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Table 1 Characteristics of cases and controls

From: Potential role of the lectin pathway of complement in the pathogenesis and disease manifestations of systemic sclerosis: a case-control and cohort study

Characteristics

Cases

Controls

(n = 90)

(n = 90)

Female, n (%)

78 (87)

78 (87)

Age (years), mean (SD)

60 (15)

59 (16)

Race, n (%)

  

  Caucasian

76 (84)

 

  Asian

9 (10)

 

  Other

5 (6)

 

Duration of disease (years), mean (SD)

14.3 (10.3)

 

SSc subtype, n (%)

  

  Diffuse disease

23 (26)

 

  Limited disease

62 (69)

 

  Sine

1 (1)

 

  Mixed connective tissue disease

4 (4)

 

Autoantibodies, n (%)

  

  Anti-topoisomerase I (Scl-70)

17 (19)

 

  Anti-centromere

38 (42)

 

  Anti-RNA polymerase III

8 (9)

 

Organ involvement, n (%)

  

  Bowel dysmotility

9 (10)

 

  Pulmonary arterial hypertension

8 (9)

 

  Interstitial lung disease

41 (46)

 

  Renal crisis

4 (4)

 

  Gastroesophageal reflux disease

83 (92)

 

Disease activity/severity

  

  Active digital ulcers, n (%)

13 (14)

 

  mRSS, mean (SD)

8.9 (7.3)

 

  SSc HAQ, mean (SD)

20.5 (13.4)

 

  EUSTAR SSc activity score, mean (SD)

2.2 (1.7)

 

  Immunosuppressive agents, n (%)

28 (31)

 

  Past treatment with iloprost, n (%)

17 (19)

 

  FVC (% predicted), mean (SD)

91.5 (22.5)

 

  DLCO (% predicted), mean (SD)

58.5 (18.8)

 

  6MWD (meter), mean (SD) meters

471.7 (126.1)

 
  1. 6MWD, six-minute walk distance; DLCO, diffusing capacity of the lung for carbon monoxide; EUSTAR, EULAR Scleroderma Trials and Research Group; FVC, forced vital capacity; mRSS, modified Rodnan skin score; SD, standard deviation; SSc, systemic sclerosis; SSc HAQ, Scleroderma Health Assessment Questionnaire.