University Hospital of Bern, Bern, Switzerland.
AbbVie, North Chicago, Illinois.
Arthritis Care Res (Hoboken). 2018 Jun;70(6):861-868. doi: 10.1002/acr.23427. Epub 2018 Apr 25.
To study low blood hemoglobin concentrations as a predictor of radiographic damage progression in patients with rheumatoid arthritis (RA).
Post hoc analyses were performed in patients from the PREMIER trial with early RA undergoing 2 years of adalimumab (ADA), methotrexate (MTX), or ADA + MTX combination therapy. Low disease activity was defined as a score <3.2 on the 28-joint Disease Activity Score using the C-reactive protein level (DAS28-CRP), and clinical response by the American College of Rheumatology criteria for 20% improvement at week 24. Baseline or mean hemoglobin concentrations over time, or anemia as defined using sex-specific World Health Organization criteria, were analyzed in mixed-effects models for longitudinal data in men and women as predictors of progressive joint damage, as measured by the modified total Sharp/van der Heijde score (ΔSHS). Data were adjusted for treatment and other patient characteristics, including the DAS28-CRP.
Baseline hemoglobin was inversely associated with ΔSHS in adjusted analyses (P < 0.05 for both sexes). Baseline anemia predicted greater ΔSHS in MTX-treated patients over 104 weeks, and in ADA- and combination-treated patients over 26 weeks. Lower hemoglobin concentrations over time, as well as time with anemia, were associated with greater damage progression (P < 0.001). The effect of low hemoglobin concentrations on joint damage progression remained significant, even in patients achieving low disease activity.
Low hemoglobin is a DAS28-CRP-independent predictor of radiographic joint damage progression in MTX-treated patients with early RA. This effect decreases over time in ADA- and combination-treated patients, and in clinical responders irrespective of treatment modality.
研究低血红蛋白浓度作为类风湿关节炎(RA)患者放射学损伤进展的预测指标。
对接受阿达木单抗(ADA)、甲氨蝶呤(MTX)或 ADA+MTX 联合治疗的早期 RA 患者进行 PREMIER 试验的事后分析。低疾病活动度定义为使用 C 反应蛋白水平(DAS28-CRP)的 28 个关节疾病活动度评分(DAS28)<3.2,临床反应定义为美国风湿病学会 24 周时 20%的改善标准。对男性和女性的纵向数据进行混合效应模型分析,以评估基线或随时间变化的平均血红蛋白浓度或使用特定性别的世界卫生组织贫血标准定义的贫血作为进行性关节损伤的预测指标,通过改良总 Sharp/van der Heijde 评分(ΔSHS)进行测量。数据调整了治疗和其他患者特征,包括 DAS28-CRP。
在调整后的分析中,基线血红蛋白与ΔSHS 呈负相关(男女均 P<0.05)。基线贫血预测 MTX 治疗患者在 104 周内、ADA 和联合治疗患者在 26 周内的ΔSHS 更大。随时间变化的较低血红蛋白浓度以及贫血时间与更大的损伤进展相关(P<0.001)。即使在达到低疾病活动度的患者中,低血红蛋白浓度对关节损伤进展的影响仍然显著。
低血红蛋白是 MTX 治疗早期 RA 患者放射学关节损伤进展的 DAS28-CRP 独立预测指标。这种影响在 ADA 和联合治疗患者以及无论治疗方式如何的临床反应者中随时间逐渐降低。