Evidence map›Paper›PMID 31364570›Full record

ArticleEpidemiology and infection2019

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

T Semenova, B Nemoz, V Thibault, G Lagathu, G Duverlie, E Brochot, P Trimoulet, C Payan, S Vallet, C Henquell and 10 more

Open access · hybridAbstract readMulticenter Study
In one paragraph

Article in Epidemiology and infection, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.3field-weighted citation impact, top 41% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

4 citing papers in PubMed, 7 citations in OpenAlex.

  1. I Can C Clearly Now, the End Is Near.Digestive diseases and sciences · 2025
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

20 authors at 11 institutions in 1 country.

T SemenovaLaboratoire de Virologie,Institut de Biologie et Pathologie, CHU Grenoble-Alpes,Grenoble,France.
B NemozLaboratoire de Virologie,Institut de Biologie et Pathologie, CHU Grenoble-Alpes,Grenoble,France.ORCID 0000-0002-3843-9380
V ThibaultLaboratoire de Virologie, CHU de Rennes,Rennes,France.
G LagathuLaboratoire de Virologie, CHU de Rennes,Rennes,France.
G DuverlieLaboratoire de Virologie- EA4294 Centre de Biologie Humaine CHU Amiens,Université de Picardie Jules Verne,Amiens,France.
E BrochotLaboratoire de Virologie- EA4294 Centre de Biologie Humaine CHU Amiens,Université de Picardie Jules Verne,Amiens,France.
P TrimouletLaboratoire de Virologie, CHU de Bordeaux,Bordeaux,France.
C PayanDépartement de Bactério-Virologie,Hygiène Hospitalière et Parasito-Mycologie, CHRU La Cavale Blanche,Brest,France.
S ValletDépartement de Bactério-Virologie,Hygiène Hospitalière et Parasito-Mycologie, CHRU La Cavale Blanche,Brest,France.
C HenquellService de Virologie,CHU de Clermont-Ferrand,Clermont-Ferrand,France.
S ChevaliezDépartement de Virologie,Bactériologie-Hygiène, Mycologie-Parasitologie, Unité Transversale de Traitement des Infections,Créteil,France&INSERM U955,Créteil,France.
M Bouvier-AliasDépartement de Virologie,Bactériologie-Hygiène, Mycologie-Parasitologie, Unité Transversale de Traitement des Infections,Créteil,France&INSERM U955,Créteil,France.
S MaylinHôpital Saint Louis,Service de Microbiologie- Pôle B2P,Paris,France.
A-M Roque-AfonsoLaboratoire de Virologie,Hôpitaux Universitaires Paris-Sud, Hôpital Paul Brousse,Villejuif,France.
L IzquierdoLaboratoire de Virologie,Hôpitaux Universitaires Paris-Sud, Hôpital Paul Brousse,Villejuif,France.
F Lunel-FabianiLaboratoire de Virologie,CHU Angers, HIFIH laboratory,UPRES EA 3859,SFR 4208, Angers,France.
P MarcellinService d'Hépatologie,Hôpital Beaujon,Clichy,France.
P MorandLaboratoire de Virologie,Institut de Biologie et Pathologie, CHU Grenoble-Alpes,Grenoble,France.
V LeroyClinique d'Hépato-gastroentérologie,Pôle Digidune,CHU Grenoble-Alpes,Grenoble,France.
S LarratLaboratoire de Virologie,Institut de Biologie et Pathologie, CHU Grenoble-Alpes,Grenoble,France.
Centre Hospitalier Universitaire de Grenoble · FRCentre Hospitalier Régional Universitaire de Brest · FRCentre Hospitalier Universitaire de Rennes · FRHôpital Paul-Brousse · FRInserm · FRUniversité de Picardie Jules Verne · FRCentre Hospitalier Universitaire d'Angers · FRCentre Hospitalier Universitaire de Bordeaux · FRCentre Hospitalier Universitaire de Clermont-Ferrand · FRHôpital Beaujon · FRHôpital Saint-Louis · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

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.

Indexed as

AdultDatabases, FactualFemaleFranceGenotypeHepacivirusHepatitis C, ChronicHumansLiver CirrhosisLogistic ModelsMaleMultivariate AnalysisPrevalenceRetrospective StudiesRNA, ViralSeverity of Illness IndexRNA, ViralViral ProteinsEpidemiologyfibrosisHCV genotypestreatment-naive HCV

Identifiers

PMID31364570
PMCPMC6625182
OpenAlexW2957262117

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.