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类风湿关节炎中间质性肺病和急性起病弥漫性间质性肺病的生物标志物

Biomarkers for interstitial lung disease and acute-onset diffuse interstitial lung disease in rheumatoid arthritis.

作者信息

Furukawa Hiroshi, Oka Shomi, Higuchi Takashi, Shimada Kota, Hashimoto Atsushi, Matsui Toshihiro, Tohma Shigeto

机构信息

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.

出版信息

Ther Adv Musculoskelet Dis. 2021 Jun 18;13:1759720X211022506. doi: 10.1177/1759720X211022506. eCollection 2021.

Abstract

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.

摘要

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。

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