Lupus & antiphospholipid syndrome

Association of Autoantibody Concentrations and Trajectories With Lupus Nephritis Histologic Features and Treatment Response

Arthritis RheumatolPublished Prospective cohort study

Authors' conclusion

Baseline levels of anti-C1q and anti-dsDNA may serve as noninvasive biomarkers of proliferative LN, and anti-C1q may predict complete response at the time of kidney biopsy.

Study context

Population
Patients with SLE undergoing diagnostic kidney biopsy based on proteinuria; 268 diagnosed with lupus nephritis (LN)268 with LN
Participants
279 patients
Exposure
Proliferative LN vs nonproliferative LN
  • Proliferative LNn = 160
  • Nonproliferative LNn = 108reference
Outcome
Association of circulating autoantibody concentrations (13 specificities by bead-based assay; anti-C1q by ELISA) with LN histologic class and treatment response
Methodological detailslongitudinal cohort, Accelerating Medicines Partnership LN cohort
  • Longitudinal cohort
  • Accelerating Medicines Partnership LN cohort

Main finding

As reported in the abstract

Autoantibody concentrations by LN class · baseline
  • Proliferative LN associated with higher anti-C1q, anti-chromatin, anti-dsDNA and anti-ribosomal P concentrations vs nonproliferative LN
  • Anti-C1q and anti-dsDNA independently associated with proliferative LN

Observational data: associations, not effects.

Further findings

OutcomeBaseline anti-C1qBaseline proteinuria
Prediction of complete response in proliferative LN · 12 months
AUC0.720.59
PP = 0.002P = 0.21

Autoantibody trajectories over 12 months

All autoantibody levels except anti-La/SSB decreased in proliferative, but not membranous, LN with complete response

Original publication

Association of Autoantibody Concentrations and Trajectories With Lupus Nephritis Histologic Features and Treatment Response. Arthritis Rheumatol. Published 9 August 2024. doi:10.1002/art.42941

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