Biomarkers for interstitial lung disease and acute-onset diffuse interstitial lung disease in rheumatoid arthritis.
Hiroshi FurukawaShomi OkaTakashi HiguchiKota ShimadaAtsushi HashimotoToshihiro MatsuiShigeto TohmaPublished in: Therapeutic advances in musculoskeletal disease (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 Pneumocystis 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.
Keyphrases
- interstitial lung disease
- rheumatoid arthritis
- idiopathic pulmonary fibrosis
- systemic sclerosis
- poor prognosis
- drug induced
- disease activity
- liver injury
- long non coding rna
- ankylosing spondylitis
- liver failure
- respiratory failure
- emergency department
- intensive care unit
- low grade
- healthcare
- gene expression
- acute respiratory distress syndrome
- small molecule
- genome wide
- high resolution
- electronic health record
- deep learning
- amino acid