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Author Spotlight: Advancements and Challenges in Hepatitis B Virus Detection
Published on: December 15, 2023
Cohort study of familial viral hepatitis and risks of paediatric cancers
Julia E Heck1,2, Chia-Kai Wu3, Xiwen Huang2
1Department of Rehabilitation and Health Services, College of Health and Public Service, University of North Texas, Denton, TX, USA.
Insights
Parental hepatitis B (HBV) and C (HCV) infections are linked to increased risks of certain childhood cancers, including hepatoblastoma and non-Hodgkin lymphoma. Screening and antiviral treatment for parents could potentially prevent paediatric cancers.
Area of Science:
- Epidemiology
- Oncology
- Virology
Background:
- Viral hepatitis, including hepatitis B (HBV) and C (HCV), is a known cause of adult cancers.
- Limited epidemiologic data exists on the association between parental viral hepatitis and paediatric cancer risks.
- This study investigates the link between parental HBV and HCV infections and cancer development in offspring.
Purpose of the Study:
- To examine the association between parental hepatitis B (HBV) and C (HCV) infections and the risk of various cancers in children.
- To assess the potential role of parental viral hepatitis as a risk factor for paediatric cancers.
- To provide evidence for potential cancer prevention strategies through parental screening and treatment.
Main Methods:
- A nationwide cohort study in Taiwan (2,079,037 children, 2160 cancer cases) using Cox proportional-hazard regressions.
- Validation of findings in a separate population-based case-control study in Denmark (6422 cases, 160,522 controls).
- Ascertainment of cancer cases through national cancer registries.
Main Results:
- Paternal HBV infection was associated with an increased risk of childhood hepatoblastoma (HR=1.77, 95% CI=1.05-2.97).
- Paternal HCV infection showed a significant association with childhood non-Hodgkin lymphoma (HR=2.06, 95% CI=1.13-3.74).
- Maternal HCV infection demonstrated a weak association with an increased risk of all childhood cancers combined (HR=1.45, 95% CI=0.95-2.22).
Conclusions:
- Parental HBV and HCV infections may represent risk factors for both hepatic and non-hepatic cancers in children.
- If causal, parental screening and antiviral therapy could be strategies to prevent certain paediatric cancers.
- Further research is warranted to confirm causality and explore intervention effectiveness.
Background:
Although viral hepatitis causes paediatric hepatocellular carcinoma and hepatic and extrahepatic cancers in adults, there are few epidemiologic studies on paediatric-cancer risks from parental viral hepatitis. In a nationwide study in a viral hepatitis endemic region and with confirmation in another population-based sample, we examined associations between parental hepatitis B (HBV) and C (HCV) infections and risks of cancers in offspring.
Methods:
We included all children born in Taiwan in 2004-2014 (N = 2 079 037) with 2160 cancer cases ascertained from the Cancer Registry. We estimated risks for paediatric cancers using Cox proportional-hazard regressions. We checked these associations in a nationwide case-control study in Denmark (6422 cases, 160 522 controls).
Results:
In Taiwan, paternal HBV was related to child's hepatoblastoma [hazard ratio (HR) = 1.77, 95% confidence interval (CI) = 1.05, 2.97] when identified at any time in the medical record, and when analyses were limited to hepatitis diagnoses occurring before the child's birth, risks increased (HR = 2.08, 95% CI = 1.13-3.80). Paternal HCV was related to child's non-Hodgkin lymphoma (HR = 2.06, 95% CI = 1.13-3.74). Maternal HCV was weakly related to increased risks of all childhood cancers [all types combined; HR = 1.45, 95% CI = 0.95-2.22]. The population-attributable fraction of hepatoblastoma for maternal, paternal and child HBV was 2.6%, 6.8% and 2.8%, respectively.
Conclusions:
Parental HBV and HCV may be risk factors for hepatic and non-hepatic cancers in children. If associations are causal, then parental screening and treatment with antivirals may prevent some paediatric cancers.
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