Autoinflammatory & rare systemic diseases

IgG4 surge and relapse: determining the predictive threshold for IgG4 rising kinetics in IgG4-related disease

Rheumatology (Oxford)Published Cohort study

Authors' conclusion

The IgG4 surge defined as an IgG4-Ratio >1.6 (indicating a >60% increase in IgG4 levels between consecutive measurements taken at median 3-month intervals) predicts relapse in the majority of seropositive IgG4-RD patients. Intensified treatment in patients with IgG4 surge can reduce recurrence risk.

Study context

Population
Patients with IgG4-related disease (IgG4-RD) with >6 months of follow-up and ≥3 IgG4 measurements, Chinese PLA General Hospital, February 2016 to May 2023median follow-up 33 months
Participants
155 patients
Exposure
IgG4 dynamics (IgG4-Ratio thresholds) vs single-timepoint IgG4 level for predicting relapse; intensified treatment after IgG4 surge
Outcome
Relapse predicted by IgG4-Ratio (sequential visit-to-visit fold-change) and single-timepoint IgG4 level
Methodological detailssingle-centre, time-dependent Cox regression, restricted cubic splines
  • Single-centre
  • Time-dependent Cox regression
  • Restricted cubic splines

Main finding

As reported in the abstract

Prediction of relapse
IgG4-Ratio thresholds >1.1-1.3 and >1.6-1.8 significantly predicted relapse
P < 0.05
Restricted cubic splines (RCS) nonlinear dose-response relationship
P = 0.008
Optimal threshold to predict relapse: IgG4-Ratio
>1.6

Observational data: associations, not effects.

Further findings

Relapse risk with intensified treatment in patients with IgG4-Ratio >1.6 (n=45)

HR (95% CI)P value
Intensified treatmentRelapse risk reduced by 68.3%0.317 (0.102–0.988)P = 0.048

IgG4 normalization among patients with baseline IgG4 positivity (149)

IgG4 normalized
63.8% (95/149)
IgG4 re-positivity among those normalized
61.1% (58/95)

Original publication

IgG4 surge and relapse: determining the predictive threshold for IgG4 rising kinetics in IgG4-related disease. Rheumatology (Oxford). Published 27 February 2026. doi:10.1093/rheumatology/keag034

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