Assessment of Liver Fibrosis in HBsAg-Negative and Anti HBc Positive Patients
- 1 Department of Hepato-Gastroenterology, Yalgado Ouedraogo University Hospital (CHU-YO), Ouagadougou, Burkina Faso
- 2 Department of Hepato-Gastroenterology, Yalgado Ouedraogo University Hospital (CHU-YO), Ouagadougou, Burkina Faso
- 3 Department of Hepato-Gastroenterology, Yalgado Ouedraogo University Hospital (CHU-YO), Ouagadougou, Burkina Faso
- 4 Department of Medicine, University Joseph KI-ZERBO, Ouagadougou, Burkina Faso
- 5 Department of Hepato-Gastroenterology, Yalgado Ouedraogo University Hospital (CHU-YO), Ouagadougou, Burkina Faso
- 6 Department of Hepato-Gastroenterology, Yalgado Ouedraogo University Hospital (CHU-YO), Ouagadougou, Burkina Faso
- 7 Department of Hepato-Gastroenterology, Yalgado Ouedraogo University Hospital (CHU-YO), Ouagadougou, Burkina Faso
Abstract
Background: Surface antigen (HBsAg) is the mean marker of hepatitis B virus infection. During the course of the infection, some patients lose the HBsAg and only the presence of anti-HBc antibody indicates previous contact with the virus. Among these patients, some have detectable viral load (occult infection) but most without viral replication. There is no guideline regarding these patients. The aim of this study was to assess hepatic fibrosis in patients with only the hepatitis B virus contact marker “total anti-HBc”. Patients and methods: it was a descriptive and analytical cross-sectional study, conducted in three private hospitals from January to August 2022. Were included HBsAg-negative and HBc-positive patients, consulting in Gastroenterology departments. Noninvasive methods (APRI, FIB-4 and FIBROSCAN) were used to evaluate liver stiffness because of their easy accessibility and low-cost. The hepatic fibrosis was considered significant when the score determined by APRI, FIB-4 and FIBROSCAN® tests was respectively greater than 1.5; 2.67 and 8 kPa corresponding to fibrosis level 2 (F2). Results: A total of 63 HBsAg-negative/total HBcAg-positive patients were included. The mean age was 49.9 ± 13.4 years. The male/female sex ratio was 1.78. Of the 63 patients, 19 had significant liver fibrosis (30.1%) among which 9 patients had HCC. The FIB-4 score outperformed the APRI score in assessing liver fibrosis, with a sensitivity of 84.2%, a specificity of 100% and a negative predictive value of 93.6%. In univariate analysis, there was a significant association between the occurrence of significant liver fibrosis and age over 40 years, dyslipidaemia, obesity, alcohol consumption, smoking, herbal medicine, negative anti-HBs immunological status and detectable viral load. Conclusion: Our study revealed a high prevalence of significant to severe hepatic fibrosis in anti-HBc positive patients. In most of the cases, the fibrosis was severe. Progression to HCC has also been possible. There is no consensus on the follow-up strategy for those patients. However, screening for hepatic fibrosis using noninvasive methods should be recommended for patients aged over 40 years, alcohol or herbal medicine users, patients with metabolic syndrome or occult hepatitis B. In HBsAg-negative/anti-HBc-positive patients, liver stiffness should be evaluated and if it is greater than F2, HCC screening should be started.
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