Liver function tests (LFTs) are among the most commonly ordered panels in medicine. They help detect liver damage, monitor liver disease, and assess liver function. The key is understanding that LFTs actually measure liver injury (aminotransferases) and bile flow (cholestatic markers) โ not liver function per se. True function tests include albumin, INR, and bilirubin.
ALT (Alanine Aminotransferase)
ALT is the most liver-specific enzyme. It is found predominantly in liver cells and leaks into the bloodstream when hepatocytes (liver cells) are damaged. Normal range: males 7โ56 IU/L, females 7โ45 IU/L. ALT elevation patterns:
- Mild elevation (1โ3ร ULN): fatty liver, medications, thyroid disease
- Moderate elevation (3โ10ร ULN): alcoholic hepatitis, autoimmune hepatitis
- Massive elevation (> 10ร ULN): viral hepatitis, ischaemic hepatitis, drug toxicity
- Isolated ALT > 10ร ULN suggests hepatocellular (cell-damaging) injury
AST (Aspartate Aminotransferase)
AST is less liver-specific than ALT โ it is also found in muscle, heart, and kidneys. The AST:ALT ratio is diagnostically important. A ratio > 2:1 (particularly with AST 2โ6ร normal) strongly suggests alcoholic liver disease. A ratio < 1 (ALT > AST) is more typical of non-alcoholic fatty liver disease (NAFLD). Very high AST in the thousands suggests acute liver cell death (ischaemia, toxin).
ALP and GGT: Cholestatic Markers
Alkaline phosphatase (ALP) and gamma-glutamyl transferase (GGT) are elevated when bile flow is obstructed (cholestasis). ALP is also elevated in bone disease (growing children, Paget's disease, bone metastases). GGT confirms the elevated ALP is from the liver (not bone) and is also a sensitive marker of alcohol use. Normal ALP: 44โ147 IU/L; GGT: males 9โ48 IU/L, females 9โ36 IU/L.
Elevated ALP + elevated GGT โ liver/biliary source. Elevated ALP + normal GGT โ bone source. This distinction guides further investigation (ultrasound vs bone scan).
Bilirubin: The Yellow Pigment
Bilirubin is produced from haemoglobin breakdown. Total bilirubin normal range: 0.1โ1.2 mg/dL (2โ21 ยตmol/L). When elevated, it causes jaundice (yellow skin/eyes). Fractionating into direct (conjugated) and indirect (unconjugated) bilirubin helps identify the cause: high unconjugated bilirubin suggests haemolysis or Gilbert's syndrome; high conjugated bilirubin suggests liver cell disease or bile duct obstruction.
Albumin and INR: True Liver Function
Albumin (normal 3.5โ5.0 g/dL) and INR (normal 0.8โ1.2) measure the liver's synthetic function. Low albumin and elevated INR indicate that the liver has lost significant function โ seen in cirrhosis, acute liver failure, and end-stage disease. These are more concerning than aminotransferase elevations alone.
- Low albumin (< 3.5 g/dL): decreased synthesis or protein loss (nephrotic syndrome)
- Elevated INR (> 1.5): impaired clotting factor production or warfarin therapy
- Combined low albumin + high INR + jaundice = severe hepatic dysfunction
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Dr. Naeem Mahmood Ashraf
PhD Biochemistry & Biotechnology
University of Punjab, Lahore
Dr. Naeem Mahmood Ashraf is a distinguished biochemist and biotechnologist at the University of Punjab, Lahore, Pakistan. With a PhD in Biochemistry & Biotechnology and over 45 peer-reviewed publications (h-index: 10), Dr. Ashraf brings deep expertise in clinical biochemistry, genomics, and computational biology to LabSense AI. His research bridges laboratory science and patient care, ensuring all interpretations follow WHO, IFCC, and AACC international standards.
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