Juge Pierre-Antoine, Lee Joyce S, Lau Jessica, Kawano-Dourado Leticia, Rojas Serrano Jorge, Sebastiani Marco, Koduri Gouri, Matteson Eric, Bonfiglioli Karina, Sawamura Marcio, Kairalla Ronaldo, Cavagna Lorenzo, Bozzalla Cassione Emanuele, Manfredi Andreina, Mejia Mayra, Rodríguez-Henriquez Pedro, González-Pérez Montserrat I, Falfán-Valencia Ramcés, Buendia-Roldán Ivette, Pérez-Rubio Gloria, Ebstein Esther, Gazal Steven, Borie Raphaël, Ottaviani Sébastien, Kannengiesser Caroline, Wallaert Benoît, Uzunhan Yurdagul, Nunes Hilario, Valeyre Dominique, Saidenberg-Kermanac'h Nathalie, Boissier Marie-Christophe, Wemeau-Stervinou Lidwine, Flipo René-Marc, Marchand-Adam Sylvain, Richette Pascal, Allanore Yannick, Dromer Claire, Truchetet Marie-Elise, Richez Christophe, Schaeverbeke Thierry, Lioté Huguette, Thabut Gabriel, Deane Kevin D, Solomon Joshua J, Doyle Tracy, Ryu Jay H, Rosas Ivan, Holers V Michael, Boileau Catherine, Debray Marie-Pierre, Porcher Raphaël, Schwartz David A, Vassallo Robert, Crestani Bruno, Dieudé Philippe
Dept of Rheumatology, DMU Locomotion, INSERM UMR1152, Hôpital Bichat-Claude Bernard, APHP, Université de Paris, Paris, France.
These authors contributed equally.
Eur Respir J. 2021 Feb 11;57(2). doi: 10.1183/13993003.00337-2020. Print 2021 Feb.
Methotrexate (MTX) is a key anchor drug for rheumatoid arthritis (RA) management. Fibrotic interstitial lung disease (ILD) is a common complication of RA. Whether MTX exposure increases the risk of ILD in patients with RA is disputed. We aimed to evaluate the association of prior MTX use with development of RA-ILD.
Through a case-control study design with discovery and international replication samples, we examined the association of MTX exposure with ILD in 410 patients with chronic fibrotic ILD associated with RA (RA-ILD) and 673 patients with RA without ILD. Estimates were pooled over the different samples using meta-analysis techniques.
Analysis of the discovery sample revealed an inverse relationship between MTX exposure and RA-ILD (adjusted OR 0.46, 95% CI 0.24-0.90; p=0.022), which was confirmed in the replication samples (pooled adjusted OR 0.39, 95% CI 0.19-0.79; p=0.009). The combined estimate using both the derivation and validation samples revealed an adjusted OR of 0.43 (95% CI 0.26-0.69; p=0.0006). MTX ever-users were less frequent among patients with RA-ILD compared to those without ILD, irrespective of chest high-resolution computed tomography pattern. In patients with RA-ILD, ILD detection was significantly delayed in MTX ever-users compared to never-users (11.4±10.4 years and 4.0±7.4 years, respectively; p<0.001).
Our results suggest that MTX use is not associated with an increased risk of RA-ILD in patients with RA, and that ILD was detected later in MTX-treated patients.
甲氨蝶呤(MTX)是类风湿关节炎(RA)治疗的关键基础药物。纤维化间质性肺病(ILD)是RA的常见并发症。MTX暴露是否会增加RA患者发生ILD的风险存在争议。我们旨在评估既往使用MTX与RA-ILD发生之间的关联。
通过一项包含发现样本和国际重复样本的病例对照研究设计,我们在410例患有与RA相关的慢性纤维化ILD(RA-ILD)的患者和673例无ILD的RA患者中,研究了MTX暴露与ILD之间的关联。使用荟萃分析技术对不同样本的估计值进行汇总。
对发现样本的分析显示MTX暴露与RA-ILD之间存在负相关(校正比值比0.46,95%可信区间0.24-0.90;p=0.022),这在重复样本中得到证实(汇总校正比值比0.39,95%可信区间0.19-0.79;p=0.009)。使用推导样本和验证样本的合并估计值显示校正比值比为0.43(95%可信区间0.26-0.69;p=0.0006)。与无ILD的患者相比,RA-ILD患者中曾经使用MTX的频率较低,无论胸部高分辨率计算机断层扫描模式如何。在RA-ILD患者中,曾经使用MTX的患者与从未使用过MTX的患者相比,ILD检测明显延迟(分别为11.4±10.4年和4.0±7.4年;p<0.001)。
我们的结果表明,MTX的使用与RA患者发生RA-ILD的风险增加无关,并且在接受MTX治疗的患者中ILD检测较晚。