Table 4.

Assessment of risk factors for SLE development in the PsA group.

PsA Patients With SLE, n = 18PsA Patients Without SLE, n = 131Univariable ModelaMultivariate Model IbMultivariate Model IIc
ORCI 95%PORCI 95%PORCI 95%P
Age at PsA diagnosis, yrs, mean ± SD47.12 ± 18.2338.9 ± 15.361.251.09–1.420.0011.251.06–1.480.008
PsA duration, yrs, mean ± SD2.39 ± 5.336.49 ± 7.700.860.73–1.010.060.820.69–.980.03
Anti–TNF-α2 (11.1)16 (12.2)1.220.23–6.530.820.860.1–7.290.890.950.1–8.150.96
Statins7 (38.9)24 (18.3)6.811.55–29.840.0112.491.73–90.290.019.861.09–89.260.042
PPI5 (27.8)56 (42.7)0.660.20–2.230.51.170.28–4.950.831.50.30–6.700.60
Beta blockers2 (11.1)8 (6.1)2.420.45–13.090.34.170.53–32.990.184.760.57–39.550.150
ACEi28 (21.4)1 (5.6)0.240.03–2.030.190.040.001–1.620.090.340.01–2.030.10
Thiazides12 (9.2)1 (5.6)0.787.750.8321.250.37–1215.030.1429.600.45–1972.721.11
  • Values are n (%) unless otherwise specified.

  • a Logistic regression was performed separately for each item.

  • b Multivariate Model I includes PsA duration.

  • cMultivariate Model II includes age at PsA diagnosis. ACEi: angiotensin-converting enzyme inhibitor; anti-TNF-α: anti–tumor necrosis factor-α; PPI: proton pump inhibitor; PsA: psoriatic arthritis; SLE: systemic lupus erythematosus.