aspects of OA progression to get a better understanding of the pathophysiology of this disease. This review presents an overview on different aspects of OA research and the cellular and molecular alterations in degenerating cartilage.
骨关节炎(OA)是一种具有高度伦理和经济重要性的疾病。在晚期,患者会遭受严重疼痛和行动受限。在许多情况下,后果是无法工作,而且往往不可避免地要用人工植入物替换患病关节。由于软骨组织本身的自我更新能力非常有限,这种疾病的发展是慢性且渐进性的。一般来说,OA在更晚期才被诊断出来,此时临床和影像学症状才会明显。在这个时间点,非手术治疗干预的选择有限。因此,了解OA病程中的基本事件,尤其是早期事件,对于制定新的诊断和治疗策略至关重要。关于人类骨关节炎组织和动物模型的大量研究已经探讨了OA进展的各个方面,以便更好地理解这种疾病的病理生理学。本综述概述了OA研究的不同方面以及退化软骨中的细胞和分子变化。