Nail-bed infarctions as a paradoxical effect of abatacept in rheumatoid arthritis

S. M. A. Galil, Mohamed Fahmi
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Abstract

Objective: Evaluating a group of Rheumatoid Arthritis (RA) patients under abatacept therapy regarding the risk of developing vasculitis. Methods: An exploratory study was conducted on RA patients with ongoing combined methotrexate/ abatacept therapy and reporting a case who developed small-vessel vasculitis. Follow-up visits with thorough clinical examination and routine laboratory investigations were done every 3-6 months. Disease activity was assessed by the Clinical Disease Activity Index (CDAI). Functional assessment was done by Health Assessment Questionnaire (HAQ) score. Results: Sixteen biologic-naive female patients with newly diagnosed moderate-to-severe RA under abatacept therapy (mean age, 44 ± 10.86 years) were enrolled in this study. The mean disease duration was 4.63 ± 2.20, mean duration of methotrexate/abatacept therapy was 22.75 ± 9.40 months. All over the follow-up periods, patients were clinically improved with low disease activity score and within normal laboratory investigations apart from rising titers of Sedimentation Rate (ESR) and C-Reactive Protein (CRP). One patient was presented by nail-bed infarctions after 15 months follow-up of abatacept therapy. Abatacept–induced small-vessel vasculitis was the most likely diagnosis. The remaining 15 patients still clinically free of any manifestations suggesting vasculitis. Conclusion: Abatacept can induce vasculitis in RA patients having risk factors for RV. Combination therapy of methotrexate/abatacept may be a delaying or inhibiting factor in the appearance of RV manifestations. Persistently elevated acute phase reactants despite clinical and laboratory improvement on early aggressive treatment of RA is an alarm for a possibly imminent vasculitis.
甲床梗死作为阿巴肽在类风湿关节炎中的矛盾作用
目的:评价类风湿关节炎(RA)患者接受阿巴接受治疗后发生血管炎的风险。方法:对正在进行甲氨蝶呤/阿巴接受联合治疗的RA患者进行探索性研究,并报告1例发生小血管炎的病例。每3-6个月随访一次,进行全面临床检查和常规实验室检查。采用临床疾病活动性指数(CDAI)评估疾病活动性。功能评估采用健康评估问卷(HAQ)评分。结果:16例接受abataccept治疗的新诊断的中重度RA女性患者(平均年龄44±10.86岁)被纳入本研究。平均病程为4.63±2.20个月,甲氨蝶呤/阿巴接受治疗平均病程为22.75±9.40个月。在整个随访期间,除了沉降率(ESR)和c反应蛋白(CRP)滴度上升外,患者的疾病活动性评分较低,实验室检查正常。1例患者在接受阿巴接受治疗15个月后出现甲床梗死。abataccept诱导的小血管炎是最有可能的诊断。其余15例患者临床无血管炎表现。结论:阿巴那肽可诱导具有RV危险因素的RA患者发生血管炎。甲氨蝶呤/阿巴接受联合治疗可能是延迟或抑制RV表现的因素。尽管临床和实验室对RA的早期积极治疗有所改善,但急性期反应物持续升高是可能即将发生血管炎的警报。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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