Hepatitis C subtype distribution in chronically infected patients with mild liver fibrosis in France: the GEMHEP

T Semenova1, B Nemoz1, V Thibault2

  • 1Laboratoire de Virologie,Institut de Biologie et Pathologie, CHU Grenoble-Alpes,Grenoble,France.

Insights

Direct-acting antiviral (DAA) treatment for Hepatitis C virus (HCV) is effective, but access is limited. This study found genotypes 1b and 1a are most common in French patients with mild fibrosis, but more data is needed on genotype 4 efficacy.

Area of Science:

  • Hepatology
  • Virology
  • Epidemiology

Background:

  • Direct-acting antiviral (DAA) combinations offer high cure rates for Hepatitis C virus (HCV) infection.
  • Treatment access is often restricted to patients with advanced fibrosis (F3-F4) due to high costs.
  • Understanding the epidemiology of HCV in patients with milder fibrosis (F0-F2) is crucial for assessing treatment eligibility.

Purpose of the Study:

  • To investigate the epidemiological characteristics and genotype distribution of HCV in treatment-naive patients with METAVIR fibrosis stages F0-F2 in France.
  • To identify patient profiles eligible for unrestricted DAA treatment based on genotype prevalence.
  • To inform public health strategies and clinical management of HCV in France.

Main Methods:

  • Retrospective data collection from nine French university hospitals between 2015 and 2016.
  • Inclusion of 584 treatment-naive HCV-positive patients with METAVIR fibrosis stages F0-F2.
  • Hepatitis C virus (HCV) genotyping to determine the distribution of different viral types.

Main Results:

  • Genotype 1b (27.2%) and 1a (25.7%) were the most prevalent genotypes in patients with mild fibrosis.
  • Genotype 4 (13.7%) was also frequently observed, with subtype 4a being predominant (27.5% of genotype 4).
  • Genotypes 1b and 1a are readily treatable with current DAAs, but efficacy data for genotype 4 subtypes is limited.

Conclusions:

  • Hepatitis C virus (HCV) epidemiology in France shows a high prevalence of genotypes 1b and 1a in patients with mild fibrosis.
  • The increasing prevalence of 'non-a non-d' genotype 4, often linked to African populations, requires further investigation regarding DAA treatment efficacy.
  • Additional clinical data on DAA effectiveness against genotype 4 is necessary to guide treatment decisions and improve patient care.

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