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Biological markers in osteoarthritis

机译:骨关节炎的生物标志物

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Osteoarthritis (OA) is considered as a chronic disease with a long "silent" period. The diagnosis is generally based on clinical symptoms and radiographic changes. However X-ray has a poor sensitivity and a relatively large precision error that does not allow an early detection of OA or the monitoring of joint damage progression. The limitations of the tools that are currently available for OA assessment have been the impetus to identify specific biological markers that reflect quantitative and dynamic variations in joint remodeling. Research has focused on the structural components of cartilage matrix, especially type II collagen degradation markers. In spite of a significant increase of some markers in individuals with early stage of OA, the large overlap with control subjects indicates that the current biomarkers used alone have limited diagnostic potential. However, the combination of specific markers seems to improve the prediction of disease progression at the individual level. Several types of treatment have been investigated but the lack of medications with definitively demonstrated chondroprotective activity has limited the assessment of the potential role of biomarkers for monitoring patients' responses to the treatment of OA. In this review, we will use the BIPED classification that appeared in 2006 for OA markers to describe the potential usage of a given marker [5].This article is part of a Special Issue entitled "Osteoarthritis".
机译:骨关节炎(OA)被认为是一种长期的“沉默”期的慢性疾病。诊断通常基于临床症状和影像学改变。但是,X射线的灵敏度较差且精度误差较大,因此无法及早发现OA或监测关节损伤的进展。目前可用于OA评估的工具的局限性是推动人们确定能够反映关节重塑中定量和动态变化的特定生物学标记的动力。研究集中在软骨基质的结构成分上,尤其是II型胶原降解标记物。尽管OA早期个体中某些标志物显着增加,但与对照受试者的大量重叠表明,单独使用当前的生物标志物具有有限的诊断潜力。但是,特定标志物的组合似乎可以改善个体水平上疾病进展的预测。已经研究了几种类型的治疗方法,但是缺乏明确证实的软骨保护活性的药物,限制了对生物标记物监测患者对OA治疗反应的潜在作用的评估。在本文中,我们将使用2006年出现的OA标记物的BIPED分类来描述特定标记物的潜在用途[5]。本文是名为“骨关节炎”的特刊的一部分。

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