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Occult hepatitis B infection in children with chronic liver disease
Anshu Srivastava1, Amrita Mathias, Surender K Yachha
1Departments of aPediatric Gastroenterology bGastroenterology, Sanjay Gandhi Postgraduate Institute of Medical Sciences, Lucknow, Uttar Pradesh, India.
Insights
Occult hepatitis B infection (OBI) is infrequent in Indian children with chronic liver disease (CLD). This study found OBI prevalence similar in cryptogenic and known-etiology CLD, suggesting it may not significantly impact outcomes in this pediatric population.
Area of Science:
- Hepatology
- Pediatric Gastroenterology
- Infectious Diseases
Background:
- Occult hepatitis B infection (OBI) can worsen outcomes in chronic liver disease (CLD).
- Data on OBI in pediatric CLD is lacking.
- This study addresses the prevalence and impact of OBI in HBsAg-negative children with CLD.
Purpose of the Study:
- To determine the prevalence of OBI in HBsAg-negative children with CLD.
- To assess the effect of OBI on disease severity in this population.
- To compare OBI prevalence between cryptogenic CLD and CLD of known etiology.
Main Methods:
- Prospective evaluation of 115 HBsAg-negative CLD children.
- Testing for hepatitis B exposure (total anti-HBc, anti-HBs).
- Hepatitis B virus DNA measurement in anti-HBc positive cases.
Main Results:
- 39.1% of children showed evidence of HBV exposure.
- 4 out of 45 exposed children had seropositive OBI.
- Anti-HBc positive children had higher Child's scores, indicating more severe CLD.
- OBI prevalence was similar in cryptogenic and known-etiology CLD.
Conclusions:
- Seropositive OBI is infrequent in Indian children with CLD.
- The prevalence of OBI is comparable in cryptogenic and known-etiology CLD.
- OBI may not be a significant factor in disease severity in this pediatric group.
Aims:
Occult hepatitis B infection (OBI) may adversely affect the outcome of patients with chronic liver disease (CLD). There are no data on OBI and CLD in children. This study determined the prevalence and effect of OBI in HBsAg-negative CLD children.
Materials And Methods:
CLD children were prospectively evaluated with a demographic, clinical, and investigative proforma. All HBsAg-negative CLD cases were tested for exposure to hepatitis B (total anti-HBc, anti-HBs). Serum hepatitis B virus DNA was measured in exposed (total anti-HBc positive) patients.
Results:
A total of 115 HBsAg-negative CLD children (59 boys, age 9.0±3.6 years) were enrolled. The etiology of CLD was known in 94 cases and 21 children had cryptogenic CLD. Of these, 45 (39.1%) had evidence of HBV exposure (23 total anti-HBc positive, 17 total anti-HBc and anti-HBs positive, five only anti-HBs positive without previous vaccination). The anti-HBc-positive children had a higher Child's score than the anti-HBc-negative children [11 (5-13) vs. 7 (5-13); P=0.00]. A total of 4/45 children had seropositive OBI with serum HBV DNA of 8, 36, 133, and 156 IU/ml, respectively. The proportion of total anti-HBc positivity (8/21 vs. 32/94; P=0.8) and OBI (2/21 vs. 2/94; P=0.1) was similar in cryptogenic CLD and known cause CLD.
Conclusion:
Seropositive OBI is infrequent in Indian children with CLD. The prevalence is similar in cryptogenic and CLD of known etiology.
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