Table 1.

Demographic and clinical characteristics of the 120 patients with SSc. Arterial hypertension: blood pressure above 140/90 mmHg at study inclusion.

CharacteristicsAlllcSScdcSSc
Patients
  Sex, n, males/females19/1013/7616/25
  Age, yrs, mean ± SD (range)57 ± 12 (22–79)59 ± 1155 ± 12
  Disease duration, yrs, mean ± SD (range)12 ± 9 (0–53)12 ± 911 ± 9
Cutaneous involvement
  mRSS, mean ± SD11 ± 97 ± 320 ± 9
  Cutaneous ulcers, n221012
  Calcinosis, n (N)*43 (107)3013
Pulmonary and cardiac involvement
  DLCO, mean ± SD % predicted (N)*65.1 ± 19.2 (118)64.2 ± 18.5 (77)66.2 ± 20.5 (41)
  FVC, mean ± SD % predicted (N)*95.6 ± 21.2 (118)99.3 ± 20.1 (77)88.8 ± 21.8 (41)
  Radiographic confirmed lung fibrosis, n21147
  Elevated SPAP by echocardiography, n (N)*10 (115)64
Serology, n
  Antinuclear antibodies1157441
  Anti-Scl-70 antibodies15312
  Anticentromere antibodies48417
  DMARD743
  Current or previous smokers825725
  Arterial hypertension301812
Blood samples
  Leukocytes, × 109/l, mean ± SD7.2 ± 2.37.4 ± 2.57.7 ± 2.4
  Neutrophils, × 109/l, mean ± SD4.6 ± 1.94.7 ± 2.04.9 ± 2.2
  Platelets, × 109/l, mean ± SD272 ± 85265 ± 86269 ± 61
  Lactate dehydrogenase, U/l, mean ± SD186 ± 37191 ± 40185 ± 37
  • * Reduced number of patients because of lack of information. N: total number of subjects in the group; SSc: systemic sclerosis; lcSSc: limited cutaneous SSc; dcSSc: diffuse cutaneous SSc; mRSS: modified Rodnan Skin score; FVC: forced vital capacity; SPAP: systolic pulmonary artery pressure; DMARD: disease-modifying antirheumatic drug.