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Table 1 Characteristics of SSc patients and patients with VEDOSS

From: Role of lectin pathway complement proteins and genetic variants in organ damage and disease severity of systemic sclerosis: a cross-sectional study

Characteristics

SSc patients

(n = 211)

UCTD

(n = 29)

All patients (n = 240)

Female, %

79

93

80

Age (years), mean (SD)

60 (13)

51 (14)

59 (14)

Caucasian race, %

97

100

97

Duration since RP onset (years), mean (SD)

14 (12)

8 (10)

13 (12)

Duration since first non-RP (years), mean (SD)

13 (11)

na

na

Diffuse disease, %

18

na

na

Autoantibodies, %

 Anti-topoisomerase I (Scl-70)

29

7

 

 Anti-centromere

45

34

 

 Anti-RNA polymerase III

8

3

 

Organ involvement,%

 Esophageal symptoms

48

31

45

 Pulmonary hypertension

15

0

13

 Interstitial lung disease

49

0

42

 Renal crisis

2

0

2

Disease activity/severity

 Digital ulcers, %

12

0

10

 mRSS, median (IQR)

4 (2–9)

0 (0–0)

3 (0–9)

 EUSTAR SSc activity score, median (IQR)

1 (0.5–2.0)

na

na

 FVC (% predicted), mean (SD)

98 (21)

99 (15)

98 (20)

 DLCO/va (% of predicted), mean (SD)

79 (16)

94 (17)

82 (17)

 DLCO/sb (% of predicted), mean (SD)

71 (19)

96 (13)

74 (20)

  1. Abbreviations: DLCO diffusing capacity of the lung for carbon monoxide, EUSTAR European Scleroderma Trials and Research Group, FVC forced vital capacity, mRSS modified Rodnan skin score, RP Raynaud’s phenomenon, SD standard deviation, SSc systemic sclerosis, na not applicable