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多生物标志物疾病活动评分可追踪类风湿关节炎患者对利妥昔单抗治疗的反应:三项队列研究的事后分析。

The multi-biomarker disease activity score tracks response to rituximab treatment in rheumatoid arthritis patients: a post hoc analysis of three cohort studies.

机构信息

Department of Rheumatology & Clinical Immunology, University Medical Center Utrecht, Heidelberglaan 100, 3508 GA, Utrecht, The Netherlands.

Department of Biochemistry, The James Cook University Hospital, Marton Road, Middlesborough, TS4 3BW, UK.

出版信息

Arthritis Res Ther. 2018 Nov 20;20(1):256. doi: 10.1186/s13075-018-1750-5.

Abstract

BACKGROUND

A multi-biomarker disease activity (MBDA) score has been validated as an objective measure of disease activity in rheumatoid arthritis (RA) and shown to track response to treatment with several disease-modifying anti-rheumatic drugs (DMARDs). The objective of this study was to evaluate the ability of the MBDA score to track response to treatment with rituximab.

METHODS

Data were used from 57 RA patients from three cohorts treated with rituximab 1000 mg and methylprednisolone 100 mg at days 1 and 15. The MBDA score was assessed in serum samples obtained at baseline and 6 months. Spearman's rank correlation coefficients were calculated for baseline values, 6-month values, and change from baseline to 6 months (∆), between MBDA score and the following measures: disease activity score assessing 28 joints (DAS28) using erythrocyte sedimentation rate (ESR) or high-sensitivity C-reactive protein (hsCRP), ESR, (hs)CRP, swollen and tender joint counts assessing 28 joints (SJC28, TJC28), patient visual analogue scale for general health (VAS-GH), health assessment questionnaire (HAQ), and radiographic progression over 12 months using Sharp/van der Heijde score (SHS), as well as six bone turnover markers. Additionally, multivariable linear regression analyses were performed using these measures as dependent variable and the MBDA score as independent variable, with adjustment for relevant confounders. The association between ∆MBDA score and European League Against Rheumatism (EULAR) response at 6 months was assessed with adjustment for relevant confounders.

RESULTS

At baseline, the median MBDA score and DAS28-ESR were 54.0 (IQR 44.3-70.0) and 6.3 (IQR 5.4-7.1), respectively. MBDA scores correlated significantly with DAS28-ESR, DAS28-hsCRP, ESR and (hs)CRP at baseline and 6 months. ∆MBDA score correlated significantly with changes in these measures. ∆MBDA score was associated with EULAR good or moderate response (adjusted OR = 0.89, 95% CI = 0.81-0.98, p = 0.02). Neither baseline MBDA score nor ΔMBDA score correlated statistically significantly with ∆SHS (n = 11) or change in bone turnover markers (n = 23), although ∆SHS ≥ 5 was observed in 5 (56%) of nine patients with high MBDA scores.

CONCLUSIONS

We have shown, for the first time, that the MBDA score tracked disease activity in RA patients treated with rituximab and that change in MBDA score reflected the degree of treatment response.

摘要

背景

多生物标志物疾病活动(MBDA)评分已被验证为类风湿关节炎(RA)疾病活动的客观测量指标,并显示可跟踪几种疾病修饰抗风湿药物(DMARDs)的治疗反应。本研究的目的是评估 MBDA 评分跟踪利妥昔单抗治疗反应的能力。

方法

使用来自三个队列的 57 名接受利妥昔单抗 1000mg 和甲基强的松龙 100mg 治疗的 RA 患者的数据,于第 1 天和第 15 天。在基线和 6 个月时采集血清样本评估 MBDA 评分。计算基线值、6 个月值和从基线到 6 个月的变化(∆)之间的 MBDA 评分与以下指标之间的 Spearman 秩相关系数:使用红细胞沉降率(ESR)或高敏 C 反应蛋白(hsCRP)评估 28 个关节的疾病活动评分(DAS28),ESR,(hs)CRP,肿胀和压痛关节计数评估 28 个关节(SJC28,TJC28),患者一般健康的视觉模拟量表(VAS-GH),健康评估问卷(HAQ),以及 12 个月 Sharp/van der Heijde 评分(SHS)的放射学进展,以及六个骨转换标志物。此外,使用这些指标作为因变量,MBDA 评分作为自变量,进行多变量线性回归分析,并进行相关混杂因素的调整。在调整相关混杂因素后,评估∆MBDA 评分与 6 个月时的欧洲抗风湿病联盟(EULAR)反应之间的关联。

结果

基线时,MBDA 评分和 DAS28-ESR 的中位数分别为 54.0(IQR 44.3-70.0)和 6.3(IQR 5.4-7.1)。MBDA 评分与基线和 6 个月时的 DAS28-ESR、DAS28-hsCRP、ESR 和(hs)CRP 显著相关。∆MBDA 评分与这些指标的变化显著相关。∆MBDA 评分与 EULAR 良好或中度反应相关(调整后的 OR=0.89,95%CI=0.81-0.98,p=0.02)。基线 MBDA 评分和∆MBDA 评分均与∆SHS(n=11)或骨转换标志物的变化(n=23)无统计学显著相关性,尽管在 9 名高 MBDA 评分患者中有 5 名(56%)观察到∆SHS≥5。

结论

我们首次表明,MBDA 评分可跟踪接受利妥昔单抗治疗的 RA 患者的疾病活动,并且 MBDA 评分的变化反映了治疗反应的程度。

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