首页> 外文期刊>Annals of the Rheumatic Diseases: A Journal of Clinical Rheumatology and Connective Tissue Research >Association of joint space narrowing with impairment of physical function and work ability in patients with early rheumatoid arthritis: Protection beyond disease control by adalimumab plus methotrexate
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Association of joint space narrowing with impairment of physical function and work ability in patients with early rheumatoid arthritis: Protection beyond disease control by adalimumab plus methotrexate

机译:早期类风湿关节炎患者关节间隙变窄与身体功能和工作能力受损的关联:阿达木单抗联合甲氨蝶呤对疾病控制之外的保护

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Objectives: Tumour necrosis factor inhibition plus methotrexate is believed to inhibit radiographic progression independent of inflammation. This analysis assessed whether these protective effects are exerted on bone (joint erosion; JE) and/or cartilage (joint space narrowing; JSN), and what the independent effects of JE/JSN progression are on longer-term patient-reported outcomes. Methods: PREMIER was a 2-year, randomised, controlled trial of adalimumab plus methotrexate (ADA +MTX) versus the monotherapies. The impact of treatment on the relationships between time-averaged disease activity (TA-DAS28(CRP)) and changes in JE/JSN and associations of JE/JSN with the disability index of the health assessment questionnaire (HAQ-DI) at baseline and weeks 52 and 104 were assessed through non-parametric approaches of analysis of variance and quantile regression. JE/JSN association with employment status was evaluated at baseline and weeks 52 and 104 through logistic regression. Results: Increasing tertiles of TA-DAS28(CRP) were associated with JE and JSN progression in the monotherapy groups, a phenomenon largely absent in ADA+MTX-treated patients. Although JSN was not associated with HAQ-DI at baseline, it was at 52 and 104 weeks. In contrast, JE was not associated with HAQ-DI at any time point examined. Odds of being employed at baseline, 52 weeks and 104 weeks were significantly associated with lower JSN, but not JE, scores. Conclusions: ADA+MTX inhibited both JE and JSN progression independently of disease activity. JSN played a more prominent role in patient-reported outcomes than JE. Preventing the onset or worsening of JSN probably represents a critical aspect of effective disease management of early rheumatoid arthritis patients.
机译:目的:肿瘤坏死因子抑制加甲氨蝶呤被认为可以抑制放射成像进展,而与炎症无关。该分析评估了这些保护作用是否施加于骨骼(关节糜烂; JE)和/或软骨(关节间隙变窄; JSN),以及JE / JSN进展对患者长期报告的结局有何独立影响。方法:PREMIER是阿达木单抗加甲氨蝶呤(ADA + MTX)与单一疗法的2年随机对照试验。治疗对基线时的疾病平均活动时间(TA-DAS28(CRP))与JE / JSN变化以及JE / JSN与健康评估问卷的残疾指数(HAQ-DI)的关联之间的关系的影响第52周和第104周通过方差分析和分位数回归的非参数方法进行评估。通过逻辑回归在基线,第52和104周评估了JE / JSN与就业状况的关系。结果:在单药治疗组中,TA-DAS28(CRP)的三分位数增加与JE和JSN的进展有关,而在ADA + MTX治疗的患者中这种现象基本上不存在。尽管JSN在基线时与HAQ-DI不相关,但在52周和104周时。相反,在检查的任何时间点,JE均未与HAQ-DI相关。在基线,52周和104周时被雇用的几率与较低的JSN得分显着相关,而与JE得分无关。结论:ADA + MTX抑制JE和JSN进程独立于疾病活动。与JE相比,JSN在患者报告的结局中起着更加重要的作用。预防JSN的发作或恶化可能代表了早期类风湿关节炎患者有效疾病管理的关键方面。

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