Department of Rheumatology and Clinical Immunology, Saitama Medical Center, Saitama Medical University, Kawagoe, Japan.
Clin Exp Rheumatol. 2010 May-Jun;28(3):365-72. Epub 2010 Jun 23.
We conducted a two-year prospective study to identify possible factors associated with normalisation of physical function by infliximab treatment in 125 patients with rheumatoid arthritis (RA).
RA patients who had been scheduled to receive infliximab at 3 mg/kg were registered and prospectively examined for disease activity, joint damage, and physical function for 102 weeks using the Disease Activity Score of 28 Joints (DAS-28) using C-reactive protein, van der Heijde-modified Sharp score (vdH-Sharp score) of hand and foot x-ray, and Health Assessment Questionnaire Disability Index (HAQ-DI). Normal physical function and clinical remission were defined as a HAQ-DI of 0.5 or less, and DAS28 (CRP) <2.6, respectively.
Forty-two of 125 patients (42%) achieved normal physical function at 102 weeks. The percentage of normal physical function at 102 weeks was significantly higher in the patients achieving clinical remission at 102 weeks (60%) than in those without (16%). In the patients with clinical remission at 102 weeks, less structural damage at baseline was correlated with a higher rate of normal physical function, suggesting the critical importance of joint destruction prior to infliximab therapy, in addition to clinical response. Logistic regression analysis further identified HAQ-DI, serum MMP-3 level, vdH-Sharp score, and methotrexate (MTX) dose as baseline factors contributing to normal physical function with 2-year infliximab treatment.
Treatment with anti-TNF biologics in combination with MTX may achieve the normalisation of physical function in patients with established RA. Critical factors contributing to the normalisation of function were tight control of disease activity and less joint damage.
我们进行了一项为期两年的前瞻性研究,以确定 125 例类风湿关节炎(RA)患者接受英夫利昔单抗治疗后,身体功能正常化可能相关的因素。
登记了计划接受英夫利昔单抗 3mg/kg 治疗的 RA 患者,并前瞻性地检查了 102 周的疾病活动度、关节损伤和身体功能,使用 C 反应蛋白的 28 关节疾病活动评分(DAS-28)、手部和足部 X 射线的 van der Heijde 改良 Sharp 评分(vdH-Sharp 评分)和健康评估问卷残疾指数(HAQ-DI)。正常的身体功能和临床缓解定义为 HAQ-DI 为 0.5 或更低,DAS28(CRP)<2.6。
125 例患者中有 42 例(42%)在 102 周时达到正常的身体功能。在 102 周时达到临床缓解的患者中,达到正常身体功能的比例(60%)显著高于未达到临床缓解的患者(16%)。在 102 周时达到临床缓解的患者中,基线时较少的结构损伤与更高的正常身体功能率相关,这表明在接受英夫利昔单抗治疗之前,关节破坏的严重程度除了临床反应外,对身体功能的正常化至关重要。逻辑回归分析进一步确定了 HAQ-DI、血清 MMP-3 水平、vdH-Sharp 评分和甲氨蝶呤(MTX)剂量作为接受英夫利昔单抗治疗 2 年后正常身体功能的基线因素。
抗 TNF 生物制剂联合 MTX 治疗可能使已确诊的 RA 患者的身体功能正常化。对功能正常化有贡献的关键因素是疾病活动的严格控制和较少的关节损伤。