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随机接受单独使用依那西普或联合甲氨蝶呤治疗的活动性类风湿关节炎患者血清骨桥蛋白、骨保护素、核因子κB受体活化因子配体总可溶性受体及高敏C反应蛋白水平

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.

作者信息

Sennels Hp, Sørensen S, Ostergaard M, Knudsen Ls, Hansen Ms, Skjødt H, Peters Nd, Colic A, Grau K, Jacobsen S

机构信息

Department of Clinical Biochemistry, Hvidovre Hospital, Copenhagen University Hospital, Hvidovre, Denmark.

出版信息

Scand J Rheumatol. 2008 Jul-Aug;37(4):241-7. doi: 10.1080/03009740801910320.

DOI:10.1080/03009740801910320
PMID:18612923
Abstract

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.

摘要

目的

确定类风湿关节炎(RA)患者在免疫抑制治疗期间骨桥蛋白(OPN)、骨保护素(OPG)、核因子-κB 配体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。

方法

25 例活动期 RA 患者被随机分为单独使用依那西普或与甲氨蝶呤(MTX)联合治疗。使用欧洲抗风湿病联盟(EULAR)反应标准评估 16 周后的治疗反应。在研究开始前和研究期间每四周采集血样。通过酶联免疫吸附测定(ELISA)测量 OPN、OPG 和总 sRANKL,通过高敏比浊法测量 hsCRP。

结果

在基线时,与健康人相比,OPN 和 hsCRP 显著升高(p<0.001)。与基线相比,在整个研究过程中,EULAR 反应者中只有 hsCRP 水平显著降低(p<0.05 至 p<0.001)。疾病活动评分低(DAS≤3.2)的患者在 16 周时 OPN 仍显著升高(p<0.05)。从基线到第 12 周,总 sRANKL 显著增加(p<0.05)。在无反应者中未观察到统计学上的显著变化。

结论

活动期 RA 患者显示 hsCRP 和 OPN 的循环水平升高,但在依那西普治疗期间只有 hsCRP 降低。我们的研究结果表明,OPN、OPG、总 sRANKL 和 hsCRP 反映了 RA 炎症过程的不同方面。

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