France is a low-endemicity country for hepatitis B virus (HBV) infection. In 2016, the prevalence of chronic HBV infection in the general population was estimated at 0.3%, corresponding to more than 135,000 HBsAg-positive individuals, of whom 82% were unaware of their infection. Data on hepatitis D virus (HDV) infection remain limited; however, available studies suggest a prevalence of 6% to 10% among HBsAg-positive individuals. Despite current guideline recommendations, up to 35% of newly diagnosed HBsAg-positive patients between 2018 and 2022 were not screened for HDV infection. The World Health Organization (WHO) targets for 2030 include a 90% reduction in the incidence of chronic viral hepatitis, a 65% reduction in hepatitis-related mortality, and treatment coverage for 80% of eligible diagnosed individuals. Achieving these goals will require strengthening HBV and HDV screening strategies and improving linkage to care and retention throughout the care cascade. Objectives: The primary objective is to assess the severity of liver disease, including significant fibrosis (≥F2) and cirrhosis (F4), among adults newly diagnosed with chronic HBV infection (with or without HDV infection) at Expert/Reference Hepatology Centers and Hepatology or Infectious Diseases Departments. The secondary objectives are to: 1. Describe demographic and virological characteristics of HBsAg-positive patients; 2. Determine the proportion of patients eligible for HBV treatment and evaluate treatment response at 6 and 12 months; 3. Assess the utility of novel virological markers for classifying patients according to phases of chronic HBV infection; 4. Evaluate HBsAg thresholds, in combination with other markers, for distinguishing HBeAg-negative chronic infection from HBeAg-negative chronic hepatitis; 5. Compare clinical and virological characteristics of HBV-monoinfected and HBV/HDV-coinfected patients; 6. Identify molecular signatures associated with liver disease severity; 7. Compare findings with those of a national cohort conducted 15 years earlier; 8. Collect biological samples for future analyses; 9. Assess the clinical utility of a highly sensitive HBcrAg assay. Method: This is a multicenter, observational study including all adults aged ≥18 years with chronic HBV infection, whether managed as outpatients or inpatients, who are newly referred to Expert/Reference Hepatology Centers or to Hepatology or Infectious Diseases Departments. Conclusions: This study will generate updated national data on liver disease severity, treatment eligibility, and virological characteristics among adults newly diagnosed with chronic HBV infection in France.
Study Type
OBSERVATIONAL
Enrollment
1,360
Stéphane Chevaliez
Créteil, France
Proportion of patients with significant fibrosis (METAVIR score ≥F2), including cirrhosis (METAVIR score F4)
Liver disease severity assessed by non-invasive methods (liver stiffness measurement, direct or indirect serum biomarkers, composite scores such as FIB-4) and/or liver biopsy. Significant fibrosis is defined as METAVIR score F2 or higher
Time frame: Baseline (at inclusion)
Demographic characteristics of newly identified chronic HBsAg carriers
age, sex, country of birth
Time frame: Baseline (at inclusion)
Virological characteristics of newly identified chronic HBsAg carriers
HBe status, HBV DNA level, genotype, HBsAg level, HBcrAg level, HBV RNA level, HIV or HCV coinfections
Time frame: Baseline (at inclusion)
Antiviral treatment eligibility and response
ALT and AST levels, HBV DNA level, HBsAg level, HBe status and severity of liver disease
Time frame: Baseline (at inclusion), 6 months and 12 months
Performance of novel virological markers (HBcrAg level and HBV RNA level) in identifying patients at risk of disease progression
ALT and AST levels, HBV DNA level, HBsAg level, HBe status, severity of liver disease (METAVIR score), HBcrAg level and HBV RNA level
Time frame: Baseline (at inclusion)
Diagnostic performance of HBsAg thresholds, in combination with other virological markers for distinguishing HBeAg-negative chronic HBV infection from HBeAg-negative chronic hepatitis B
HBsAg levels, HBe status and HBV DNA levels
Time frame: Baseline (at inclusion)
Characteristics of HDV infection
ALT and AST levels, HBV DNA level, HBsAg and HBcrAg levels, HBe status, HBV genotype, severity of liver disease and proportion of patients treated with bulevirtide with or without pegylated interferon
Time frame: Baseline (at inclusion)
Genome sequence analysis and identification of HBV motifs associated with the severity of liver disease in HBV/HDV-coinfected patients
Whole genome sequence analysis using next-generation sequencing technology
Time frame: Baseline (at inclusion)
Comparison with previous French cohort data (2008-2012)
Evolution of clinical, biological and demographical characteristics of participants enrolled between 2008 and 2012
Time frame: Baseline (at inclusion)
Biobank collection
Collection and storage of whole blood samples
Time frame: Baseline (at inclusion)
Clinical performance of ultra-sensitive HBcrAg assay (iTACT-HBcrAg)
sensitivity, specificity, positive and negative predictive values
Time frame: Baseline (at inclusion)
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