Alanine Aminotransferase (ALT/SGPT)
Code:8030|CPT:84460|LOINC:1742-6
| Includes | ALT (SGPT) |
|---|
Analysis details
Methodology
- Kinetic method
- Ultraviolet kinetic (UV) method
Expected Turnaround Time
1 day
Special Instructions
- Fast for 12 hours before the blood draw.
- For 30 minutes before collection, avoid vigorous physical activity and minimize emotional stress.
- Do not smoke during the 30 minutes preceding specimen collection.
How to use
Alanine aminotransferase (ALT), also known as alanine transaminase or serum glutamic-pyruvic transaminase (SGPT), is used to detect and follow hepatocellular injury, including viral hepatitis and toxic or drug-induced hepatitis, and to aid in the assessment of cirrhosis and other liver disorders. ALT is commonly ordered with AST; the magnitude and pattern of ALT and AST elevations, and their ratio, can support differential diagnosis. In suspected acute hepatitis A or B and in hepatitis C, serologic assays establish the specific etiology. Persistent absence of viral hepatitis markers in the setting of hepatitic enzyme elevations may suggest drug-induced hepatitis that improves after the agent is withdrawn. ALT can also increase with infectious mononucleosis and may be elevated in heart failure.
Limitations
ALT resides predominantly within hepatocytes. Hepatocellular injury increases membrane permeability or causes cell necrosis, permitting ALT to enter the circulation—often preceding clinical manifestations such as jaundice. ALT and AST are core components of routine liver panels; compared with AST, ALT is generally more specific for hepatocellular injury. When interpreted together, the AST/ALT ratio can help suggest potential etiologies of liver disease. Although ALT is primarily hepatic, elevations can occur with extrahepatic conditions, including disorders of skeletal muscle.
| Unit | IU/L | |||||||||
|---|---|---|---|---|---|---|---|---|---|---|
| Reference interval |
| |||||||||
| Indications | Assessment of possible liver disease in patients reporting fatigue or asthenia, Loss of appetite (anorexia), Nausea and vomiting, Abdominal pain or progressive abdominal distention, New or worsening jaundice (icterus), Dark (“tea-colored”) urine or pale/acholic stools, Generalized pruritus, Prior viral hepatitis or recent exposure to hepatitis viruses, Heavy alcohol consumption or alcohol use disorder, Family history of liver disease, Use of medications or substances with hepatotoxic potential, Obesity, metabolic syndrome, or diabetes mellitus, Monitoring of liver disease during treatment |
Possible Causes of Abnormal Results
Increased levels
- dermatomyositis
- hemolysis
- obesity
- polymyositis
- rhabdomyolysis
- skeletal muscle injury
Specimen Requirements
| Specimen | Serum |
|---|---|
| Container | Gold/Tiger Top (SST, Gel Separator) |
| Volume | 1 mL (min 0.7 mL) |
| Storage Instructions | Room temperature, Refrigerated |
References
Tonks DB. A study of the accuracy and precision of clinical chemistry determinations in 170 Canadian laboratories. Clin Chem. 1963 Apr; 9:217-233. PubMed 13985504