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[Serum gamma-glutamyl transpeptidase activity in children with chronic hepatitis B]
Dariusz Marek Lebensztejn1, Elzbieta Skiba, Maria Elzbieta Sobaniec-Lotowska
1III Klinika Chorób Dzieci Akademii Medycznej w Białymstoku. DariuszMar.8810735@pharmanet.com.pl
Insights
Gamma-glutamyl transferase (GGT) can predict advanced liver fibrosis in children with chronic hepatitis B. This enzyme shows potential as a non-invasive marker for fibrosis assessment in pediatric patients.
Area of Science:
- Hepatology
- Biochemistry
- Pediatric Gastroenterology
Context:
- Chronic hepatitis B infection in children can lead to liver fibrosis.
- Accurate assessment of fibrosis is crucial for guiding treatment decisions.
- Non-invasive biomarkers are needed to complement liver biopsy.
Purpose:
- To evaluate serum enzyme activities (ALT, AST, GGT, ALP) for assessing liver fibrosis in children with chronic hepatitis B.
- To determine the utility of GGT in predicting advanced fibrosis.
Summary:
- Serum GGT activity was measured in 47 children (aged 4-16) with biopsy-proven chronic hepatitis B before interferon alpha treatment.
- Receiver operating characteristics (ROC) analysis indicated that a GGT level of 19 IU/l had 50% sensitivity and 90% specificity for advanced fibrosis (Batts and Ludwig score =3).
- Other tested enzymes (ALT, AST, ALP) did not show significant predictive power for advanced fibrosis.
Impact:
- Gamma-glutamyl transferase (GGT) is identified as a suitable serum marker for predicting advanced liver fibrosis in pediatric patients with chronic hepatitis B.
- This finding may facilitate earlier detection and management of liver fibrosis in children.
- Highlights the potential of GGT as a non-invasive tool in pediatric hepatology.
Unlabelled:
THE AIM OF THE STUDY was evaluation of serum activity of chosen enzymes (ALT, AST, GGT and ALP) in assessment of fibrosis degree in children with chronic hepatitis B.
Material And Methods:
We determined serum activity of liver enzymes in 47 children aged 4-16 with biopsy-verified chronic hepatitis B, prior to interferon alpha treatment. Fibrosis stage was assessed in a blinded fashion according to Batts and Ludwig. We defined advanced fibrosis as a score =3. Receiver operating characteristics (ROC) analysis was used to calculate the power of the assays to detect advanced liver fibrosis (AccuROC, Canada).
Results:
Serum GGT activity of 19 IU/I had a sensitivity of 50% and a specificity of 90% (AUC=0.7324, p=0.0391) to predict advanced fibrosis. All other enzymes did not allow a useful prediction.
Conclusion:
GGT is suitable serum marker to predict advanced liver fibrosis in children with chronic hepatitis B.
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