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一项关于甲氨蝶呤治疗银屑病关节炎的随机安慰剂对照试验。

A randomized placebo-controlled trial of methotrexate in psoriatic arthritis.

作者信息

Kingsley Gabrielle H, Kowalczyk Anna, Taylor Helen, Ibrahim Fowzia, Packham Jonathan C, McHugh Neil J, Mulherin Diarmuid M, Kitas George D, Chakravarty Kuntal, Tom Brian D M, O'Keeffe Aidan G, Maddison Peter J, Scott David L

机构信息

Department of Rheumatology, King's College London School of Medicine, King's College London, London SE5 9RJ, UK.

出版信息

Rheumatology (Oxford). 2012 Aug;51(8):1368-77. doi: 10.1093/rheumatology/kes001. Epub 2012 Feb 17.

Abstract

OBJECTIVE

MTX is widely used to treat synovitis in PsA without supporting trial evidence. The aim of our study was to test the value of MTX in the first large randomized placebo-controlled trial (RCT) in PsA.

METHODS

A 6-month double-blind RCT compared MTX (15 mg/week) with placebo in active PsA. The primary outcome was PsA response criteria (PsARC). Other outcomes included ACR20, DAS-28 and their individual components. Missing data were imputed using multiple imputation methods. Treatments were compared using logistic regression analysis (adjusted for age, sex, disease duration and, where appropriate, individual baseline scores).

RESULTS

Four hundred and sixty-two patients were screened and 221 recruited. One hundred and nine patients received MTX and 112 received placebo. Forty-four patients were lost to follow-up (21 MTX, 23 placebo). Twenty-six patients discontinued treatment (14 MTX, 12 placebo). Comparing MTX with placebo in all randomized patients at 6 months showed no significant effect on PsARC [odds ratio (OR) 1.77, 95% CI 0.97, 3.23], ACR20 (OR 2.00, 95% CI 0.65, 6.22) or DAS-28 (OR 1.70, 95% CI 0.90, 3.17). There were also no significant treatment effects on tender and swollen joint counts, ESR, CRP, HAQ and pain. The only benefits of MTX were reductions in patient and assessor global scores and skin scores at 6 months (P = 0.03, P < 0.001 and P = 0.02, respectively). There were no unexpected adverse events.

CONCLUSIONS

This trial of active PsA found no evidence for MTX improving synovitis and consequently raises questions about its classification as a disease-modifying drug in PsA. Trial registration. Current Controlled Trials, www.controlled-trials.com, ISRCTN:54376151.

摘要

目的

甲氨蝶呤(MTX)广泛用于治疗银屑病关节炎(PsA)的滑膜炎,但缺乏试验证据支持。我们研究的目的是在首个针对PsA的大型随机安慰剂对照试验(RCT)中检验MTX的价值。

方法

一项为期6个月的双盲RCT比较了MTX(15毫克/周)与安慰剂治疗活动性PsA的效果。主要结局是PsA缓解标准(PsARC)。其他结局包括美国风湿病学会20%改善标准(ACR20)、疾病活动度评分28(DAS-28)及其各个组成部分。使用多重填补方法对缺失数据进行填补。采用逻辑回归分析比较治疗效果(校正年龄、性别、病程,并在适当情况下校正个体基线评分)。

结果

共筛查462例患者,招募221例。109例患者接受MTX治疗,112例接受安慰剂治疗。44例患者失访(21例MTX组,23例安慰剂组)。26例患者停止治疗(14例MTX组,12例安慰剂组)。在所有随机分组的患者中,6个月时比较MTX与安慰剂,结果显示对PsARC[比值比(OR)1.77,95%置信区间(CI)0.97,3.23]、ACR20(OR 2.00,95%CI 0.65,6.22)或DAS-28(OR 1.70,95%CI 0.90,3.17)均无显著影响。对压痛和肿胀关节计数、红细胞沉降率(ESR)、C反应蛋白(CRP)、健康评估问卷(HAQ)和疼痛也无显著治疗效果。MTX唯一的益处是在6个月时患者和评估者的整体评分以及皮肤评分有所降低(分别为P = 0.03、P < 0.001和P = 0.02)。未发生意外不良事件。

结论

这项针对活动性PsA的试验未发现MTX能改善滑膜炎的证据,因此对其作为PsA中改善病情药物的分类提出了质疑。试验注册。当前对照试验,www.controlled-trials.com,国际标准随机对照试验编号:54376151。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1419/3397466/3f23d9d52c2e/kes001f1.jpg

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