Table 5.

Variables from time of diagnosis in 49 juvenile MCTD patients according to left ventricular function at examination after a median 14.9 years of disease duration.

Variables Assessed at DiagnosisNormal LV Function, n = 41LV Dysfunction, n = 8p
Age, yrs14.7 (4.6)12.3 (2.8)0.106
Puffy hands17 (42)4 (50)0.710
RP40 (98)8 (100)1.000
SLE-like disease39 (95)8 (100)1.000
  Arthritis36 (88)7 (88)0.981
  Lymphadenopathy5 (12)2 (25)0.344
  Facial erythema10 (24)3 (38)0.422
  Cytopenia5 (12)3 (38)0.110
  Pericarditis/pleuritis2 (5)01.000
SSc-like disease11 (27)2 (25)0.944
  Sclerodactyly4 (10)01.000
  Pulmonary fibrosis5 (12)2 (25)0.320
  Esophagus dysmotility1 (2)1 (13)0.303
PM-like disease10 (24)5 (63)0.047
  High CK7 (17)4 (50)0.063
  Muscle weakness9 (22)5 (63)0.033
No. active joints4.0 (2.0–10.0)11.5 (4.0–22.3)0.099
ESR, mm/h20.0 (12.0–30.5)23.5 (16.0–48.3)0.417
CRP, mg/l, n = 414.0 (1.9–7.4)7.0 (4.3–21.8)0.081
CRP at diagnosis or during 1st yr4.0 (2.0–7.4)7.0 (4.3–21.8)0.049
Prednisolone dose, mg0 (0–13.8)20.0 (0–45.0)0.057
RF-positive, n = 4221 (62)5 (63)1.000
RF-positive during 1st yr23 (56)5 (63)1.000
Medications after 1st yr
  Prednisolone13 (32)5 (63)0.230
  Antimalarials20 (49)4 (50)1.000
  MTX16 (39)5 (63)0.437
  NSAID12 (29)5 (63)0.089
  Calcium antagonist5 (12)2 (25)0.378
  • Values are in n (%) or median (IQR). Values in bold face are statistically significant. MCTD: mixed connective tissue disease; LV: left ventricular; SLE: systemic lupus erythematosus; SSc: systemic sclerosis; PM: polymyositis; CK: creatine kinase; ESR: erythrocyte sedimentation rate; CRP: C-reactive protein; RF: rheumatoid factor; NSAID: nonsteroidal antiinflammatory drugs; IQR: interquartile range; RP: Raynaud phenomenon; MTX: methotrexate.