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Published on: June 5, 2020
Sexual Dimorphism in Chronic Hepatitis B Virus (HBV) Infection: Evidence to Inform Elimination Efforts
Robin Brown1, Philip Goulder2, Philippa C Matthews1,3,4,5
1Harris Manchester College, University of Oxford, Oxford, Oxon, OX1 3TD, UK.
Insights
Males face higher risks for hepatitis B virus (HBV) infection, chronic outcomes, and complications like liver cancer compared to females. Understanding sexual dimorphism is key to improving HBV prevention and treatment strategies.
Area of Science:
- Hepatology
- Immunology
- Infectious Diseases
Background:
- Hepatitis B virus (HBV) infection affects nearly 300 million people globally, causing significant mortality and morbidity.
- Sexual dimorphism, differences in disease susceptibility and outcomes between sexes, is evident in HBV infection.
Purpose of the Study:
- To review the mechanisms, outcomes, and impact of sexual dimorphism in HBV infection.
- To explore how insights into sexual dimorphism can advance HBV surveillance, treatment, and prevention.
Main Methods:
- Assimilation of human and animal data.
- Review of existing literature on sexual dimorphism in HBV.
Main Results:
- Males exhibit higher susceptibility to HBV exposure, chronic infection, and severe complications such as cirrhosis and hepatocellular carcinoma (HCC).
- Differential immune responses, liver sexual dimorphism, and androgenic influences on the HBV genome contribute to varied outcomes.
- Age and gender-related factors significantly modulate the impact of sexual dimorphism in HBV infection and healthcare engagement.
Conclusions:
- Sexual dimorphism profoundly influences HBV infection dynamics and clinical outcomes.
- Further research into sexual dimorphism can inform targeted interventions for HBV elimination.
- Translational application of these findings is crucial for advancing public health strategies against HBV.
Abstract:
Sexual dimorphism in infectious diseases refers to the different infection susceptibilities and outcomes between males and females, and has been described for many pathogens, including hepatitis B virus (HBV). HBV is a substantial global health problem, with close to 300 million people chronically infected, and accounting for a million deaths each year, with an urgent need for enhanced interventions to support progress towards elimination goals. Sexual dimorphism has a strong influence in HBV infection, with males more likely to be exposed, to develop chronic infection, and to suffer from complications including cirrhosis and hepatocellular carcinoma (HCC) compared to females. Different outcomes are driven by differential immune responses, sexual dimorphism of the liver, and androgen response elements in the HBV genome. The impact of sex may also vary with age, with changes at puberty and influences of menarche, pregnancy and menopause in females. In addition, gender has complex influences on education, beliefs, behaviour and access to / engagement with healthcare services, which may contribute to differences in diagnosis and treatment. Interplay between these complex factors, alongside other attributes of host, virus and the environment, accounts for different outcomes of infection. However, gaps remain in our understanding of sexual dimorphism in HBV, and little effort has previously been made to harness this knowledge for translational gains. In this review, we assimilate human and animal data to consider the mechanism, outcomes and impact of sexual dimorphism, and consider how these insights can be used to inform advances in surveillance, treatment and prevention for HBV infection.
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