Interpreting Liver function tests (LFTs)

Components of the LFT panel

  • ALT (alanine aminotransferase): Marker of hepatocellular injury.
  • AST (aspartate aminotransferase): Less specific; can be elevated in muscle injury.
  • ALP (alkaline phosphatase): Raised in cholestasis; also found in bone.
  • GGT (gamma-glutamyl transferase): Helps confirm hepatic source of raised ALP.
  • Bilirubin: Elevated in hepatocellular injury or cholestasis.
  • Albumin: Low in chronic liver disease or systemic illness.
  • Prothrombin time (PT)/INR: May be included; prolonged in synthetic failure.

Initial pattern recognition

  • Hepatocellular (↑ ALT/AST): Viral hepatitis, NAFLD, drug-induced liver injury, alcohol.
  • Cholestatic (↑ ALP ± GGT): Gallstones, biliary obstruction, PBC, PSC.
  • Isolated hyperbilirubinaemia: Consider Gilbert’s syndrome if unconjugated.
  • Hypoalbuminaemia: Consider chronic liver disease, nephrotic syndrome, malnutrition.

Common scenarios in primary care

  • Isolated mildly raised ALT: Check alcohol use, BMI, metabolic syndrome. Consider NAFLD.
  • Raised ALP with normal GGT: Suggests non-hepatic cause, e.g. bone disease.
  • Raised ALP and GGT: Suggests biliary disease—consider USS liver and referral if persistent.
  • Persistent abnormal LFTs >3 months: Refer for imaging and hepatology work-up (BSG 2017).
visual summary of LFTs pathway
Reproduced from : https://gps.northcentrallondon.icb.nhs.uk/pathways/ncl-adult-abnormal-liver-function-tests-primary-care-clinical-pathway