Table 1.

Characteristics of the study population.

ControlsPsAP
No. patients24,1804836-
SLE cases36 (0.15)18 (0.37)0.001
Age, yrs, mean ± SD56.25 ± 15.2656.31 ± 15.24NS
Sex, female13,015 (53.8)2603 (53.8)NS
SES
      19082 (40.6)1552 (32.2)< 0.0001
      28336 (37.3)1958 (40.7)< 0.0001
      34956 (22.2)1306 (27.1)< 0.0001
Smokers9220 (38.3)2051 (42.5)< 0.0001
Ethnicity
      Arab4369 (18.5)612 (12.7)< 0.0001
      Jewish19,296 (81.5)4224 (87.3)
BMI, mean ± SD27.47 ± 5.4428.65 ± 5.80< 0.0001
Comorbidity
      Hyperlipidemia13,541 (56)3125 (64.6)< 0.0001
      Hypertension8383 (34.7)2035 (42.1)< 0.0001
      DM5339 (22.1)1353 (28)< 0.0001
      Malignancy2709 (11.2)980 (20.3)< 0.0001
      Osteoporosis2376 (9.8)623 (12.9)< 0.0001
      Obesity6790 (28.1)1851 (38.3)< 0.0001
      CHF758 (3.2)218 (4.5)< 0.0001
      IHD3000 (12.4)766 (15.8)< 0.0001
      CVA1312 (5.4)304 (6.3)0.017
cDMARD578 (2.4)4090 (84.6)< 0.0001
bDMARD
      Anti-TNF-α97 (0.4)1779 (36.8)< 0.0001
Possible SLE-inducing medication used prior to SLE diagnosis
      Statins5 (0.02)7 (0.15)0.001
      PPI12 (0.05)5 (0.1)NS
      Beta blockers1 (0.004)2 (0.04)0.07
      ACEi7 (0.03)1 (0.02)NS
      Thiazides7 (0.03)1 (0.02)NS
      Anti-TNF-α0 (0.0)2 (0.04)0.028
  • Values are n (%) unless otherwise specified. The percentages reported were calculated from the actual number, not including missing data. ACEi: angiotensin-converting enzyme inhibitor; anti-TNF-α: anti–tumor necrosis factor-α; bDMARD: biological disease-modifying antirheumatic drug; cDMARD: conventional disease-modifying antirheumatic drug; CHF: congestive heart failure; CVA: cerebrovascular accident; DM: diabetes mellitus; IHD: ischemic heart disease; NS: not significant; PPI: proton pump inhibitor; PsA: psoriatic arthritis; SES: socioeconomic status; SLE: systemic lupus erythematosus.