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. 2018 Jan 15;33(3):322–327. doi: 10.5606/ArchRheumatol.2018.6630

Table 2. Comparison of systemic sclerosis patients with interstitial lung disease and those not.

Clinical features SSc with ILD (n=43) SSc without ILD (n=65)  
  n % Mean±SD n % Mean±SD p
Age (year)     51.34±14.55     49.23±13.51 0,49
Gender             0,92
Female 38     57      
Male 5     8      
Duration (year)     6.72±5.02     4.28±3.50 0.012*
Subtype             0,33
Diffuse 22     27      
Limited 21     38      
Antinuclear antibody (+) 42 97,7   62 95,4   0,54
Anti-scleroderma 70 (+) 27 62,8   10 15,4   <0.001
Anti-centromere (+) 4 9,3   33 50,8   <0.001
White blood cells (µL)     7650.9±2656.2     6469.0±1858.1 0.022*
Platelet (¥103/µL)     282.1±81.7     241.3±66.5 0.007*
Erythrocyte sedimentation rate (mm/h)     39.4±27.3     26.5±22.0 0.008*
C-reactive protein (mg/dL)     1.2±3.1     0.3±1.4 0,1
Raynaud’s phenomenon 42 97,7   64 98,5   0,77
Sclerodactyly 38 88,4   59 90,8   0,69
Skin rash 11 25,6   17 26,2   0,95
Digital ulcer 15 34,9   12 17,9   0,06
Arthritis 23 53,5   34 52,3   0,91
Gastrointestinal involvement 21 48,8   23 35,4   0,17
Pulmonary hypertension 11 25,6   2 3,1   <0.001*
SSc: Systemic sclerosis; ILD: Interstitial lung disease; SD: Standard deviation; * p-value <0.05.