Furukawa Hiroshi, Oka Shomi, Higuchi Takashi, Shimada Kota, Hashimoto Atsushi, Matsui Toshihiro, Tohma Shigeto
Department of Rheumatology, National Hospital Organization Tokyo National Hospital, 3-1-1 Takeoka, Kiyose 204-8585, Japan.
Department of Rheumatology, National Hospital Organization Tokyo National Hospital, Kiyose, Japan.
Ther Adv Musculoskelet Dis. 2021 Jun 18;13:1759720X211022506. doi: 10.1177/1759720X211022506. eCollection 2021.
Interstitial lung disease (ILD) is frequently a complication of rheumatoid arthritis (RA) as an extra-articular manifestation which has a poor prognosis. Acute-onset diffuse ILD (AoDILD) occasionally occurs in RA and includes acute exacerbation of ILD, drug-induced ILD, and pneumonia. AoDILD also confers a poor prognosis in RA. Previously-established biomarkers for ILD include Krebs von den lungen-6 and surfactant protein-D originally defined in patients with idiopathic pulmonary fibrosis; the sensitivity of these markers for RA-associated ILD (RA-ILD) is low. Although many studies on ILD markers have been performed in idiopathic pulmonary fibrosis, only a few validation studies in RA-ILD or AoDILD have been reported. Biomarkers for RA-ILD and AoDILD are thus still required. Recently, genomic, cytokine, antibody, and metabolomic profiles of RA-ILD or AoDILD have been investigated with the aim of improving biomarkers. In this review, we summarize current preliminary data on these potential biomarkers for RA-ILD or AoDILD. The development of biomarkers on RA-ILD has only just begun. When validated, such candidate biomarkers will provide valuable information on pathogenesis, prognosis, and drug responses in RA-ILD in future.
间质性肺疾病(ILD)常作为类风湿关节炎(RA)的关节外表现而出现,预后较差。急性起病的弥漫性ILD(AoDILD)偶尔会在RA中发生,包括ILD急性加重、药物性ILD和肺炎。AoDILD在RA中预后也较差。先前确立的ILD生物标志物包括最初在特发性肺纤维化患者中定义的克雷伯氏肺6和表面活性蛋白-D;这些标志物对RA相关ILD(RA-ILD)的敏感性较低。尽管针对ILD标志物在特发性肺纤维化方面已开展了许多研究,但在RA-ILD或AoDILD方面仅有少数验证性研究被报道。因此,仍需要RA-ILD和AoDILD的生物标志物。最近,为了改进生物标志物,对RA-ILD或AoDILD的基因组、细胞因子、抗体和代谢组学特征进行了研究。在这篇综述中,我们总结了关于这些RA-ILD或AoDILD潜在生物标志物的当前初步数据。RA-ILD生物标志物的开发才刚刚起步。一旦得到验证,此类候选生物标志物将在未来为RA-ILD的发病机制、预后和药物反应提供有价值的信息。