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Table 1 Patient characteristics (n = 1140)

From: The association of low complement with disease activity in systemic sclerosis: a prospective cohort study

Characteristic

n (%) or mean ± SD

Age at diagnosis, years

46.0 ± 14.1

Age at recruitment, years

57.4 ± 12.3

Follow-up duration, years

3.4 ± 1.7

Sex

 Male

148 (13.0 %)

 Female

992 (87.2 %)

Race

 White

1012 (93.3 %)

 Asian

50 (4.7 %)

 Australian Aboriginal or Torres Strait Islander

14 (1.3 %)

 Other

9 (0.9 %)

Disease duration at recruitmenta

11.3 ± 9.9

  ≤ 2 years

163 (14.3 %)

  ≤ 5 years

356 (31.2 %)

Disease subtypeb

 Diffuse

310 (27.2 %)

 Limited

830 (72.8 %)

Overlap disease features present everc

267 (23.4 %)

 Rheumatoid arthritis

22 (1.9 %)

 Polymyositis

6 (0.5 %)

 Dermatomyositis

1 (0.01 %)

 Sjögren’s syndrome

21 (1.8 %)

 SLE

9 (0.8 %)

Serological profile at recruitment

 Anti-centromere ANA

517 (46.2 %)

 Anti-Scl-70 antibodies

167 (15.2 %)

 Anti-RNAP antibodies

84 (13.3 %)

 Anti-U1 RNP antibodies

22 (2.0 %)

 Anti-Ro antibodies

72 (6.6 %)

 Anti-La antibodies

18 (1.6 %)

 Anti-Sm antibodies

6 (0.6 %)

 Anti-PM-Scl antibodies

15 (1.4 %)

 Anti-dsDNA antibodies

26 (3.1 %)

 Anti-Jo-1 antibodies

5 (0.5 %)

 ANCA

134 (12.9 %)

  MPO specificity

17 (1.6 %)

  PR-3 specificity

22 (2.1 %)

 Rheumatoid factor

288 (27.2 %)

 Anti-phospholipid antibodies

272 (25.7 %)

  Cardiolipin IgM

165 (65.0 %)

  Cardiolipin IgG

105 (39.3 %)

 Anti-β2-glycoprotein antibody

84 (33.0 %)

 Lupus anticoagulant

26 (3.1 %)

  1. Abbreviations: ANA Anti-nuclear antibody, Anti-Scl-70 Anti-scleroderma-70 antibodies, Anti-U1 RNP Anti-ribonucleoprotein antibodies, Anti-Sm Anti-Smith antibodies, Anti-PM-Scl Anti-polymyositis scleroderma antibodies, Anti-dsDNA Anti-double-stranded DNA antibodies, Anti-RNAP Anti-RNA polymerase antibodies, ANCA Anti-neutrophil cytoplasmic antibodies, MPO Myeloperoxidase, PR-3 Proteinase-3
  2. aSince onset of first non-Raynaud’s phenomenon disease manifestation
  3. bDisease subtype based on extent of skin involvement, with limited disease being confined to the extremities distal to elbows and knees, as well as the face
  4. cActual overlap disease features specified for only a proportion of patients classified by the treating physician as having ‘SSc overlap syndrome’