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Published on: May 10, 2022
Clinical features and progression of perinatally acquired hepatitis C virus infection
Massimo Resti1, Paloma Jara, Loreto Hierro
1Department of Paediatrics and Paediatric Hospital A. Meyer, Florence, Italy. m.resti@meyer.it
Insights
Perinatal hepatitis C virus (HCV) infection in children often shows varied ALT levels. While chronic progression is common, liver disease is typically mild, with high early ALT offering a better chance for viral clearance.
Area of Science:
- Pediatrics
- Hepatology
- Infectious Diseases
Background:
- Perinatal transmission of hepatitis C virus (HCV) is a significant concern.
- Understanding the clinical course of vertically acquired HCV infection is crucial for management.
Purpose of the Study:
- To describe the clinical features and disease progression of perinatal hepatitis C virus infection in children.
- To identify factors influencing the outcome of vertically transmitted HCV.
Main Methods:
- Prospective-retrospective study of 70 infants born to HCV-infected mothers.
- Enrollment criteria included HCV RNA or anti-HCV positivity in the first 18 months.
- Follow-up extended to at least 24 months, with clinical and biochemical assessments.
Main Results:
- 93% of infants exhibited elevated ALT levels within the first year.
- 19% achieved sustained ALT normalization and HCV RNA loss by 30 months.
- 81% cumulative probability of chronic HCV progression, generally with mild liver disease.
- Higher initial ALT peaks and HCV genotype 3 were associated with different outcomes.
Conclusions:
- Early perinatal HCV infection presents with diverse ALT abnormalities, influenced by host and viral factors.
- The rate of chronic HCV progression is high, but liver disease severity is usually mild.
- Elevated ALT levels early in infection may predict a better chance of biochemical remission and viral clearance.
Abstract:
The purpose of this prospective-retrospective study was to provide information about the clinical features and progression of hepatitis C virus (HCV) infection transmitted perinatally. Seventy children born to HCV infected woman were enrolled consecutively in five European centers between 1990 and 1999, provided they had HCV RNA in the serum during the first year of life and/or were still anti-HCV positive at 18 months. Sixty-two infants were followed up to 24 months of age or more (range, 24 months-11 years; average, 4.8 +/- 2.3 years). A wide range of ALT elevation was observed in 93% of the infants in the first year of life. During the follow-up, a sustained ALT normalization with loss of HCV RNA was seen in 12/62 (19%) of the children within 30 months of life; 66% of the infants had developed an ALT peak greater than 5x normal at onset (vs. 28% of children with persistent viremia; P < 0.05), and 50% had HCV genotype 3 (vs. 17% of viremic children). Conversely the cumulative probability of chronic progression was 81%. Chronic infection was asymptomatic and liver disease was mild in all 11 children who underwent a biopsy. In conclusion the early stage of acquired perinatally HCV infection is characterized by a wide range of ALT abnormalities, suggesting the interaction of multiple host and virus factors. The chronic progression rate of infection is high, but the associated liver disease is usually mild. High ALT levels at onset seem to offer greater opportunity of biochemical remission and loss of viremia during follow-up.
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