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短期使用阿达木单抗治疗可改善对英夫利昔单抗难治的类风湿关节炎患者的内皮功能。

Short-term adalimumab therapy improves endo-thelial function in patients with rheumatoid arthritis refractory to infliximab.

作者信息

Gonzalez-Juanatey C, Llorca J, Sanchez-Andrade A, Garcia-Porrua C, Martin J, Gonzalez-Gay M A

机构信息

Cardiology, Hospital Xeral-Calde, Lugo, Spain.

出版信息

Clin Exp Rheumatol. 2006 May-Jun;24(3):309-12.

Abstract

OBJECTIVE

Endothelial dysfunction has been found in patients with rheumatoid arthritis (RA). In this study we aimed to assess whether adalimumab, a fully human monoclonal antibody directed against TNF-alpha, was able to improve endothelial function in RA patients with long-standing disease refractory to infliximab.

METHODS

Eight RA patients (7 women; range: 24- 74 years) were studied. They had been treated with the chimeric monoclonal anti-TNF-alpha antibody-infliximab for at least 1 year and were switched to adalimumab therapy because of loss of efficacy following periodical treatment with infliximab. Endothelial dependent (EDV) and independent vasodilatation (EIV) were measured by brachial ultrasonography. Patients were assessed prior to (day 0) and at day 2, and weeks 2 and 12 after the onset of adalimumab therapy.

RESULTS

Following adalimumab administration a rapid increase in the percentage (%) of EDV was found in all patients (mean +/- SD: 10.1 +/- 5.1% at day 2 compared to 5.8 +/- 4.1% at day 0). At weeks 2 and 12 the %EDV was also significantly increased compared to day 0. All patients showed decrease in the disease activity score 28 and C-reactive protein levels (P = 0.012). Moreover, at week 12 the atherogenic index was reduced in all patients (P = 0.012).

CONCLUSION

Our study confirms that short-term adalimumab therapy yields an active and positive effect on endothelial function in long-standing RA patients with severe disease. This observation emphasizes the potential role of the TNF-alpha blockade in the mechanisms implicated in the development of atherogenesis in RA.

摘要

目的

类风湿关节炎(RA)患者中已发现存在内皮功能障碍。在本研究中,我们旨在评估阿达木单抗(一种针对肿瘤坏死因子-α的全人单克隆抗体)是否能够改善对英夫利昔单抗耐药的长期RA患者的内皮功能。

方法

研究了8例RA患者(7例女性;年龄范围:24 - 74岁)。他们接受嵌合单克隆抗肿瘤坏死因子-α抗体英夫利昔单抗治疗至少1年,因英夫利昔单抗定期治疗后疗效丧失而改用阿达木单抗治疗。通过肱动脉超声测量内皮依赖性(EDV)和非内皮依赖性血管舒张(EIV)。在阿达木单抗治疗开始前(第0天)、第2天以及治疗开始后第2周和第12周对患者进行评估。

结果

给予阿达木单抗后,所有患者的内皮依赖性血管舒张百分比(%)迅速增加(平均±标准差:第2天为10.1±5.1%,而第0天为5.8±4.1%)。与第0天相比,第2周和第12周时内皮依赖性血管舒张百分比也显著增加。所有患者的疾病活动评分28和C反应蛋白水平均下降(P = 0.012)。此外,在第12周时所有患者的动脉粥样硬化指数均降低(P = 0.012)。

结论

我们的研究证实,短期阿达木单抗治疗对患有严重疾病的长期RA患者的内皮功能产生积极且正向的作用。这一观察结果强调了肿瘤坏死因子-α阻断在RA动脉粥样硬化发生机制中的潜在作用。

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