Evaluation of Chronic Hepatitis B Infection in Patients with Seronegative HbsAg

E Gholami Parizad1, A Khosravi, E Gholami Parizad

  • 1Dept. of Microbiology, Faculty of Medicine, Ilam University of Medical Sciences, Ilam, Iran.

Insights

Hepatitis B virus (HBV) DNA was detected in biological fluids of chronic hepatitis patients and controls. PCR and Real Time PCR are more reliable for detecting HBV carriers than ELISA alone.

Area of Science:

  • Hepatology
  • Virology
  • Molecular Diagnostics

Background:

  • Hepatitis B virus (HBV) infection is a global health concern, with an estimated 370 million chronic carriers worldwide.
  • Approximately 3% of the Iranian population are chronic HBV carriers.
  • Routine diagnostic tests may underestimate the prevalence of chronic HBV infection.

Purpose of the Study:

  • To evaluate the presence of HBV DNA in biological fluids of chronic hepatitis patients compared to a control group.
  • To compare the diagnostic efficacy of ELISA, PCR, and Real Time PCR for HBV detection.

Main Methods:

  • A case-control study involving 70 chronic hepatitis patients and a control group.
  • Detection of HBV DNA using Enzyme-Linked Immunosorbent Assay (ELISA), Polymerase Chain Reaction (PCR), and Real Time PCR.

Main Results:

  • 100% of the case group tested positive for HBsAg, compared to 2.8% in the control group.
  • PCR and Real Time PCR identified approximately 7% of the control group as chronic HBV carriers, a higher detection rate than ELISA.
  • Significant viral DNA loads were detected in both serum and ear cerumen samples, highlighting the importance of diverse biological fluids and methods for detection.

Conclusions:

  • The prevalence of chronic HBV carriers is likely higher than currently diagnosed by routine methods.
  • ELISA is insufficient as a standalone screening test for chronic HBV carriers.
  • PCR and Real Time PCR offer superior reliability for detecting and screening chronic HBV carriers.
Abstract

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