Is Hepatitis B more common in people from Southeast Asia and sub-Saharan Africa?

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Hepatitis B Prevalence in Southeast Asia and Sub-Saharan Africa

Yes, Hepatitis B is significantly more common in people from Southeast Asia and sub-Saharan Africa, where these regions represent the highest endemic areas globally with prevalence rates exceeding 8%. 1

Geographic Distribution and Endemicity

HBV is especially endemic in Asia, the South Pacific Region, and sub-Saharan Africa, where chronic infection rates are substantially higher than in developed nations 1. The epidemiologic data clearly demonstrates:

  • High endemicity regions (>8% prevalence) include most of Asia, sub-Saharan Africa, the South Pacific, and certain indigenous populations in the Arctic 1
  • Sub-Saharan Africa shows particularly high HBsAg prevalence, with some areas reaching 23.5% in certain populations 2
  • Southeast Asia and East Asia maintain prevalence rates of 5-10% in adults with chronic HBV infection 2
  • Approximately 45% of the world's population lives in these high-endemicity regions 3

Transmission Patterns by Region

The mode of HBV transmission differs significantly between these endemic regions and developed countries:

  • In Asia (particularly Southeast and East Asia), perinatal transmission from HBeAg-positive mothers is the predominant route, with 90% risk of chronic infection in newborns 1, 3
  • In sub-Saharan Africa, Alaska, and Mediterranean countries, person-to-person transmission during childhood is more common than perinatal transmission 1
  • These childhood transmission patterns (first 5 years of life) carry a 25-30% risk of developing chronic infection 1, 3

Clinical Significance and Disease Burden

The high prevalence in these regions translates to devastating health consequences:

  • In China and sub-Saharan Africa specifically, HBV-associated hepatocellular carcinoma (HCC) is one of the leading causes of cancer in men 1
  • HBV causes 53% of all hepatocellular carcinoma cases worldwide 3
  • Asia is home to 75% of the world's 400 million HBV carriers 1
  • The prevalence of chronic HBV carriers ranges from 8-20% in Southeast Asia, China, Central Asia, and the Middle East 1

Screening Recommendations

Persons born in hyperendemic areas should be routinely screened for HBV infection, as this population shows 13% HBsAg prevalence and 70-85% prevalence of any HBV serologic markers 1. This screening is critical because:

  • Most infected individuals in these regions acquired HBV perinatally or during early childhood 1
  • The "immune tolerant" phase is prolonged in perinatally-acquired infections, with many patients having high HBV DNA levels but normal ALT 1
  • Early identification allows for appropriate monitoring and treatment to prevent cirrhosis and HCC 1

Important Clinical Caveat

When evaluating patients from Southeast Asia versus sub-Saharan Africa, recognize the different natural history patterns:

  • Southeast Asian patients (particularly those with perinatal transmission) often remain HBeAg-positive longer and may not seroconvert until adulthood 1
  • Sub-Saharan African patients more commonly acquire infection through childhood horizontal transmission, with HBeAg seroconversion typically occurring near or shortly after puberty 1

HIV Co-infection Consideration

Co-infection with HIV is more common in persons from regions where both viruses are endemic, such as sub-Saharan Africa 1. Between 6-13% of HIV-infected persons are co-infected with HBV, and these patients experience higher HBV DNA levels, lower rates of spontaneous HBeAg seroconversion, more severe liver disease, and increased liver-related mortality 1.

References

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Research

Emerging Trends in Epidemiology of Hepatitis B Virus Infection.

Journal of clinical and translational hepatology, 2017

Guideline

Hepatitis B Global Burden and Prevention

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

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