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肿瘤坏死因子拮抗剂可改善类风湿关节炎的疾病活动度,但不能改善动脉僵硬度。

Tumour necrosis factor antagonists improve disease activity but not arterial stiffness in rheumatoid arthritis.

作者信息

Van Doornum S, McColl G, Wicks I P

机构信息

Department of Medicine (RMH/WH), The University of Melbourne, Post Office, Royal Melbourne Hospital, Victoria 3050 Australia.

出版信息

Rheumatology (Oxford). 2005 Nov;44(11):1428-32. doi: 10.1093/rheumatology/kei033. Epub 2005 Aug 2.

Abstract

OBJECTIVES

Systemic inflammation may play an important role in the accelerated atherosclerosis and increased cardiovascular mortality of rheumatoid arthritis (RA). Atorvastatin reduced arterial stiffness in RA patients after only 6 weeks, an effect that may be partially mediated by the immunomodulatory effects of this drug. Suppression of inflammation with tumour necrosis factor (TNF) antagonists may therefore also improve vascular function in RA; however, TNF antagonists have also been shown to cause or exacerbate congestive heart failure in patients with RA and heart failure. The aim of the present study was to examine the effect of treatment with TNF antagonists on arterial stiffness in RA patients with active disease.

METHODS

Fourteen RA patients (age 55.1 +/- 3.8 yr; disease duration 7.9 +/- 1.3 yr) with high disease activity [disease activity score (DAS28) 7.1 +/- 0.3] commencing treatment with TNF antagonists for the first time were studied. Clinical status and arterial stiffness were measured before and after 6 weeks of TNF antagonist therapy (etanercept, adalimumab or infliximab).

RESULTS

Arterial stiffness did not change during the study period (the mean augmentation index was 29.1 +/- 2.2% at baseline vs 30.1 +/- 1.8% at week 6; P = 0.504). The DAS28 improved significantly from 7.1 +/- 0.3 to 4.3 +/- 0.4 (P < 0.0001). The erythrocyte sedimentation rate and C-reactive protein [median (range)] were reduced from 44 (12-85) to 15 (3-82) mm/h (P = 0.02) and from 34 (3-95) to 10 (2-61) mg/l (P = 0.007), respectively.

CONCLUSIONS

Despite significant reductions in synovitis and inflammatory markers in these RA patients, arterial stiffness was not improved by 6 weeks of treatment with TNF antagonists. This result is of relevance given recent reports of potential adverse cardiovascular effects of TNF antagonists in some RA patients.

摘要

目的

全身炎症可能在类风湿关节炎(RA)患者动脉粥样硬化加速及心血管死亡率增加中起重要作用。阿托伐他汀仅在6周后就能降低RA患者的动脉僵硬度,这一作用可能部分由该药物的免疫调节作用介导。因此,用肿瘤坏死因子(TNF)拮抗剂抑制炎症也可能改善RA患者的血管功能;然而,TNF拮抗剂也已被证明会导致或加重RA合并心力衰竭患者的充血性心力衰竭。本研究的目的是探讨TNF拮抗剂治疗对活动性疾病的RA患者动脉僵硬度的影响。

方法

研究了14例首次开始使用TNF拮抗剂治疗的高疾病活动度[疾病活动评分(DAS28)为7.1±0.3]的RA患者(年龄55.1±3.8岁;病程7.9±1.3年)。在TNF拮抗剂治疗(依那西普、阿达木单抗或英夫利昔单抗)6周前后测量临床状态和动脉僵硬度。

结果

在研究期间动脉僵硬度未发生变化(基线时平均增强指数为29.1±2.2%,第6周时为30.1±1.8%;P = 0.504)。DAS28从7.1±0.3显著改善至4.3±0.4(P < 0.0001)。红细胞沉降率和C反应蛋白[中位数(范围)]分别从44(12 - 85)降至15(3 - 82)mm/h(P = 0.02)和从34(3 - 95)降至10(2 - 61)mg/l(P = 0.007)。

结论

尽管这些RA患者的滑膜炎和炎症标志物显著降低,但TNF拮抗剂治疗6周并未改善动脉僵硬度。鉴于最近有报道称TNF拮抗剂在一些RA患者中可能产生潜在的不良心血管影响,这一结果具有重要意义。

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