Table 2

Association of myositis-specific antibodies with clinical phenotype in patients with IIM

PhenotypeMarkerAlphadiaEuroimmunTrinity
PosPosNegNegP valuePosPosNegNegP valuePosPosNegNegP value
PosNegPosNegPosNegPosNegPosNegPosNeg
MalignancyTif1-γ12101310.213531481190.124041271210.0212
NXP-2 (MORC3)2691270.115514101290.331816101270.4337
DM skin lesionsMi-26253830.06386553800.35825454810.4873
TIF-γ3056850.06671614384<0.00011424583<0.0001
NXP-2 (MORC3)4455810.71663256830.40034355820.4449
MDA-55254830.12288251830.01596453810.3176
SAE4155840.15904055850.02654255830.2273
Amyopathic DMMDA-52551320.03802851290.07582851290.0758
CalcinosisNXP-2 (MORC3)2671290.08012371320.0316752130<0.0001
Inclusion body myositisCN-1A11851200.5791
ArthritisJo-1141710103<0.0001131611104<0.00011014141060.0003
Jo-1, PL7, PL12 or EJ1621899<0.000116218990.00011218121020.0004
ILDJo-119121398<0.0001191013100<0.000115917101<0.0001
Jo-1, PL7, PL12 or EJ22151095<0.00012317993<0.000117131597 97<0.0001
RaynaudJo-1121813990.0003131512102<0.0001914161030.0063
Jo-1, PL7, PL12 or EJ1620997<0.00011722895<0.0001111814990.0013
  • The association was evaluated by χ2 testing or Fisher’s exact test (if cell size was <10) using Analyse-it for Excel.

  • IIM, inflammatory myopathy.