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. 2021 Jul 12;33(5):521–529. doi: 10.1097/MOP.0000000000001045

Table 4.

Aetiology table and accompanying diagnostic work-up for children with IBD and nonacute abnormal liver blood tests

Causes Diagnostic tests
Immune-related liver disease
 Autoimmune hepatitis (AIH) Auto-antibodies (antimitochondrial, antismooth muscle, antinuclear and antiliver-kidney-microsome)
Immunoglobulin G
Liver histology (interface hepatitis)
 Primary sclerosing cholangitis (PSC) MR cholangiopancreatography
 Autoimmune sclerosing cholangitis (ASC) Auto-antibodies (antimitochondrial, antismooth muscle, antinuclear and antiliver-kidney-microsome)
Immunoglobulin G
MR cholangiopancreatography
Liver histology (interface hepatitis and bile duct involvement)
Viral hepatitis
Hepatitis A (IgM)
Hepatitis B (HBsAg, anti-HBc IgM, anti-HBs)
Hepatitis C (Anti-HCV, HCV RNA)
Hepatitis E (IgM, HEV RNA
Cytomegalovirus (IgM, CMV-DNA)
Epstein--Bar virus (IgM, EBV-DNA)
Drug-induced liver injury (DILI)
 Thiopurines Thiopurine metabolite levels [6-thioguanine nucleotides (6-TGN) and 6-methylmercaptopurine (6-MMP)]
Nonalcoholic fatty liver disease (NAFLD)
 Hepatic steatosis caused by obesity BMI, ultrasound
 Hepatic steatosis caused by starvation BMI, ultrasound
Biliary obstruction
 Bile stones Ultrasound
 Choledochal malformation Ultrasound
Vascular liver disease
 Portal or hepatic vein thrombosis Doppler-ultrasound
Other
 Celiac disease Celiac antibodies
 Wilson disease Bloodmarkers (ceruloplasmin, free copper, Coomb's test)
Urine (24 h copper excretion)
Liver biopsy (copper content)
Ophthalmologist (Kayser--Fleischer rings)
Genetic testing (ATP7B variants)
 Alpha-1-antitrypsin deficiency Alpha-1-antitrypsin in serum
Alpha-1-antitrypsin phenotyping
Genetic testing (SERPINA1 variants)