Li Wanying, Sasso Eric H, van der Helm-van Mil Annette H M, Huizinga Tom W J
Statistics,
Medical and Scientific Affairs, Crescendo Bioscience, South San Francisco, USA and.
Rheumatology (Oxford). 2016 Feb;55(2):357-66. doi: 10.1093/rheumatology/kev341. Epub 2015 Sep 18.
To evaluate the multi-biomarker disease activity (MBDA) score as a predictor of radiographic progression and compare it with other risk factors among patients with established RA receiving non-biologic DMARDs.
For 163 patients with RA, we assessed 271 visits for MBDA score (scale of 1-100), clinical data and subsequent 1-year radiographic progression (change in Sharp-van der Heijde score [SHS]). Scatter plot and non-parametric quantile regression curves evaluated the relationship between the MBDA score and change in SHS. Changes in joint space narrowing and erosions were compared among MBDA categories with Wilcoxon rank-sum tests. The ability of the MBDA score to independently predict progression was determined by multivariate models and cross-classification of MBDA score with other risk factors. Generalized estimating equation methodology was used in model estimations to adjust for same-patient visits, always ≥1 year apart.
Patient characteristics included 67% female, 66%/67% RF(+)/anti-CCP(+); mean age 55 years, MBDA score 43 (moderate = 30-44); median disease duration 4.6 years, SHS 23. Radiographic progression was infrequent for low MBDA scores. Relative risk for progression increased continuously as the MBDA score increased, reaching 17.4 for change in SHS >5 with MBDA scores ≥60. Joint space narrowing and erosion progression were associated with MBDA score. MBDA score was associated with radiographic progression after adjustments for other risk factors. MBDA score significantly differentiated risk for progression when swollen joint count, CRP or DAS28-CRP was low, and among seropositive patients.
MBDA score enhanced the ability of conventional risk factors to predict radiographic progression in patients with established RA receiving non-biologic DMARDs.
评估多生物标志物疾病活动(MBDA)评分作为影像学进展预测指标的价值,并将其与接受非生物改善病情抗风湿药物(DMARDs)治疗的类风湿关节炎(RA)患者的其他危险因素进行比较。
对163例RA患者进行了271次随访,评估其MBDA评分(1 - 100分)、临床数据及随后1年的影像学进展(Sharp-van der Heijde评分[SHS]变化)。散点图和非参数分位数回归曲线评估了MBDA评分与SHS变化之间的关系。采用Wilcoxon秩和检验比较不同MBDA类别之间关节间隙狭窄和骨侵蚀的变化。通过多变量模型以及MBDA评分与其他危险因素的交叉分类来确定MBDA评分独立预测进展的能力。模型估计采用广义估计方程方法,以校正间隔至少1年的同一患者随访数据。
患者特征包括67%为女性,66%/67%类风湿因子(RF)阳性/抗环瓜氨酸肽抗体(anti-CCP)阳性;平均年龄55岁;MBDA评分为43(中度=30 - 44);疾病持续时间中位数为4.6年,SHS为23。MBDA评分低时影像学进展不常见。随着MBDA评分升高,进展的相对风险持续增加,MBDA评分≥60时SHS变化>5的相对风险达到17.4。关节间隙狭窄和骨侵蚀进展与MBDA评分相关。校正其他危险因素后,MBDA评分与影像学进展相关。当肿胀关节计数、C反应蛋白(CRP)或28关节疾病活动评分(DAS28-CRP)较低时,以及在血清学阳性患者中,MBDA评分显著区分进展风险。
MBDA评分增强了传统危险因素对接受非生物DMARDs治疗的已确诊RA患者影像学进展的预测能力。