Table 1

Clinical characteristics of the patients in the IIM subgroups and the non-IIM group

DM
(n=36)
ADM
(n=17)
PM
(n=19)
Non-IIM*
(n=16)
p<0.05
Age (years), mean (SD)53.5 (14.3)50.5 (11.7)64.1 (11.4)54.6 (15.8)DM versus PM
ADM versus PM
Female, n (%)24 (66.7)8 (47.1)12 (63.2)11 (68.8)NSD
Muscle weakness, n (%)34 (94.4)2 (11.8)15 (79.0)10 (62.5)DM versus ADM
DM versus non-IIM
ADM versus PM
ADM versus non-IIM
Myalgia, n (%)24 (66.7)11 (64.7)8 (42.1)8 (50.0)NSD
CK level (IU/litre), mean (SD)1771.9 (2557.8)394.6 (586.9)1840.1 (1651.4)1423.1 (1456.7)DM versus ADM
ADM versus PM
ADM versus non-IIM
Time from onset of symptoms to first MRI (days), mean (SD)157.9 (243.6)205.4 (394.6)495.6 (622.0)454.4 (711.5)DM versus PM
Muscle biopsy performed, n (%)29 (80.6)10 (58.8)15 (78.9)9 (86.7)†NSD
Inflammatory cell infiltration in muscle, n (%)25 (86.2)7 (70.0)15 (100.0)9 (100.0)NSD
  • *Non-IIM included anti-ARS antibody-positive myositis (n=4), definite or probable PM by the Bohan and Peter criteria (n=4), anti-mitochondrial antibody-positive myositis (n=3), SLE (n=2), SSc (n=2) and MCTD (n=1).

  • †Muscle biopsy was performed in nine patients with non-IIM: anti-ARS antibody-positive myositis (n=2), definite or probable PM by the Bohan and Peter criteria (n=3), anti-mitochondrial antibody-positive myositis (n=2), SLE (n=1), SSc (n=1).

  • ADM, amyopathic dermatomyositis;ARS, aminoacyl-tRNA synthetases;CK, creatine kinase;DM, dermatomyositis;IIM, idiopathic inflammatory myopathy;MCTD, mixed connective tissue disease; NSD, no significant differences among the subgroups;PM, polymyositis;SLE, systemic lupus erythematosus;SSc, systemic sclerosis.