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. 2018 Jan 21;24(3):387–396. doi: 10.3748/wjg.v24.i3.387

Table 4.

Prevalence of anti-neutrophil cytoplasmic antibodies in biliary atresia patients and non-biliary atresia controls n (%)

Variable BA, n = 124 Other liver diseases1, n = 92 Healthy, n = 48
ANCA, by IIF 36 (29.0)a 23 (25.0) 2 (4.2)
c-ANCA 10 (8.1) 1 (1.1) 0 (0)
p-ANCA 25 (20.2) 21 (22.8) 2 (4.2)
a-ANCA 1 (0.8) 1 (1.1) 0 (0)
Specific ANCA, by ELISA
Anti-MPO 11 (8.9) 6 (6.5) 2 (4.2)
Anti-PR3 19 (15.3) 13 (14.2) 0 (0)
Anti-MPO and/or anti-PR3 23 (18.0)a 13 (14.2) 2 (4.2)
ANCAs 47 (37.9)a 31 (33.7) 3 (6.3)
1

Choledochal cysts, transient cholestasis of unknown origin, and neonatal intrahepatic cholestasis caused by citrin deficiency were included as disease controls.

a

P < 0.05 vs healthy controls. Anti-MPO and/or anti-PR3: Any positivity of specific ANCAs; ANCAs: Any positivity of ANCAs by IIF or specific ANCA by ELISA. ANCA: Anti-neutrophil cytoplasmic antibody; BA: Biliary atresia; ELISA: Enzyme linked immunosorbent assay; IIF: Indirect immunofluorescence.