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Correlation Between Clinical Indicators and Liver Pathology in Children with Chronic Hepatitis B
Chenyang Huang1,2, Ying Lu3, Ziwei Wang2
1Medical School of Chinese PLA, Beijing 100853, China.
Insights
Monitoring age, ALT, AST, and GGT levels helps identify children with chronic hepatitis B (CHB) at risk for liver inflammation and fibrosis. Early detection through these markers aids in managing pediatric liver disease.
Area of Science:
- Hepatology
- Pediatric Gastroenterology
- Viral Hepatitis Research
Background:
- Chronic hepatitis B (CHB) poses a significant global health challenge in children.
- Liver inflammation and fibrosis are key concerns impacting disease progression and long-term outcomes in pediatric CHB.
- Accurate assessment of liver pathology is crucial for effective management.
Purpose of the Study:
- To evaluate the predictive value of clinical indicators for liver inflammation and fibrosis severity in pediatric CHB patients.
- To identify key biochemical markers and age as predictors of liver pathology in children with CHB.
- To inform the development of non-invasive diagnostic algorithms for pediatric liver disease.
Main Methods:
- Retrospective analysis of 1629 pediatric CHB patients (2000-2021).
- Liver biopsies assessed using the Scheuer scoring system for inflammation and fibrosis.
- Restricted cubic spline regression models used to analyze associations between age, ALT, AST, GGT, and liver pathology.
Main Results:
- Older age correlated with increased risk of moderate-to-severe inflammation (OR 2.21) and significant fibrosis (OR 2.22).
- Elevated ALT (≥80 U/L) linked to higher likelihood of moderate-to-severe inflammation (OR 1.82).
- Higher GGT (≥50 U/L) significantly associated with advanced fibrosis (OR 2.62).
Conclusions:
- Regular monitoring of ALT, AST, and GGT levels is vital for identifying pediatric CHB patients at high risk.
- Age and biochemical markers (ALT, GGT) are valuable predictors of liver inflammation and fibrosis severity.
- Integrating these factors into non-invasive algorithms can improve early detection and management of pediatric liver pathology.
Abstract:
Background: Chronic hepatitis B (CHB) in children presents a significant global health challenge, with liver inflammation and fibrosis being critical concerns for disease progression and long-term outcomes. Methods: This retrospective study analyzed 1629 pediatric CHB patients from the Fifth Medical Center of Chinese PLA General Hospital, spanning from January 2000 to December 2021. Liver biopsies were performed to assess the severity of liver inflammation and fibrosis, which were graded using the Scheuer scoring system. Key clinical indicators, including age, alanine aminotransferase (ALT), aspartate aminotransferase (AST), and gamma-glutamyl transferase (GGT), were evaluated for their predictive value in determining disease severity using restricted cubic spline regression models. Results: Significant nonlinear associations were found between the clinical indicators and liver pathology. Older age was strongly associated with increased risks of moderate to severe inflammation (OR 2.21, 95% CI: 1.34-3.63, p = 0.002) and significant fibrosis (OR 2.22, 95% CI: 1.31-3.77, p = 0.003). Elevated ALT levels (≥80 U/L) were correlated with a higher likelihood of moderate to severe inflammation (OR 1.82, 95% CI: 1.05-3.15, p = 0.033), while higher GGT levels (≥50 U/L) were significantly associated with advanced fibrosis (OR 2.62, 95% CI: 1.72-3.99, p < 0.001). Conclusions: Regular monitoring of clinical indicators such as ALT, AST, and GGT levels plays a critical role in identifying pediatric CHB patients at higher risk of moderate to severe inflammation and significant fibrosis. Our findings highlight the value of integrating age and key biochemical markers into non-invasive diagnostic algorithms for the early detection and management of liver pathology in children.
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