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Published on: October 13, 2018
Association of Rotavirus Infection With Biliary Atresia: A Retrospective Comparative Analysis of Virus-Specific
Yoshiki Kawamura1, Masaru Ihira2, Yuki Higashimoto3
1Department of Pediatrics, Fujita health University School of Medicine, Toyoake, Japan.
Insights
Infants with biliary atresia (BA) show higher rotavirus (RV) immunoglobulin A (IgA) levels, suggesting a potential link between RV infection and BA. Further research is needed to confirm this association and its implications for infant health.
Area of Science:
- Hepatology
- Pediatric Gastroenterology
- Infectious Diseases
Background:
- Biliary atresia (BA) is a severe infantile liver disease with unknown causes.
- Rotavirus (RV) infection is suspected in BA pathogenesis, but human evidence is limited.
- This study examines serological markers of recent RV infection in infants with BA.
Purpose of the Study:
- To investigate the association between rotavirus (RV) infection and biliary atresia (BA) in infants.
- To assess the presence of RV-specific immunoglobulin A (IgA) as a marker of primary RV infection.
- To compare RV-IgA levels in infants with BA versus healthy controls.
Main Methods:
- Retrospective analysis of serum samples from 17 infants with BA and 30 controls.
- Enzyme-linked immunosorbent assay (ELISA) to detect anti-RV-IgA titers.
- Commercial immunoassays for Cytomegalovirus (CMV)-IgM and Epstein-Barr virus (EBV)-VCA-IgM.
Main Results:
- RV-IgA was detected in 70.6% of BA patients vs. 3.4% of controls (p < 0.001).
- Significantly higher RV-IgA titers were observed in the BA group compared to controls (p = 0.004).
- 84.6% of BA patients diagnosed after 14 days of age were RV-IgA-positive.
Conclusions:
- Findings suggest a potential association between rotavirus infection and biliary atresia pathogenesis.
- The lack of BA reduction post-RV vaccine introduction necessitates cautious interpretation.
- Prospective multicenter studies are required to establish a causal role for RV in BA.
Background:
Biliary atresia (BA) is a severe infantile hepatobiliary disorder of unknown etiology. Perinatal rotavirus (RV) infection has been implicated in animal models of BA; however, supporting human data remains limited. The study investigated the serological evidence of recent RV infection in infants with BA using RV-specific immunoglobulin (Ig)-A, a marker of primary infection unaffected by maternal antibodies.
Methods:
Serum samples from 17 infants with BA and 30 age-matched controls without gastrointestinal symptoms or prior RV vaccination were retrospectively analyzed. Anti-RV-IgA titers were measured by enzyme-linked immunosorbent assay using purified WA-strain virions. Cytomegalovirus (CMV)-IgM and Epstein-Barr virus (EBV)-viral capsid antigen (VCA)-IgM levels were assessed using commercial enzyme immunoassays.
Results:
RV-IgA was detected in 70.6% (12/17) of the patients with BA versus 3.4% (1/29) of the controls (p < 0.001). RV-IgA titers were significantly higher in the BA group (median: interquartile range 28.0:26.0-210.0) than in the control group (23.5:22.0-24.8) (p = 0.004). Among patients diagnosed with BA after 14 days of age, 84.6% (11/13) were RV-IgA-positive. CMV-IgM was detected in three patients in the BA group and one individual in the control group, while EBV-VCA-IgM was negative in BA patients and positive in two controls; neither difference was statistically significant.
Conclusions:
The study findings support the potential association between RV infection and BA pathogenesis. However, the lack of an epidemiological reduction in BA following the introduction of the RV vaccine warrants caution in other studies. Further prospective multicenter studies are required to elucidate the causal role of RV infection in BA development.
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