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Published on: May 10, 2022
When does mother to child transmission of hepatitis C virus occur?
1Paediatric HIV Service, Royal Hospital for Sick Children, Edinburgh, Scotland, UK.
Insights
Hepatitis C virus (HCV) infection in children often occurs before birth. Postpartum transmission is rare, but further research into HCV genotypes and infection timing is needed.
Area of Science:
- Virology
- Infectious Diseases
- Pediatrics
Background:
- Hepatitis C virus (HCV) poses a significant global health challenge.
- Understanding mother-to-child transmission (MTCT) is crucial for prevention strategies.
Purpose of the Study:
- To determine the timing of perinatal HCV infection.
- To identify factors associated with mother-to-child transmission of HCV.
Main Methods:
- Prospective cohort study involving 54 HCV-infected children and their mothers.
- Hepatitis C virus RNA polymerase chain reaction (PCR) testing at birth and follow-up.
- Analysis of potential risk factors including infant sex, delivery mode, birth weight, and HCV genotype.
Main Results:
- Approximately 31% of infants showed evidence of intrauterine HCV infection within 3 days of birth.
- Intrauterine infection was associated with lower birth weight and HCV genotype 1.
- Late-onset infection (after 3 days) was observed in 68% of infants, with most cases identified by 3 months.
Conclusions:
- At least one-third of perinatal HCV infections are acquired in utero.
- Postpartum HCV transmission appears to be uncommon.
- Further investigation into the role of HCV genotypes in transmission timing and mechanisms is warranted.
Objective:
To investigate when hepatitis C virus (HCV) infection from mother to child occurs, and evaluate possible associated factors.
Design:
Prospective cohort study.
Patients:
Fifty four HCV infected children tested within three days of birth and their mothers.
Main Outcome Measures:
HCV RNA polymerase chain reaction (PCR) results.
Results:
Seventeen of the children (31%, 95% confidence interval 19% to 46%) were positive in the first 3 days of life and could be assumed to have acquired infection in utero. Testing PCR positive was not associated with sex (53% v 49% boys; p=0.77) or mode of delivery (29% elective caesarean section in both groups; p=0.98). Children with evidence of intrauterine infection were significantly more likely to be of lower birth weight and infected with genotype 1 (58% v 12%, p=0.01). Although a higher proportion of infants born to HCV/HIV co-infected women were PCR positive in the first 3 days of life, this difference did not reach statistical significance; excluding infants born to co-infected women did not affect the results. Thirty seven of the children (68%) were negative in the first 3 days of life, 27 of whom were positive when tested again at 3 months, and nine were first PCR positive after 3 months (one child had no further tests).
Conclusions:
These results suggest that at least one third and up to a half of infected children acquired infection in utero. Although postpartum transmission cannot be excluded, these data suggest that it is rare. The role of HCV genotypes in the timing and mechanism of infection should be explored further.
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