Spondyloarthritis & psoriatic arthritis

Serum calprotectin and complement factor C3 are superior biomarkers of inflammation in early psoriatic arthritis as compared with C-reactive protein

RMD OpenPublished Prospective cohort study

Authors' conclusion

C3 and calprotectin are elevated in early PsA and are responsive to treatment. These markers outperform CRP in obese and CRP-negative patients

Study context

Population
Adults with early, treatment-naïve psoriatic arthritis (PsA), compared with early rheumatoid arthritis (RA) and healthy controls
Participants
67 / 50 / 61
Exposure
Early PsA vs early RA vs healthy controls (HCs)
  • PsAn = 67
  • RAn = 50
  • HCn = 61reference
Outcome
Alternative biomarkers of inflammation (C3, S100A8/9, SAA) in early PsA
Follow-up
Baseline
Methodological detailsmulticentre
  • Multicentre

Main finding

As reported in the abstract

Median serum C3 and S100A8/9 levels
GroupValueS100A8/9 median
PsAmedian 1.38 g/L5.58 µg/mL

PsA

Valuemedian 1.38 g/L
S100A8/9 median5.58 µg/mL

Observational data: associations, not effects.

Further findings

C3 and S100A8/9 in 'C reactive protein (CRP)-negative' subgroup · baseline

C3 and S100A8/9 increased in PsA vs HC

Biomarkers in obese subgroup · baseline

CRP did not discriminate PsA, RA and HC
S100A8/9 significantly increased in PsA and RA vs HC
Serum amyloid A (SAA) and derived inflammatory ratios (neutrophil/monocyte, lymphocyte/monocyte) did not discriminate PsA, RA or HC

Change in C3 and S100A8/9 in PsA achieving low disease activity · 1 year

C3 and S100A8/9 decreased significantly

Diagnostic performance of composite C3×calprotectin vs CRP, obese subgroup

C3×calprotectin AUC, superior to CRP
0.836

Original publication

Serum calprotectin and complement factor C3 are superior biomarkers of inflammation in early psoriatic arthritis as compared with C-reactive protein. RMD Open. Published 23 September 2025. doi:10.1136/rmdopen-2025-006019

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