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Table 3 Comparison of variables between patients who were newly classified as systemic sclerosis according to the 2013 ACR/EULAR classification criteria for systemic sclerosis and those who had been previously classified

From: Application of the 2013 ACR/EULAR classification criteria for systemic sclerosis to patients with Raynaud’s phenomenon

Variables

Patients newly classified as systemic sclerosis (N = 17)

Patients previously classified as systemic sclerosis (N = 60)

P value

P value *

Characteristics

    

  Age (years old)

48.9 ± 12.4

51.1 ± 13.1

NS

 

  Sex, female (N (%))

17 (100)

52 (86.7)

NS

 

The 2013 ACR/EULAR classification criteria score

10.5 ± 1.8

19.1 ± 5.1

<0.001

<0.001

Clinical manifestations (N (%))

    

  Scleroderma (proximal)

0 (0)

40 (66.7)

<0.001

<0.001

  Puffy finger

12 (70.6)

27 (45.0)

NS

 

  Sclerodactyly

6 (35.2)

55 (91.7)

<0.001

<0.001

  Digital tip ulcer

2 (11.8)

20 (33.3)

NS

 

  Fingertip pitting scar

0 (0)

19 (31.7)

0.008

0.016

  Telangiectasia

5 (29.4)

5 (8.3)

0.022

0.044

  Abnormal nailfold capillaries

17 (100)

56 (93.3)

NS

 

  Pulmonary arterial hypertension

0 (0)

3 (5.0)

NS

 

  Interstitial lung disease*

2 (11.8)

29 (48.3)

0.007

0.014

Autoantibodies (N (%))

    

  Antinuclear antibody (centromere)

9 (52.9)

12 (20.0)

0.007

0.014

  Anti-centromere antibody

11 (64.7)

13 (21.6)

0.001

0.002

  Anti-Scl-70 antibody

0 (0)

29 (48.3)

<0.001

<0.001

  1. Values are expressed as N (%) or mean ± standard deviation. P value* = Bonferroni-adjusted P value among variables with statistical significance. ACR, American College of Rheumatology; EULAR, The European League Against Rheumatism; NS, not significant.