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. 2017 Nov;84:55–64. doi: 10.1016/j.jaut.2017.06.007

Table 2A.

The association of key clinical disease features with autoantibody subgroups.

Classified as PM (%) Dysphagiaa (%) Calcinosisa (%) Ulcerationa (%) Oedemaa (%) Lipoatrophya (%) Arthritisa (%)
Total cohort (n = 379)b 10 (2.6) 96 (26) 120 (32) 76 (20) 155 (41) 57 (15) 148 (40)
Anti-TIF1γ
(n = 68)
0 18 (26) 25 (37) 23 (34)*** 32 (47) 13 (19) 26 (38)
Anti-NXP2
(n = 59)
0 17 (29) 25 (43) 8 (14) 26 (44) 9 (16) 20 (34)
Anti-MDA5
(n = 23)
0 7 (30) 7 (27) 11 (50)*** 10 (43) 3 (13) 15 (65)*
Anti-PmScl
(n = 20)
0 5 (25) 11 (55)* 4 (20) 5 (25) 6 (30)* 11 (44)
Anti- Mi2
(n = 15)
0 7 (47)* 4 (27) 0 11 (73)* 2 (13) 6 (40)
Anti-U1RNP
(n = 14)
3 (21)*** 6 (43) 1 (8) 2 (14) 2 (14) 2 (14) 7 (50)
Anti-SRP
(n = 7)
2 (29)*** 3 (43) 1 (14) 4 (50)** 5 (71) 1 (13) 2 (29)
Anti-synthetasec
(n = 6)
0 0 1 (17) 2 (33) 3 (50) 2 (33)* 2 (33)
Anti-HMGCR
(n = 4)
2 (50)*** 3 (75)* 0 0 0 0 0
Anti-SAE
(n = 3)
0 0 1 (33) 1 (33) 1 (33) 1 (33) 2 (66)
Otherd
(n = 5)
1 (20)** 3 (60) 1 (20) 2 (50) 1 (20) 2 (50) 3 (60)
Nil identifiede
(n = 155)
2 (1) 27 (17) 44 (28) 19 (12) 59 (38) 16 (10) 54 (35)

Statistically significant associations are highlighted in bold.

*P < 0.05, **P < 0.01, ***P < 0.001, PM; polymyositis.

a

Data available for 374 patients.

b

Including 8 patients with other idiopathic inflammatory myopathy.

c

3 patients anti-Jo-1, 2 patients anti-PL12 and 1 patient anti-PL7.

d

1 anti-Ku, 1 anti-Scl70, 1 anti-Ro60, 1 anti-U3RNP, 1 anti-mitochondrial antibody.

e

No known autoantibody identified using the techniques described (42% of this group have unidentified bands visible on immunoprecipitation).