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. Author manuscript; available in PMC: 2011 Jan 1.
Published in final edited form as: Ann Neurol. 2010 Jan;67(1):53–63. doi: 10.1002/ana.21805

Table 1.

Fold-ratio compared to normal for microarray measured ISG15 pathway transcripts in dermatomyositis muscle with and without PFA (DM-PFA N=7 and DM-NO-PFA N=7) compared to other inflammatory myopathies (OtherIM; N=62), both compared to normal muscle (N=12). ISG15 pathway transcript elevation for ISG15, HERC5, and USP18 are relatively specific to DM and highly specific to patients with DM and the presence of perifascicular atrophy (PFA) present on H&E stained muscle sections.

Transcript Ubiquitin-like
(Ubl) role
DM-PFA
Fold
DM-NO-
PFA
OtherIM-
Fold
p-value
All DM vs
Other IM
p-value
DM-PFA vs
DM-NO-PFA
ISG15 Ub-like modifier 339 49/13* 8 0.001 0.0001
Ube1L E1 enzyme 9 2/2* 3 0.160 0.0317
Ube2L6 E2 enzyme 21 6/6* 6 0.018 0.0007
HERC5 E3 enzyme 62 6/1.7* 1.2 0.010 0.0093
USP18 De-Ubl enzyme 68 6/1.7* 1.3 0.005 0.0013

1 of 7 DM-NO-PFA samples had very high ISG15, HERC5, and USP18 transcript levels as shown in Figure 1D; the mean fold-ratios for the remaining 6 DM-NO-PFA samples is indicated by *.