Autoinflammatory & rare systemic diseases

Clinical significance of non-infectious procalcitonin elevation in Still’s disease: a predictor of macrophage activation syndrome

Rheumatology (Oxford)Published Retrospective cohort study

Authors' conclusion

Elevated PCT levels may serve as an independent predictor of MAS in SD.

Study context

Population
Patients with Still's disease without infection with available procalcitonin (PCT) datapatients with SD
Participants
110 patients
Exposure
SD with non-infectious PCT ≥ 0.5 vs PCT < 0.5 ng/ml (baseline and maximum values); controls with bloodstream infection and matched healthy controls (HCs)
  • PCT ≥ 0.5n = 35
  • PCT < 0.5n = 75reference
  • PCTmax ≥ 0.5n = 47
  • PCTmax < 0.5n = 63reference
Outcome
Relationship between non-infectious PCT elevation and clinical features of SD, incl. MAS
Methodological detailsPCT cut-off 0.5 ng/ml, univariate and multivariate analysis
  • PCT cut-off 0.5 ng/ml
  • Univariate and multivariate analysis

Main finding

As reported in the abstract

MAS risk by PCT elevation

Macrophage activation syndrome (MAS) risk, PCT ≥ 0.5 vs PCT < 0.5, univariate

6.4-fold

MAS risk, PCTmax ≥ 0.5 vs PCTmax < 0.5, univariate

7.6-fold

MAS risk, PCT ≥ 0.5 vs PCT < 0.5, multivariate

4.3-fold

MAS risk, PCTmax ≥ 0.5 vs PCTmax < 0.5, multivariate

5.4-fold

Observational data: associations, not effects.

Further findings

PCT levels vs controls

PCT significantly higher in SD than HCs; nearly as elevated in MAS cases as in infection

Clinical features associated with elevated PCT

MAS frequency, higher mPouchot scores and increased bDMARD use, particularly anakinra, associated with elevated PCT

Original publication

Clinical significance of non-infectious procalcitonin elevation in Still’s disease: a predictor of macrophage activation syndrome. Rheumatology (Oxford). Published 29 October 2025. doi:10.1093/rheumatology/keaf575

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