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Table 1 Demographic and clinical features of patients with systemic sclerosis and controls

From: Microparticles: potential new contributors to the pathogenesis of systemic sclerosis?

Variable

Scleroderma patients

(n = 70)

Healthy controls

(n = 35)

p

Female/male

63 (90)/7 (10)

31 (88.5)/4 (11.4)

0.680

Age, in years

48.9 ± 13.4

47.6 ± 14.0

0.630

Limited SSc/diffuse SSc

44 (62.9)/26 (37.1)

Disease duration, in years

6.4 ± 4.0

Modified Rodnan skin score

6.5 ± 9.6

Digital ulcers ever

39 (55.7)

Forced vital capacity, in % predict

80.9 ± 17.4 (n = 63)

Forced vital capacity ≤ 80%

33 (52.3) (n = 63)

Interstitial lung disease

38 (54.3)

Pulmonary arterial hypertension

4 (5.7)

Esophageal dyskinesia

42 (60)

Cardiac involvement

8 (11.4)

Scleroderma renal crisis

3 (4.3)

Autoantibodies

   

 Anticentromere

13 (18.6)

 Anti-topoisomerase I

13 (18.6)

Comorbidity

37 (52.9)

Nailfold capillaroscopy SD pattern

(n = 61)

  

 Early

8 (11.4)

 Active

25 (35.7)

 Late

28 (40)

  

Nailfold capillaroscopy parameters

(n = 61)

  

 Mean capillaries loops/mm

7.2 ± 2.0

 Mean enlarged capillaries

2.1 ± 1.5

 Mean microhemorrhages

1.5 ± 2.2

 Mean giant capillaries

0.2 ± 0.4

 Mean avascular score

1.0 ± 0.9

 Avascular score > 1.5

19 (31.1)

Calcium channel blockers use

49 (70)

Phosphodiesterase-5 inhibitors use

9 (12.9)

Statins use

8 (11.4)

Use of immunosuppressants

   

 Any

39 (55.7)

 Glucocorticoids

8 (11.4)

 Mean prednisone dosage, in mg/day

0.8 ± 2.5

 Cyclophosphamide

3 (4.3)

 Mycophenolate

15 (21.4)

 Azathioprine

3 (4.3)

 Rituximab

1 (1.4)

 Methotrexate

12 (17.1)

 Leflunomide

4 (5.7)

 
  1. Data are expressed as mean ± standard deviation or n (%)
  2. SD, scleroderma; SSc, systemic sclerosis