Landewé Robert, van der Heijde Désirée, Klareskog Lars, van Vollenhoven Ronald, Fatenejad Saeed
University Hospital Maastricht, Maastricht, The Netherlands.
Arthritis Rheum. 2006 Oct;54(10):3119-25. doi: 10.1002/art.22143.
To determine the relationship between disease activity and radiographic progression of joint destruction in patients with rheumatoid arthritis (RA) treated with methotrexate (MTX), those treated with etanercept, and those treated with the combination of MTX plus etanercept.
Baseline, 12-month, and 24-month data from the Trial of Etanercept and Methotrexate with Radiographic and Patient Outcomes database were analyzed. The dependent variable was the 1-year change in the modified Sharp/van der Heijde score (Sharp score); therefore, 2 interval changes per patient were available. Interval change in the Sharp score was modeled by time (years), treatment, disease activity, and the interaction (disease activity x treatment). Disease activity was reflected by the time-averaged Disease Activity Score (taDAS) and the time-averaged C-reactive protein (taCRP) level, which were calculated per 1-year interval. Generalized mixed linear modeling (GMLM) was used to adjust for within-patient correlation.
GMLM confirmed a significant interaction between treatment and the taCRP level and taDAS with respect to the change in Sharp score (P = 0.012 and P = 0.03, respectively). In patients treated with MTX alone, radiographic progression increased with an increasing taCRP level or taDAS, although progression rates were low in patients whose disease was in remission and in those with low-to-moderate disease activity. This relationship was less clear in patients treated with etanercept and was absent in those who received combination therapy.
Combination therapy with MTX plus etanercept uncouples the classic relationship between disease activity and radiographic progression in patients with RA.
确定接受甲氨蝶呤(MTX)治疗、接受依那西普治疗以及接受MTX加依那西普联合治疗的类风湿关节炎(RA)患者的疾病活动度与关节破坏影像学进展之间的关系。
分析了来自依那西普和甲氨蝶呤联合影像学及患者预后试验数据库的基线、12个月和24个月的数据。因变量是改良夏普/范德海伊德评分(夏普评分)的1年变化;因此,每位患者有2个间隔变化数据。夏普评分的间隔变化通过时间(年)、治疗、疾病活动度以及交互作用(疾病活动度×治疗)进行建模。疾病活动度通过每1年间隔计算的时间平均疾病活动评分(taDAS)和时间平均C反应蛋白(taCRP)水平来反映。采用广义混合线性模型(GMLM)来调整患者内相关性。
GMLM证实治疗与taCRP水平及taDAS在夏普评分变化方面存在显著交互作用(分别为P = 0.012和P = 0.03)。在仅接受MTX治疗的患者中,影像学进展随taCRP水平或taDAS升高而增加,尽管疾病缓解患者以及疾病活动度低至中度的患者进展率较低。这种关系在接受依那西普治疗的患者中不太明显,而在接受联合治疗的患者中不存在。
MTX加依那西普联合治疗打破了RA患者疾病活动度与影像学进展之间的经典关系。