首页> 外文期刊>Scandinavian journal of rheumatology >Circulating levels of osteopontin, osteoprotegerin, total soluble receptor activator of nuclear factor-kappa B ligand, and high-sensitivity C-reactive protein in patients with active rheumatoid arthritis randomized to etanercept alone or in combination with methotrexate
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Circulating levels of osteopontin, osteoprotegerin, total soluble receptor activator of nuclear factor-kappa B ligand, and high-sensitivity C-reactive protein in patients with active rheumatoid arthritis randomized to etanercept alone or in combination with methotrexate

机译:单独或依那西普或联合氨甲蝶呤治疗的活动性类风湿性关节炎患者的骨桥蛋白,骨保护素,核因子-κB配体的总可溶性受体激活剂和高敏C反应蛋白的循环水平

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OBJECTIVE: To determine whether circulating levels of osteopontin (OPN), osteoprotegerin (OPG), total soluble receptor activator of nuclear factor-kappa B ligand (total sRANKL), and high-sensitivity C-reactive protein (hsCRP) change in patients with rheumatoid arthritis (RA) during immunosuppressive therapy. METHODS: Twenty-five active RA patients were randomized to treatment with either etanercept alone or in combination with methotrexate (MTX). The treatment response after 16 weeks was assessed using the European League Against Rheumatism (EULAR) response criteria. Blood samples were taken before the start of and every fourth week during the study. OPN, OPG, and total sRANKL were measured by enzyme-linked immunosorbent assays (ELISAs) and hsCRP by highly sensitive turbidometry. RESULTS: At baseline, OPN and hsCRP were significantly (p<0.001) elevated compared to healthy persons. Compared to baseline only hsCRP levels decreased significantly (p<0.05 to p<0.001) in the EULAR responders through the study. OPN remained significantly (p<0.05) elevated at 16 weeks in patients with a low disease activity score (DAS< or =3.2). Total sRANKL increased significantly (p<0.05) from baseline to week 12. No statistically significant changes were observed in the non-responders. CONCLUSION: Active RA patients showed increased circulating levels of hsCRP and OPN, but only hsCRP decreased during etanercept therapy. Our findings suggest that OPN, OPG, total sRANKL, and hsCRP reflect different aspects of the inflammatory process in RA.
机译:目的:确定类风湿患者的骨桥蛋白(OPN),骨保护素(OPG),核因子-κB配体的总可溶性受体激活剂(总sRANKL)和高敏C反应蛋白(hsCRP)的循环水平是否发生变化免疫抑制治疗期间的关节炎(RA)。方法:25例活动性RA患者被随机分配接受依那西普单独治疗或与甲氨蝶呤(MTX)联合治疗。使用欧洲抗风湿病联盟(EULAR)响应标准评估16周后的治疗响应。在研究开始之前以及研究过程中的第四个星期采集血液样本。 OPN,OPG和总sRANKL通过酶联免疫吸附测定(ELISA)和hsCRP通过高灵敏度浊度法进行测量。结果:与健康人相比,基线时OPN和hsCRP显着升高(p <0.001)。与基线相比,EULAR应答者中仅hsCRP水平显着降低(p <0.05至p <0.001)。在疾病活动评分低(DAS <或= 3.2)的患者中,OPN在16周时仍显着升高(p <0.05)。从基线到第12周,总sRANKL显着增加(p <0.05),在无反应者中未观察到统计学上的显着变化。结论:活跃的RA患者表现出hsCRP和OPN的循环水平升高,但依那西普治疗期间仅hsCRP降低。我们的发现表明OPN,OPG,总sRANKL和hsCRP反映了RA炎症过程的不同方面。

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