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


Journal

Epidemiology and infection
ISSN: 1469-4409
Titre abrégé: Epidemiol Infect
Pays: England
ID NLM: 8703737

Informations de publication

Date de publication:
01 2019
Historique:
entrez: 1 8 2019
pubmed: 1 8 2019
medline: 3 4 2020
Statut: ppublish

Résumé

Treatment options for Hepatitis C infection have greatly improved with direct-acting antiviral (DAA) combinations achieving high cure rates. Nevertheless, the cost of this treatment is still high and access to treatment in many countries has been preferentially reserved for patients with more severe fibrosis (F3 and F4). In this French nationwide study, we investigated the epidemiological characteristics and genotype distribution of hepatitis C virus (HCV) in treatment-naive patients with METAVIR fibrosis stages between F0 and F2 in order to identify patient profiles that became eligible for unrestricted treatment in a second period. Between 2015 and 2016 we collected data from nine French university hospitals on a total of 584 HCV positive patients with absent, mild or moderate liver fibrosis. The most represented genotypes were genotype 1b (159/584; 27.2%), followed by genotype 1a (150/584; 25.7%); genotype 3 (87/584: 14.9%); genotype 4 (80/584; 13.7%). Among genotype 4: 4a was predominantly encountered with 22 patients (27.5% of genotype 4). Genotypes 1b and 1a are currently the most frequent virus types present in treatment-naive patients with mild fibrosis in France. They can be readily cured using the available DAA. Nevertheless, non-a/non-d genotype 4 is also frequent in this population and clinical data on the efficacy of DAA on these subtypes is missing. The GEMHEP is the French group for study and evaluation of viral hepatitis on a national scale. Data collection on epidemiological and molecular aspects of viral hepatitis is performed on a regular basis in all main French teaching hospitals and serves as a basis for surveillance of these infections. Analysis and trends are regularly published on behalf of the GEMHEP group. Data collection was performed retrospectively over the 2015-2016 period, covering nine main university hospitals in France. A total of 584 hepatitis C positive patients were included in this study. Genotyping of the circulating viruses showed a high prevalence of genotypes 1b and 1a in our population. The epidemiology of hepatitis C is slowly changing in France, particularly as a consequence of the rise of 'non-a non-d' genotype 4 viruses mainly originating from African populations. More data concerning treatment efficacy of these genotypes is needed in order to guide clinical care.

Identifiants

pubmed: 31364570
pii: S0950268819001225
doi: 10.1017/S0950268819001225
pmc: PMC6625182
doi:

Substances chimiques

RNA, Viral 0
Viral Proteins 0

Types de publication

Journal Article Multicenter Study Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

e234

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Auteurs

T Semenova (T)

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

B Nemoz (B)

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

V Thibault (V)

Laboratoire de Virologie, CHU de Rennes,Rennes,France.

G Lagathu (G)

Laboratoire de Virologie, CHU de Rennes,Rennes,France.

G Duverlie (G)

Laboratoire de Virologie- EA4294 Centre de Biologie Humaine CHU Amiens,Université de Picardie Jules Verne,Amiens,France.

E Brochot (E)

Laboratoire de Virologie- EA4294 Centre de Biologie Humaine CHU Amiens,Université de Picardie Jules Verne,Amiens,France.

P Trimoulet (P)

Laboratoire de Virologie, CHU de Bordeaux,Bordeaux,France.

C Payan (C)

Département de Bactério-Virologie,Hygiène Hospitalière et Parasito-Mycologie, CHRU La Cavale Blanche,Brest,France.

S Vallet (S)

Département de Bactério-Virologie,Hygiène Hospitalière et Parasito-Mycologie, CHRU La Cavale Blanche,Brest,France.

C Henquell (C)

Service de Virologie,CHU de Clermont-Ferrand,Clermont-Ferrand,France.

S Chevaliez (S)

Département de Virologie,Bactériologie-Hygiène, Mycologie-Parasitologie, Unité Transversale de Traitement des Infections,Créteil,France&INSERM U955,Créteil,France.

M Bouvier-Alias (M)

Département de Virologie,Bactériologie-Hygiène, Mycologie-Parasitologie, Unité Transversale de Traitement des Infections,Créteil,France&INSERM U955,Créteil,France.

S Maylin (S)

Hôpital Saint Louis,Service de Microbiologie- Pôle B2P,Paris,France.

A-M Roque-Afonso (AM)

Laboratoire de Virologie,Hôpitaux Universitaires Paris-Sud, Hôpital Paul Brousse,Villejuif,France.

L Izquierdo (L)

Laboratoire de Virologie,Hôpitaux Universitaires Paris-Sud, Hôpital Paul Brousse,Villejuif,France.

F Lunel-Fabiani (F)

Laboratoire de Virologie,CHU Angers, HIFIH laboratory,UPRES EA 3859,SFR 4208, Angers,France.

P Marcellin (P)

Service d'Hépatologie,Hôpital Beaujon,Clichy,France.

P Morand (P)

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

V Leroy (V)

Clinique d'Hépato-gastroentérologie,Pôle Digidune,CHU Grenoble-Alpes,Grenoble,France.

S Larrat (S)

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

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