Rheumatoid arthritis

Validation of a Genetic Risk Score Combined With Clinical Variables for Predicting Pulmonary Fibrosis in Early Rheumatoid Arthritis

Arthritis Care Res (Hoboken)Published Prognostic model external validation study

Performance · Discrimination of RA-PFResult — go to the resultOdds ratio 2.6 95% CI 1.6–4.5

Authors' conclusion

This study provides external validation of the Veterans Affairs Rheumatoid Arthritis Registry interstitial lung disease GRS (VARA-ILD-GRS) and the VARA-ILD-CRS in an RA cohort, demonstrating their generalizability and effectiveness in identifying individuals at high risk for RA-ILD.

Study context

Population
Inception cohort of patients diagnosed with early rheumatoid arthritis (RA), northern Sweden, 1996–20161,115 with complete data
Participants
1,118 participants
Comparison
Combined risk score (CRS) vs genetic risk score (GRS) alone for predicting RA-associated pulmonary fibrosis (PF)
Outcome
Prediction of RA-associated PF development (GRS and CRS performance)
Methodological detailsinception cohort, logistic regression, AUC assessment
  • Inception cohort
  • Logistic regression
  • AUC assessment

Performance

Discrimination of RA-PF

Odds ratio

2.6

95% CI 1.6–4.5

By group

CRS

0.75

AUC

GRS

0.62

AUC

GRS
OR 2.6 (95% CI 1.6–4.5)

As reported in the abstract

Further findings

RA-PF incidence among patients with complete data

Patients with complete data diagnosed with PF
60 (5.6%)
  • 1,115 patients with complete data

Factors associated with PF

PF significantly associated with age, RF positivity, disease activity, and MUC5B (rs35705950) and FAM13A (rs2609255) single-nucleotide polymorphisms (SNPs)

Original publication

Validation of a Genetic Risk Score Combined With Clinical Variables for Predicting Pulmonary Fibrosis in Early Rheumatoid Arthritis. Arthritis Care Res (Hoboken). Published 1 February 2026. doi:10.1002/acr.25696

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