New York University School of Medicine, and Hospital for Joint Diseases at NYU Langone Medical Center, New York, New York 10003, USA.
Curr Opin Rheumatol. 2013 Jan;25(1):136-44. doi: 10.1097/BOR.0b013e32835a9381.
Identification of patients at risk for incident disease or disease progression in osteoarthritis remains challenging, as radiography is an insensitive reflection of molecular changes that presage cartilage and bone abnormalities. Thus there is a widely appreciated need for biochemical and imaging biomarkers. We describe recent developments with such biomarkers to identify osteoarthritis patients who are at risk for disease progression.
The biochemical markers currently under evaluation include anabolic, catabolic, and inflammatory molecules representing diverse biological pathways. A few promising cartilage and bone degradation and synthesis biomarkers are in various stages of development, awaiting further validation in larger populations. A number of studies have shown elevated expression levels of inflammatory biomarkers, both locally (synovial fluid) and systemically (serum and plasma). These chemical biomarkers are under evaluation in combination with imaging biomarkers to predict early onset and the burden of disease.
Prognostic biomarkers may be used in clinical knee osteoarthritis to identify subgroups in whom the disease progresses at different rates. This could facilitate our understanding of the pathogenesis and allow us to differentiate phenotypes within a heterogeneous knee osteoarthritis population. Ultimately, such findings may help facilitate the development of disease-modifying osteoarthritis drugs (DMOADs).
在骨关节炎中,识别有新发病或疾病进展风险的患者仍然具有挑战性,因为放射影像学对预示软骨和骨骼异常的分子变化的反映不敏感。因此,人们普遍认识到需要生物化学和影像学生物标志物。我们描述了这些生物标志物的最新进展,以识别有疾病进展风险的骨关节炎患者。
目前正在评估的生化标志物包括代表不同生物学途径的合成代谢、分解代谢和炎症分子。一些有前途的软骨和骨降解和合成生物标志物处于不同的开发阶段,有待在更大的人群中进一步验证。许多研究表明,局部(滑液)和全身(血清和血浆)的炎症生物标志物的表达水平升高。这些化学生物标志物正在与影像学生物标志物一起评估,以预测疾病的早期发作和疾病负担。
预后生物标志物可用于膝关节骨关节炎的临床治疗,以识别疾病进展速度不同的亚组。这可以帮助我们了解发病机制,并允许我们在异质性膝关节骨关节炎人群中区分表型。最终,这些发现可能有助于促进疾病修饰性骨关节炎药物(DMOADs)的开发。