Department of Biomedicine, Institute of Medical Biotechnology, Ministry of Education and Sciences, Tbilisi, Georgia.
Osteoarthritis Cartilage. 2010 Nov;18(11):1448-53. doi: 10.1016/j.joca.2010.06.009. Epub 2010 Jul 13.
The aim of the study was to evaluate the association between prevalence and severity of radiographic hand osteoarthritis (OA) and serum levels of systemic inflammatory markers in a community-based population sample.
A cross-sectional observational study was conducted on a population comprised 1452 Chuvashians (763 males, aged 49.23 ± 17.43; and 689 females, aged 50.37 ± 17.47 years). OA was evaluated in 14 joints of each hand using Kellgren and Lawrence (K-L), joint space narrowing (JSN) and osteophyte (OS) scores. Serum levels of systemic inflammatory and osteoclastogenic cytokines were measured by an enzyme-linked immunosorbent assay (ELISA). Statistical analyses included descriptive statistics, correlation analysis and multiple linear regressions.
Monocyte chemotactic protein-1 (MCP-1) and osteoprotegerin (OPG) levels were associated with OA traits, but the statistically significant correlations were weak and/or moderate. In particular, the MCP-1 inflammation marker showed a statistically significant association with JSN (β=0.077, P=0.022) and OS (β=0.067, P=0.024) scores, but not with the number of affected joints (K-L ≥ 2). OPG was significantly correlated with the scores as to the number of affected joints (β=0.063, P=0.035) and OS (β=0.077, P=0.028). No significant associations were found between levels of other inflammatory [interleukin (IL)-6, tumor necrosis factor (TNF)-α, IL-17] and osteoclastogenic [receptor activator for nuclear factor κ B ligand (RANKL), macrophage colony-stimulating factor (M-CSF)] cytokines and OA characteristics.
This study strengthens the premise that OPG might be a valid biomarker of hand OA. Confirmation of these results in larger cohorts of patients will reinforce our theory that the RANKL/OPG pathway is a suitable target for developing novel agents against OA.
本研究旨在评估在基于社区的人群样本中,影像学手部骨关节炎(OA)的患病率和严重程度与血清系统炎症标志物水平之间的相关性。
对 1452 名楚瓦什人(763 名男性,年龄 49.23±17.43 岁;689 名女性,年龄 50.37±17.47 岁)进行了一项横断面观察性研究。使用 Kellgren 和 Lawrence(K-L)、关节间隙狭窄(JSN)和骨赘(OS)评分评估双手 14 个关节的 OA。通过酶联免疫吸附试验(ELISA)测量血清系统炎症和破骨细胞生成细胞因子的水平。统计分析包括描述性统计、相关性分析和多元线性回归。
单核细胞趋化蛋白-1(MCP-1)和骨保护素(OPG)水平与 OA 特征相关,但统计学上显著的相关性较弱且/或中等。具体而言,MCP-1 炎症标志物与 JSN(β=0.077,P=0.022)和 OS(β=0.067,P=0.024)评分呈统计学显著相关,但与受影响关节数量无关(K-L≥2)。OPG 与受影响关节数量(β=0.063,P=0.035)和 OS(β=0.077,P=0.028)评分显著相关。其他炎症细胞因子(白细胞介素(IL)-6、肿瘤坏死因子(TNF)-α、IL-17)和破骨细胞生成细胞因子(核因子κ B 受体激活剂配体(RANKL)、巨噬细胞集落刺激因子(M-CSF))的水平与 OA 特征之间未发现显著相关性。
本研究进一步证实了 OPG 可能是手部 OA 的有效生物标志物。在更大的患者队列中确认这些结果将加强我们的理论,即 RANKL/OPG 途径是开发针对 OA 的新型药物的合适靶点。