Wolfe F, Caplan L, Michaud K
National Data Bank for Rheumatic Diseases, Arthritis Research Center Foundation, Wichita, KS 67214, USA.
Scand J Rheumatol. 2007 May-Jun;36(3):172-8. doi: 10.1080/03009740601153774.
Interstitial lung disease (ILD) is an important complication of rheumatoid arthritis (RA) or its treatment, and is associated with substantially increased mortality. Reports have suggested that infliximab with or without azathioprine might lead to rapidly progressive or fatal ILD. We used an RA data bank to assess the associations of treatments for RA and severe ILD.
ILD was identified in hospitalisations and death records in 100 of 17,598 RA patients and studied in relation to RA therapy with Cox regression analyses.
The incidence of hospitalisation for ILD (HILD) was 260 per 100,000 patient years. Among those hospitalised for ILD, 27.0% died. In multivariable models of current and past RA treatment, the only current treatment associated with HILD was prednisone: hazard ratio (HR) 2.5 [95% confidence interval (CI) 1.5-4.1]. Among past therapies, prednisone (HR 3.0, 95% CI 1.0-8.9), infliximab (HR 2.1, 95% CI 1.1-3.8), etanercept (HR 1.7, 95% CI 1.0-3.0), and cyclophosphamide (HR 3.7, 95% CI 0.9-15.5) were associated with HILD. Pre-existing lung problems were identified in 67% of HILD. Only one case of HILD in the 100 hospitalisations suggested a possible temporal relationship between infliximab and HILD.
Associations between RA treatment and HILD are confounded by the prescription of treatments for ILD such as prednisone, infliximab, etanercept, and cyclophosphamide. There is no clear pattern of causal association of treatment and ILD, and there is no clear evidence to support a causal relationship between infliximab, azathioprine, and HILD.
间质性肺病(ILD)是类风湿关节炎(RA)或其治疗的一种重要并发症,且与死亡率大幅增加相关。报告表明,使用或未使用硫唑嘌呤的英夫利昔单抗可能导致快速进展性或致命性ILD。我们利用一个RA数据库来评估RA治疗与严重ILD之间的关联。
在17598例RA患者中的100例患者的住院和死亡记录中确定了ILD,并通过Cox回归分析研究其与RA治疗的关系。
ILD住院(HILD)发生率为每100000患者年260例。在因ILD住院的患者中,27.0%死亡。在当前和既往RA治疗的多变量模型中,与HILD相关的唯一当前治疗药物是泼尼松:风险比(HR)为2.5 [95%置信区间(CI)1.5 - 4.1]。在既往治疗中,泼尼松(HR 3.0,95% CI 1.0 - 8.9)、英夫利昔单抗(HR 2.1,95% CI 1.1 - 3.8)、依那西普(HR 1.7,95% CI 1.0 - 3.0)和环磷酰胺(HR 3.7,95% CI 0.9 - 15.5)与HILD相关。67%的HILD患者存在既往肺部问题。在100例住院病例中,只有1例HILD提示英夫利昔单抗与HILD之间可能存在时间关系。
RA治疗与HILD之间的关联因泼尼松、英夫利昔单抗、依那西普和环磷酰胺等ILD治疗药物的处方而混淆。治疗与ILD之间没有明确的因果关联模式,也没有明确证据支持英夫利昔单抗、硫唑嘌呤与HILD之间存在因果关系。