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Real-Time Polymerase Chain Reaction-Based Detection and Quantification of Hepatitis B Virus DNA
Published on: December 15, 2023
Factors influencing clinical course and histological findings in children with chronic hepatitis B
Iwona Mozer-Lisewska1, Anna Mania, Wojciech Słuzewski
1Department of Infectious Diseases and Child Neurology, III Chair of Pediatrics, University of Medical Sciences, Poznañ, Poland. iwonalisewska@poczta.onet.pl
Insights
Pediatric chronic hepatitis B (CHB) shows variable liver injury, with fibrosis progression linked to age at infection. Higher ALT levels indicate significant fibrosis in children with CHB.
Area of Science:
- Pediatric Gastroenterology
- Hepatology
- Virology
Background:
- Chronic hepatitis B (CHB) in children can lead to severe liver disease despite a generally mild course.
- Limited data exists on the clinical outcomes of CHB in pediatric populations.
Purpose of the Study:
- To evaluate inflammatory activity and fibrosis in children with CHB before treatment.
- To correlate these findings with clinical data.
Main Methods:
- Study included 200 children (1.5-18 years) with CHB.
- Histopathological assessment used the modified Knodell system.
- Clinical data and history were analyzed.
Main Results:
- Mild necroinflammatory activity in 115 children, moderate in 44.
- Fibrosis ranged from minimal (S1) to advanced (S3-S4).
- Alanine aminotransferase (ALT) activity correlated with fibrosis stage and was higher in significant fibrosis (S2-S4).
- Spontaneous hepatitis B early antigen seroconversion occurred in 15% and was linked to shorter infection duration and higher ALT.
Conclusions:
- Liver injury in pediatric CHB ranges from minimal to advanced necroinflammation and fibrosis.
- Fibrosis progression appears related to age at infection.
- Higher ALT levels are associated with significant fibrosis in children with CHB.
Introduction:
Although the clinical course of chronic hepatitis B (CHB) is relatively mild in a majority of children, a certain proportion of patients develops chronic liver disease that finally results in serious liver injury. Reports regarding clinical outcome of infection are scarce.
Objective:
The aim of this study was to assess inflammatory activity, fibrosis, and their correlation to clinical data in children with CHB before antiviral treatment.
Materials And Methods:
The study included 200 children, aged 1.5-18 years (mean 7.49+/-4.01 years), with CHB hospitalized before liver biopsy between 1992 and 2003. History and clinical data were analyzed. Histopathological assessment was based on the modified Knodell system. Statistical analysis was performed, and results with P<0.05 were considered significant.
Results:
Necroinflammatory activity was found to be mild in 115 children and moderate in 44. Ninety-three children had minimal fibrosis (S1), 62 children - S2, and the remaining 8 - S3-S4. Alanine aminotransferase (ALT) activity was proportional to staging (Kruskall-Wallis test H=10.84, P=0.028) and was significantly higher in the children with staging >or=S2, P=0.0008. Spontaneous hepatitis B early antigen seroconversion occurred in 30/200 children (15%) and was related to the shorter length of infection, P=0.008.
Conclusion:
Intensity of liver injury in children with CHB varies from minimal to marked necroinflammatory activity and fibrosis varies from none to advanced. Progression of liver fibrosis seems to be proportional to the age at infection. ALT activity appears to be higher in the children with significant (S2-S4) fibrosis. Spontaneous hepatitis B early antigen seroconversion is apparently related to the shorter length of infection and higher ALT activity.
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