Infliximab use and cervical spine deformity in patients with rheumatoid arthritis.

IF 4.7 2区 医学 Q1 RHEUMATOLOGY RMD Open Pub Date : 2025-03-18 DOI:10.1136/rmdopen-2024-005237
Anna Baukje Lebouille-Veldman, Tom W J Huizinga, Rania A Mekary, Carmen L A Vleggeert-Lankamp
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Abstract

Objective: Over the past decades, the incidence of surgery for rheumatoid arthritis (RA)-associated cervical spine deformity decreased. Infliximab has been observed as a protective treatment for joint damage in hands and feet; yet, the protective association between infliximab and the cervical spine has been uncertain.

Methods: Duration of infliximab use during 10 years of follow-up was evaluated in patients with new-onset RA (case control study using data from the BeSt Trial). Missing values on the exposure were imputed using last observation carried forward. Lateral X-rays at 5-year and 10-year follow-ups were assessed for atlantoaxial subluxation (AAS) and subaxial subluxation (SAS). Multiple logistic regression models adjusted for age, gender, baseline Disease Activity Score (DAS44), ACPA-positivity and rheumatoid factor-positivity were used to estimate ORs and their 95% CIs. Mediation analysis was performed to evaluate whether a potential association was mediated via mean DAS44.

Results: Cervical deformity (AAS and/or SAS>2 mm) was observed in 108 (40%) of 272 patients. There was an 11% reduction in odds for cervical spine deformity (OR: 0.89, 95% CI: 0.81 to 0.98; p=0.02) for every 1-year increase in duration of infliximab use. Mediation analysis could not reveal an influence of DAS44 on the association between infliximab use and cervical spine outcomes.

Conclusions: There was evidence of a beneficial association between longer duration of use of infliximab and cervical spine deformity after 10 years follow-up. Thus, it is important to balance the favourable effects of infliximab use for the joints and possibly the cervical spine with the potential adverse events of this medication when used continuously.

Trial registration number: Netherlands Trial Register Number: NTR262.

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类风湿性关节炎患者使用英夫利西单抗和颈椎畸形。
目的:在过去的几十年里,类风湿性关节炎(RA)相关颈椎畸形的手术发生率有所下降。英夫利昔单抗已被观察为手和脚关节损伤的保护性治疗;然而,英夫利昔单抗与颈椎之间的保护关系尚不确定。方法:评估新发RA患者在10年随访期间英夫利昔单抗的使用时间(病例对照研究,使用BeSt试验的数据)。利用结转的最后一次观测值来推算暴露上的缺失值。在5年和10年随访中评估侧位x线片对寰枢半脱位(AAS)和亚轴半脱位(SAS)的影响。采用调整了年龄、性别、基线疾病活动评分(DAS44)、acpa阳性和类风湿因子阳性的多重logistic回归模型来估计or及其95% ci。进行中介分析以评估是否通过平均DAS44介导了潜在的关联。结果:272例患者中有108例(40%)出现颈椎畸形(AAS和/或SAS bbb2.0 mm)。颈椎畸形的几率降低了11% (OR: 0.89, 95% CI: 0.81 ~ 0.98;P =0.02),英夫利昔单抗使用时间每增加1年。中介分析不能揭示DAS44对英夫利昔单抗使用与颈椎结局之间的关联的影响。结论:经过10年的随访,有证据表明英夫利昔单抗使用时间较长与颈椎畸形之间存在有益的关联。因此,平衡英夫利昔单抗对关节和颈椎的有利作用与持续使用该药物的潜在不良事件是很重要的。试验注册号:荷兰试验注册号:NTR262。
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来源期刊
RMD Open
RMD Open RHEUMATOLOGY-
CiteScore
7.30
自引率
6.50%
发文量
205
审稿时长
14 weeks
期刊介绍: RMD Open publishes high quality peer-reviewed original research covering the full spectrum of musculoskeletal disorders, rheumatism and connective tissue diseases, including osteoporosis, spine and rehabilitation. Clinical and epidemiological research, basic and translational medicine, interesting clinical cases, and smaller studies that add to the literature are all considered.
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