Table 1

Patient details and antibody frequencies


n (%)


Polymyositis
Dermatomyositis


(n = 117)
(n = 108)

Females
81 (69.2)
75 (69.4)
Average age of onseta
50.4 ± 14.5
49.0 ± 14.1
Interstitial lung disease
18 (15.4)
19 (17.6)
Malignancyb
2 (1.7)
14 (13.0)
Antibody status
(n = 105)
(n = 101)
Myositis-specific antibodies


     Jo-1
24 (22.9)
22 (21.8)
     PL-7
1 (1.0)
0
     PL-12
0
1 (1.0)
     EJ
0
1 (1.0)
     OJ
1 (1.0)
1 (1.0)
     KS
1 (1.0)
1 (1.0)
     Any of the abovec
27 (25.7)
25 (24.7)
     Mi-2d
1 (1.0)
17 (16.8)
     SRP
5 (4.8)
2 (2.0)
Myositis-associated antibodies


     U1-RNP
5 (4.8)
8 (7.9)
     U3-RNP
0
2 (2.0)
     Ku
0
2 (2.0)
     PM-Scl
5 (4.8)
6 (5.9)
None of the above autoantibodies
62 (59.1)
45 (44.5)

aResults expressed as mean ± standard deviation. bDermatomyositis (DM) versus polymyositis (PM), p = 0.001; odds ratio (OR) 8.6, (95% confidence interval (CI) 1.9–78.9). cThe total for DM is 25 despite the presence of 26 anti-tRNA synthetases, due to one patient possessing both anti-Jo-1 and anti-PL-12. dDM versus PM, p = 2.9 × 10-5; OR 21.0 (95% CI 3.1–887.7).

Chinoy et al. Arthritis Research & Therapy 2006 8:R13   doi:10.1186/ar1862

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