Understanding Hepatitis B in Eritrea A Deep Dive into Virological and Serological Markers

Introduction

Background of the Study

The study highlights that chronic hepatitis B virus (HBV) infection affects a significant proportion of the Eritrean population, with transmission primarily through early childhood exposure. A notable finding was the high prevalence of HBeAg-negative patients—a marker indicating a less active phase of HBV replication, which can still pose long-term risks if undetected.

Key highlights include:

  • 305 patients were studied from hospitals across Asmara, Eritrea.
  • Mean patient age was 41.3 years, with 71.5% being male.
  • Majority had normal liver enzyme levels, suggesting an inactive carrier state.

Serological and Virological Findings

  • HBsAg-positive patients: 293 out of 305.
  • Anti-HBc antibodies were present in 98.4% of cases, indicating prior or ongoing infection.
  • Only 6.8% of patients were HBeAg-positive, while 82.6% were anti-HBe positive.
  • A substantial number (41.6%) showed detectable HBV DNA, but only 22.86% had high-level replication (>2,000 IU/mL).

This indicates that a majority of patients are in the “low replicative phase” — a relatively stable stage of infection.

Broader Medical Perspectiv

The World Health Organization (WHO) identifies hepatitis B as one of the deadliest but preventable infections. Screening strategies involving HBsAg, anti-HBc, and anti-HBs markers remain the gold standard for identifying chronic infection or past exposure.
The WHO’s global hepatitis strategy aligns with the study’s findings, emphasizing early detection, vaccination, and cost-effective diagnostic tools in endemic regions.

Diagnostic Implications and Recommendations

  • Normal ALT and AST levels were observed in over 90% of patients, but 75% of HBeAg-positive individuals had elevated ALT levels.
  • High viral load (>200,000 IU/mL) was mostly observed in HBeAg-positive patients.

Public Health Significance

Eritrea’s HBV control efforts can benefit from:

  • Expanded vaccination programs targeting high-risk groups.
  • Enhanced access to molecular diagnostic tools.
  • Creation of national treatment guidelines based on serological data.

Call-to-Action

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