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Aspartate Aminotransferase (AST/SGOT)

Code:8031|CPT:84450|LOINC:1920-8

Synonyms
Глютамин-щавелевоуксусная трансаминаза в сывороткеглутамат-оксалоацетат-трансаминаза сыворотки крови (СГОТ)аспартаттрансаминазасоотношение АСТ/АЛТ.AST/ALT ratioAspartate aminotransferaseAspartate transaminaseSGOTSerum Glutamic Oxaloacetic TransaminaseTransaminases
IncludesAST (SGOT)

Analysis details

Methodology

  • Kinetic method
  • Ultraviolet kinetic (UV) method

Expected Turnaround Time

1 day

Special Instructions

  • Do not eat for 12 hours before the blood draw.
  • Avoid strenuous activity and emotional stress for at least 30 minutes before collection.
  • Do not smoke during the 30 minutes prior to collection.

How to use

The Aspartate Aminotransferase (AST/SGOT) test is used to identify and assess hepatocellular injury and to monitor disease activity and treatment response in liver disorders. Results are interpreted with ALT, alkaline phosphatase, bilirubin, and related tests to differentiate hepatocellular from cholestatic patterns; the AST to ALT ratio can aid evaluation of alcohol-associated liver disease. AST (aspartate transaminase; Serum Glutamic Oxaloacetic Transaminase) may also rise with cardiac or skeletal muscle injury, including myocardial infarction, myositis, and muscular dystrophies, as well as during systemic inflammatory or ischemic states. Accordingly, interpretation relies on clinical context and, when appropriate, complementary cardiac and muscle biomarkers.

Limitations

AST is distributed widely across tissues, with highest activity in liver and heart and comparatively lower activity in kidney and skeletal muscle. Serum AST increases with hepatocellular injury and with muscle injury, so it is commonly included in liver test panels but is not liver-specific. Clinical interpretation requires integration with ALT, alkaline phosphatase, bilirubin, and the physical examination, and, when indicated, with cardiac and muscle biomarkers. Marked elevations are typical of acute hepatocellular injury, whereas extrahepatic processes such as myocardial infarction and myopathies can also produce elevated AST.

UnitIU/L
Reference interval
AgeMaleFemale
≤28d2575
1mo–12mo1560
1y–122y0–500–35
IndicationsWorkup of jaundice, dark urine (choluria), pale or acholic stools, or generalized pruritus, Right upper quadrant abdominal pain or abdominal distension, Anorexia, nausea, or vomiting raising concern for hepatic disease, Unexplained fatigue or asthenia when liver dysfunction is suspected, History of viral hepatitis or recent exposure to hepatitis viruses, Heavy alcohol consumption or alcohol use disorder, Use of medications with hepatotoxic potential, Family history suggestive of liver disease, Presence of metabolic syndrome or diabetes mellitus, Monitoring response to therapy for established liver disease

Possible Causes of Abnormal Results

Increased levels

  • acetaminophen
  • alcoholic hepatitis
  • anabolic-androgenic steroids
  • carbon tetrachloride
  • central nervous system diseases
  • cholecystitis
  • chronic alcohol ingestion
  • cirrhosis
  • congestive heart failure
  • dermatomyositis
  • duchenne muscular dystrophy
  • erythromycin
  • gangrene
  • hemochromatosis
  • hemolytic anemia
  • hepatitis
  • hypothyroidism
  • indomethacin
  • infectious mononucleosis
  • isoniazid
  • large necrotic tumors
  • legionnaires' disease
  • macro-ast
  • methyldopa
  • myocardial infarction
  • myocarditis
  • opiates
  • pancreatitis
  • pericarditis
  • phenothiazines
  • polymyositis
  • progesterone
  • renal infarction
  • reye syndrome
  • salicylates
  • shock
  • surgery
  • trauma
  • trichinosis

Decreased levels

  • metronidazole
  • trifluoperazine
  • uremia
  • vitamin b6 deficiency

Specimen Requirements

SpecimenSerum
ContainerGold/Tiger Top (SST, Gel Separator)
Volume1 mL (min 0.7 mL)
Storage InstructionsRoom temperature, Refrigerated, Frozen

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