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Table 2 Clinical features of SSc patientsa

From: Altered monocyte and fibrocyte phenotype and function in scleroderma interstitial lung disease: reversal by caveolin-1 scaffolding domain peptide

Patient characteristics

Patients

Controls

Caucasian males, n

3

9

Caucasian females, n

4

12

African-American males, n

1

2

African-American females, n

4

2

Asian females, n

1

1

Smokers, n

1

0

Former smokers, n

3

0

Mean age ± SD, years (range)

54.6 ± 9.8 (39 to 75)

43.7 ± 9.4 (22 to 57)

Disease: limited cutaneous, n

0

Not applicable

   Diffuse cutaneous

9

Not applicable

   Overlap

4

Not applicable

Disease duration, years: mean ± SD (range)

9.4 ± 6.6 (1 to 22)

Not applicable

Pulmonary involvement (ILD)

13 of 13 (100%)

Not applicable

Pulmonary Hypertension

5 of 13 (38.5%)

Not applicable

GI involvement

12 of 13 (92.3%)

Not applicable

Cardiac involvement

7 of 13 (53.8%)

Not applicable

Renal involvement

0 of 13 (0%)

Not applicable

Autoantibodies: ANA+

11 of 11 (100%)

Not applicable

   Scl-70+

4 of 11 (36%)

Not applicable

   Anticentromere

0 of 10 (0%)

Not applicable

  1. aSSc, systemic sclerosis; SD, standard deviation; ILD, interstitial lung disease; GI, gastrointestinal; ANA, antinuclear antibody.