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

Table 2B.

The association of key clinical outcome measures with autoantibody subgroups.

Lowest ever CMASa median (IQR) Highest ever PGAb median (IQR) Ever received biologic drug (%) Ever received IV cyclophosphamide (%)
Total cohort (n = 379)c 40 (24.5–47.5) 4 (2.2–7.0) 77 (20) 89 (23)
Anti-TIF1γ
(n = 68)
40 (25–47)** 5.2 (2.6–7.6) 23 (34)** 25 (37)*
Anti-NXP2
(n = 59)
29.5 (16–43)*** 4.6 (2.7–6.9) 11 (19) 10 (17)
Anti-MDA5
(n = 23)
45 (38–52)*** 4.1 (3.1–6.7) 1 (4) 6 (26)
Anti-PmScl
(n = 20)
45.5 (22–49) 3 (1.5–6.9) 3 (15) 5 (25)
Anti- Mi2
(n = 15)
29 (15–38)*** 4.8 (2.45–7) 1 (7) 3 (20)
Anti-U1RNP
(n = 14)
46.5 (42–49)*** 3.4 (1–5.2) 2 (14) 1 (7)
Anti-SRP
(n = 7)
26 (9.842)*** 6.6 (3.5–6.9) 2 (29) 2 (29)
Anti-synthetased
(n = 6)
44.5 (41–48) 3.3 (2.4–5.5) 1 (17) 2 (33)
Anti-HMGCR
(n = 4)
15 (1–30)*** 6.6 (4.4–8.6) 4 (100) 2 (50)
Anti-SAE
(n = 3)
39 (23–47) 3.5 (2–7) 0 0
Othere
(n = 5)
40 (25–47)** 4.1 (2.3–7) 2 (40) 1 (20)
Nil identifiedf
(n = 155)
43 (27–48) 3.2 (2.0–6.0) 28 (18) 32 (21)

Statistically significant associations are highlighted in bold.

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

CMAS; Childhood Myositis Assessment Score, PGA; Physician Global Assessment of disease activity.

a

Data available for 355 patients.

b

Data available for 370 patients.

c

Including 8 patients with other idiopathic inflammatory myopathy.

d

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

e

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

f

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