Abstract

Adult-onset Still's disease (AOSD) is a systemic autoinflammatory disease in which danger-associated molecular patterns (DAMPs)-mediated inflammasome activation seems to be involved in the disease pathogenesis. Cold-inducible RNA-binding protein (CIRP) belongs to a family of cold-shock proteins that respond to cellular stress and has been identified as a DAMP that triggers the inflammatory response. The aim of this study is to investigate the clinical significance of serum CIRP levels in AOSD. Serum samples were obtained from 44 patients with active AOSD or 50 patients with rheumatoid arthritis (RA), 20 patients with systemic lupus erythematosus (SLE), and 15 healthy control patients (HCs). Serum levels of CIRP and IL-18 were determined using enzyme-linked immunosorbent assay. Results were compared among AOSD patients, RA patients, SLE patients and HCs. Results were also analyzed according to the clinical features of AOSD. Serum CIRP levels were significantly higher in AOSD patients compared with RA patients (median: 9.6 ng/mL, IQR [5.7-14.4] versus 3.2 ng/mL, IQR [1.9-3.8]; p < 0.001) and with HCs (2.8 ng/mL, [IQR; 1.4-4.9], p < 0.001). There was a significant positive correlation between serum CIRP levels and AOSD disease activity score (Pouchot's score r = 0.45, p = 0.003) as well as between AOSD-specific biomarkers ferritin and IL-18. However, there was no significant difference in the serum CIRP levels among AOSD patients with three different disease phenotypes. These results suggest that CIRP may play a significant role in the pathophysiology of AOSD and could be a potential biomarker for monitoring the disease activity of AOSD.

Highlights

  • Cold-inducible RNA-binding protein (CIRP) is a highly conserved 172-amino acid nuclear protein that belongs to the family of cold shock proteins [1]

  • The aim of this study is to investigate the clinical significance of serum CIRP levels in Adult-onset Still’s disease (AOSD)

  • Serum CIRP levels were significantly higher in AOSD patients compared with rheumatoid arthritis (RA) patients and with healthy control patients (HCs) (2.8 ng/mL, [IQR; 1.4–4.9], p < 0.001)

Read more

Summary

Introduction

Cold-inducible RNA-binding protein (CIRP) is a highly conserved 172-amino acid nuclear protein that belongs to the family of cold shock proteins [1]. Increased tissue and serum levels of CIRP have been reported in several inflammatory diseases [5]. ECIRP is a proinflammatory molecule that triggers inflammatory responses and organ damage, suggesting a role for CIRP in immune responses and inflammatory pathways [8]. CIRP is important as a damage-associated molecular protein (DAMPs) and is implicated in inflammatory diseases [9]. Cold-inducible RNA-binding protein (CIRP) belongs to a family of cold-shock proteins that respond to cellular stress and has been identified as a DAMP that triggers the inflammatory response.

Objectives
Methods
Results
Conclusion
Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call