PLoS ONE (Jan 2018)

Distribution of HCV genotypes in Belgium from 2008 to 2015.

  • Lobna Bouacida,
  • Vanessa Suin,
  • Veronik Hutse,
  • Michaël Boudewijns,
  • Reinoud Cartuyvels,
  • Laurent Debaisieux,
  • Emmanuel De Laere,
  • Marie Hallin,
  • Nicolas Hougardy,
  • Katrien Lagrou,
  • Els Oris,
  • Elizaveta Padalko,
  • Marijke Reynders,
  • Gatien Roussel,
  • Jean-Marc Senterre,
  • Michel Stalpaert,
  • Dominique Ursi,
  • Carl Vael,
  • Dolores Vaira,
  • Jos Van Acker,
  • Walter Verstrepen,
  • Steven Van Gucht,
  • Benoit Kabamba,
  • Sophie Quoilin,
  • Gaëtan Muyldermans

DOI
https://doi.org/10.1371/journal.pone.0207584
Journal volume & issue
Vol. 13, no. 12
p. e0207584

Abstract

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BackgroundThe knowledge of circulating HCV genotypes and subtypes in a country is crucial to guide antiviral therapy and to understand local epidemiology. Studies investigating circulating HCV genotypes and their trends have been conducted in Belgium. However they are outdated, lack nationwide representativeness or were not conducted in the general population.MethodsIn order to determine the distribution of different circulating HCV genotypes in Belgium, we conducted a multicentre study with all the 19 Belgian laboratories performing reimbursed HCV genotyping assays. Available genotype and subtype data were collected for the period from 2008 till 2015. Furthermore, a limited number of other variables were collected: some demographic characteristics from the patients and the laboratory technique used for the determination of the HCV genotype.ResultsFor the study period, 11,033 unique records collected by the participating laboratories were used for further investigation. HCV genotype 1 was the most prevalent (53.6%) genotype in Belgium, with G1a and G1b representing 19.7% and 31.6%, respectively. Genotype 3 was the next most prevalent (22.0%). Further, genotype 4, 2, and 5 were responsible for respectively 16.1%, 6.2%, and 1.9% of HCV infections. Genotype 6 and 7 comprise the remaining ConclusionThis national monitoring study allowed a clear and objective view of the circulating HCV genotypes in Belgium and will help health authorities in the establishment of cost effectiveness determinations before implementation of new treatment strategies. This baseline characterization of the circulating genotypes is indispensable for a continuous surveillance, especially for the investigation of the possible impact of migration from endemic regions and prior to the increasing use of highly potent direct-acting antiviral (DAA) agents.