Sjögren's disease & overlap diseases

Identification of distinct subgroups of Sjögren's disease by cluster analysis based on clinical and biological manifestations: data from the cross-sectional Paris-Saclay and the prospective Assessment of Systemic Signs and Evolution of Sjögren's Syndrome (ASSESS) cohorts

Lancet RheumatolPublished Cluster analysis of a cross-sectional cohort and a prospective cohort

Authors' conclusion

On the basis of symptoms and clinical and biological manifestations, we identified three distinct subgroups of patients with Sjögren's disease with different prognoses.

Study context

Population
Patients with SjD from two independent cohorts in France: cross-sectional Paris-Saclay (recruited 1999–2022) and prospective ASSESS (recruited 2006–2009)Paris-Saclay 534
Exposure
Clusters based on symptoms and clinical and biological manifestations
Outcome
Identification of distinct subgroups of SjD by cluster analysis using 26 variables (patient-reported symptoms, clinical and biological manifestations)
Methodological detailsunsupervised multiple correspondence analysis, hierarchical cluster analysis, external validation cohort, two independent cohorts
  • Unsupervised multiple correspondence analysis
  • Hierarchical cluster analysis
  • External validation cohort
  • Two independent cohorts

Main finding

As reported in the abstract

Clusters identified
In both cohorts, hierarchical cluster analysis revealed three distinct subgroups: BALS, HSA and LSAHS
3

Observational data: associations, not effects.

Further findings

OutcomeBALSHSAP value
ESSPRI score <5, BALS cluster (ASSESS) · month 60 vs inclusionP < 0.0001
Lymphoma incidence during follow-up (ASSESS)3%4%
Time to diagnosis after inclusion, median (IQR)70 months (42-104)— not stated in the abstract
Time to diagnosis after inclusion (IQR)— not stated in the abstract23 months (13-83)

— not stated in the abstract

  • ESSPRI score <5, BALS cluster (ASSESS): BALS, month 60 36%
  • ESSPRI score <5, BALS cluster (ASSESS): BALS, inclusion 49%
  • ESSPRI score <5, BALS cluster (ASSESS): of 186 patients; disease activity and symptom states worsened
  • Lymphoma incidence during follow-up (ASSESS): BALS of 186 patients; HSA of 158 patients

History of lymphoma (Paris-Saclay)

All patients with a history of lymphoma were in the BALS and HSA clusters

Comparison with symptom-only classification (Tarn and colleagues)

Clustering did not correlate with a previous classification based on symptoms only

Original publication

Identification of distinct subgroups of Sjögren's disease by cluster analysis based on clinical and biological manifestations: data from the cross-sectional Paris-Saclay and the prospective ASSESS cohorts. Lancet Rheumatol. Published 1 March 2024. doi:10.1016/s2665-9913(23)00340-5

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