Table 3

Associations between clinical manifestations and SLE B cell PRS (n=1248)

OR* (95% CI)P value
ACR criteria23
 ACR 1: malar rash0.97 (0.74 to 1.26)0.81
 ACR 2: discoid rash0.77 (0.56 to 1.07)0.12
 ACR 3: photosensitivity0.93 (0.70 to 1.22)0.59
 ACR 4: oral ulcer0.94 (0.71 to 1.26)0.68
 ACR 5: arthritis0.99 (0.73 to 1.34)0.95
 ACR 6: serositis1.19 (0.91 to 1.56)0.21
 ACR 7: renal disorder1.20 (0.91 to 1.59)0.20
 ACR 8: neurological disorder1.16 (0.75 to 1.80)0.50
 ACR 9: haematological disorder1.05 (0.80 to 1.37)0.74
 ACR 10: immunological disorder1.44 (1.08 to 1.93)0.014
 ACR 11: ANA1.04 (0.38 to 2.87)0.94
Antibodies
 dsDNA1.47 (1.07 to 2.01)0.018
 Sm0.91 (0.57 to 1.46)0.71
 Cardiolipin*†1.01 (0.76 to 1.35)0.93
 Lupus anticoagulant1.08 (0.76 to 1.53)0.68
 β2-glycoprotein†1.20 (0.84 to 1.72)0.33
 SSA1.17 (0.89 to 1.53)0.26
 SSB1.09 (0.80 to 1.50)0.58
Complement
 Low C3/C4/CH50‡1.21 (0.90 to 1.64)0.21
  • Values in bold indicate p<0.05.

  • *ORs for PRSs in the highest quartile compared with quartiles 1–3.

  • †IgM or IgG.

  • ‡Low complement levels defined according to the SLICC-12 criteria.24

  • ACR, American College of Rheumatology; dsDNA, double-stranded DNA; PRS, polygenic risk score; SLICC, Systemic Lupus International Collaborating Clinics; SSA, Sjögren’s syndrome-related antigen A; SSB, Sjögren’s syndrome-related antigen B.