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  • Poster presentation
  • Open Access

A cohort study in the assessment of liver fibrosis and markers of disease progression in hepatitis B and D coinfection

  • 1Email author,
  • 1, 2,
  • 1, 2,
  • 1, 2,
  • 1, 2 and
  • 1, 2
BMC Infectious Diseases201313 (Suppl 1) :P53

  • Published:


  • Hepatitis
  • Cohort Study
  • Gold Standard
  • Liver Function
  • Promising Result


Given the important role played by hepatitis viruses in the development of liver fibrosis we consider it necessary to evaluate markers of disease progression and instruments for staging of fibrosis in patients coinfected with hepatitis B and D viruses (HBV, HDV).


We performed a cohort study to assess markers of disease progression and staging of liver fibrosis through noninvasive tests at three different time points over the course of HBV and HDV coinfection.


We assessed data from 64 patients (of which 27 were males - 42%) with a median age of 54±14 (range: 23 to 64 years). The median fibrosis was 0.44±0.23 and the median necroinflammatory activity was 0.54±0.24.

The median FIB-4 score was 1.89±3.23 at the second visit versus 1.26±2.07 at the third visit. The median APRI score was 1.18±1.67 at the second visit compared to 1.79±2.53 at the third visit (p=0.05, 95%CI: 0.0389, 0.43681). Regression analysis showed a correlation between FibroTest (considered the gold standard in this study, in the absence of histology data from liver biopsy), FIB-4 (p=0.43) and APRI (p=0.011).


Periodic assessment of patients with viral hepatitis is needed, with close monitoring of fibrosis progression and liver function. Noninvasive markers and scores for liver fibrosis are yet to be validated for patients with HBV and HDV coinfection, but the data from this cohort of patients show promising results, with both APRI and FIB-4 positively correlating with FibroTest.

Authors’ Affiliations

Carol Davila University of Medicine and Pharmacy, Bucharest, Romania
National Institute for Infectious Diseases “Prof. Dr. Matei Balş”, Bucharest, Romania


© Aker et al; licensee BioMed Central Ltd. 2013

This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.