Pediatric rheumatology

Anti-mitochondrial antibodies as markers of disease activity in childhood-onset systemic lupus erythematosus: a longitudinal cohort study

Rheumatology (Oxford)Published Prospective longitudinal cohort study

Authors' conclusion

AMA-IgG emerges as a promising biomarker of disease activity in cSLE, and its increase is in alignment with elevated IFNα2 expression.

Study context

Population
Patients with childhood-onset SLE (cSLE)cSLE, sera at 2 timepoints (TPs)
Participants
29 patients
Exposure
Active disease vs clinically quiescent disease
Outcome
Anti-mitochondrial antibodies (AMA) and disease activity
Methodological detailstwo timepoints (active vs quiescent disease), AMA IgG, IgM and IgA binding to human mitochondria assessed by flow cytometry; IFNα2 by single-molecule array
  • Two timepoints (active vs quiescent disease)
  • AMA IgG, IgM and IgA binding to human mitochondria assessed by flow cytometry; IFNα2 by single-molecule array

Main finding

As reported in the abstract

AMA-IgG decreased between TP-1 and TP-2
P = 0.0426
AMA-IgG correlation with SLEDAI at TP-1
ρ = 0.41, P = 0.026
AMA-IgG correlation with anti-dsDNA at TP-1
ρ = 0.66, P = 0.0001
AMA-IgM oscillated according to disease activity
P = 0.0065
AMA-IgG correlation with IFNα2 during active disease
ρ = 0.729, P < 0.0001
AMA-IgM correlation with IFNα2 during active disease
ρ = 0.631, P = 0.001

Observational data: associations, not effects.

Further findings

Disease activity and treatment at each timepoint

Median prednisone dose TP-1 0.43 mg/kg/day · TP-2 0.14 mg/kg/day

Disease activity and treatment at each timepoint — Median age at diagnosis
14.9 ± 3.6 years
Disease activity and treatment at each timepoint — Median interval between TP-1 and TP-2
6 ± 3.7 months

Original publication

Anti-mitochondrial antibodies as markers of disease activity in childhood-onset systemic lupus erythematosus: a longitudinal cohort study. Rheumatology (Oxford). Published 23 May 2025. doi:10.1093/rheumatology/keaf275

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