γ-Glutamyl Transferase (GGT)
Code:8033|CPT:82977|LOINC:2324-2
| Includes | GGT |
|---|
Analysis details
Methodology
- Kinetic method
- Kinetic colorimetric method
Expected Turnaround Time
1 day
Special Instructions
- Do not eat or drink anything except water for at least 12 hours before the blood draw.
- For 30 minutes before collection, avoid vigorous exercise, emotional stress, and smoking.
How to use
Gamma‑glutamyl transferase (GGT), also known as gamma‑glutamyl transpeptidase or Gamma GT, is used to assess hepatobiliary disease, especially obstructive jaundice and intrahepatic cholestasis, where GGT often responds more than AST or ALT. When alkaline phosphatase is increased, concurrent GGT helps determine whether the source is hepatic versus bone. The assay supports evaluation of primary biliary cholangitis, primary sclerosing cholangitis, pancreatitis, and malignancy affecting the liver or pancreas. GGT is used to monitor alcohol‑related liver disease and to follow patients over time to distinguish abstinence from relapse. Markedly increased activities may occur in biliary atresia and in primary biliary cholangitis. GGT may be increased with hyperthyroidism and decreased with hypothyroidism.
Limitations
Bile produced by hepatocytes flows through canaliculi into the biliary tree and onward to the intestine. Gamma‑glutamyl transferase, a membrane enzyme of hepatocytes and the biliary epithelium, appears in serum when cholestatic injury disrupts these structures and increases canalicular enzyme release. GGT is highly sensitive for cholestasis and can precede alkaline phosphatase increases, but it lacks specificity because activities rise in a wide range of hepatic and pancreatic disorders and the enzyme is also present in kidney, spleen, pancreas, brain, and prostate. A pattern of elevated alkaline phosphatase with normal GGT does not reliably exclude liver disease, and GGT has limited utility as a stand‑alone tumor marker in malignancy evaluations.
| Unit | IU/L | ||||
|---|---|---|---|---|---|
| Reference interval |
| ||||
| Indications | Inclusion in general health screening or preoperative laboratory panels, Use as part of a liver function assessment, Workup of cholestatic or hepatocellular presentations, including right upper quadrant pain; cholestatic jaundice; dark urine; pale (acholic) stools; pruritus; fatigue; anorexia; nausea; or vomiting, Concern for alcohol use disorder, and monitoring during therapy for alcoholism or alcoholic hepatitis |
Possible Causes of Abnormal Results
Increased levels
- acetaminophen
- antibiotics
- antidepressants
- antifungals
- aspirin
- fenobarbital
- h2-receptor antagonists
- obesity
- oral contraceptives
- statins
- testosterone
Decreased levels
- ascorbic acid (vitamin c)
Specimen Requirements
| Specimen | Serum |
|---|---|
| Container | Gold/Tiger Top (SST, Gel Separator) |
| Volume | 1 mL (min 0.7 mL) |
| Storage Instructions | Room temperature, Refrigerated, Frozen |