Atlas
Hepatic panel

Alanine aminotransferaseALT

Liver-specific aminotransferase; the most useful single marker of hepatocyte injury.

Sample
Serum
Clinical reference range
7 to 35 U/L
Adult male
Conv: 735 U/LFunc: 1025 U/L
Biology

What it measures

Catalyzes alanine + α-KG ↔ pyruvate + glutamate. Highly concentrated in hepatocytes; cytoplasmic. Half-life ~47 h.

Clinical use

Why we order it

Detect and monitor hepatocellular injury, screen for NAFLD.

Lens · Clinical

Interpretation by lens

Clinical interpretation

Persistent ALT elevation >6 months warrants full chronic-liver-disease workup including viral serologies, autoimmune markers, ferritin, ceruloplasmin, alpha-1 antitrypsin, and ultrasound.

Functional interpretation

Functional optimal <25 U/L; values 25–40 are common in early NAFLD that mainstream cutoffs miss.

Research note

AASLD 2023 NAFLD/MASLD guidelines lowered diagnostic thresholds and emphasize FIB-4 + elastography over ALT alone.

Differential

Causes of abnormal values

Causes of HIGH
  • NAFLD/MASLD (most common worldwide)
  • Alcohol (typically AST > ALT)
  • Viral hepatitis A/B/C
  • Drug-induced liver injury (acetaminophen, statins, methotrexate, isoniazid)
  • Autoimmune hepatitis
  • Hemochromatosis, Wilson's, α1-antitrypsin
  • Celiac disease
  • Skeletal muscle injury (less than AST)
Causes of LOW
  • Vitamin B6 deficiency (cofactor)
  • Chronic kidney disease
Pitfalls

Pre-analytic & interpretation traps

  • !ALT 'upper normal' (35–40 U/L) is too lenient — modern thresholds are <30 (men) and <19 (women).
  • !Normal ALT does not exclude advanced NAFLD with fibrosis.
Follow-up orders

Logical next-step labs

Evidence-graded claims

What the data says

B
Lower upper-normal ALT thresholds (<30M/<19F) catch more clinically relevant disease
Prati 2002 and AASLD support.
A
Statin-induced ALT elevations <3× ULN do not require statin discontinuation
FDA and major lipid guidelines.
Related

Related biomarkers