Evidence map›Paper›PMID 30517127›Full record

ArticlePloS one2018

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 and 15 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.4field-weighted citation impact, top 35% 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

3 citing papers in PubMed, 9 citations in OpenAlex.

  1. Article
  2. Article
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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

25 authors at 18 institutions in 1 country.

Lobna BouacidaSciensano, Laboratory of medical microbiology, Brussels, Belgium.
Vanessa SuinSciensano, Viral diseases, Brussels, Belgium.
Veronik HutseSciensano, Viral diseases, Brussels, Belgium.
Michaël BoudewijnsAZ Groeninge, Campus Kennedylaan Laboratorium, Kortrijk, Belgium.
Reinoud CartuyvelsJessa Ziekenhuis, Klinisch Laboratorium, Hasselt, Belgium.
Laurent DebaisieuxLHUB-ULB site Anderlecht, CUB-Hôpital Erasme, Brussels, Belgium.
Emmanuel De LaereAZ Delta, Laboratorium, Roeselare, Belgium.
Marie HallinLHUB-ULB, Site Porte De Hal, Brussels, Belgium.ORCID 0000-0003-4544-0635
Nicolas HougardyClin. Sud Luxembourg, Site St-Joseph Labo D'analyses Médicales, Arlon, Belgium.
Katrien LagrouUZ Leuven, Clinical Department of Laboratory Medicine, Leuven, and-KU Leuven, Department of Microbiology and Immunology, Leuven, Belgium.
Els OrisZiekenhuis Oost-Limburg, Labo Klinische Biologie, Genk, Belgium.
Elizaveta PadalkoUZ Ghent, Clinical Biology-Medical Microbiology Laboratory, Ghent, Belgium.
Marijke ReyndersAZ Sint-Jan Brugge-Oostende AV, Laboratory Medicine, Brugge, Belgium.ORCID 0000-0003-2079-1279
Gatien RousselClinique St. Pierre, Laboratoire De Biologie Clinique, Ottignies, Belgium.
Jean-Marc SenterreCh Regional De La Citadelle, Laboratoire, Liège, Belgium.
Michel StalpaertAlgemeen Medisch Labo, Antwerp, Belgium.
Dominique UrsiUniversity Hospital Antwerp, Laboratory of Molecular Diagnostics in Microbiology, Antwerp, Belgium.
Carl VaelAZ KLINA, Clinical Laboratory, Brasschaat, Belgium.
Dolores VairaCHU de Liège, Laboratoire de Référence SIDA-ULg, Liège, Belgium.
Jos Van AckerAZ Sint Lucas, Laboratorium, Gent, Belgium.
Walter VerstrepenZNA, Klinisch Laboratorium Campus Middelheim, Antwerp, Belgium.
Steven Van GuchtSciensano, Viral diseases, Brussels, Belgium.ORCID 0000-0002-8150-9372
Benoit KabambaCliniques Universitaires Saint-Luc, Labo Biologie Clinique Ria, Brussels, Belgium.
Sophie QuoilinSciensano, Epidemiology of infectious diseases, Brussels, Belgium.
Gaëtan MuyldermansSciensano, Epidemiology of infectious diseases, Brussels, Belgium.ORCID 0000-0002-2188-8307
Sciensano (Belgium) · BEAntwerp University Hospital · BEAZ Delta · BEAZ Groeninge · BEAZ Klina · BEAZ Sint-Jan · BEAZ Sint-Lucas · BECentre hospitalier régional de la Citadelle · BECentre Hospitalier Universitaire de Liège · BEClinique Saint Pierre · BECliniques du Sud Luxembourg · BECliniques Universitaires Saint-Luc · BEErasmus Hospital · BEGhent University Hospital · BEJessa Hospital · BEUniversitair Ziekenhuis Leuven · BEZiekenhuis Oost-Limburg · BEZNA Middelheim Hospital · BE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

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 <1%. Throughout the years, a stable distribution was observed for most genotypes. Only for genotype 5, a decrease as a function of the year of analysis was observed, with respectively 3.6% for 2008, 2.3% for 2009 and 1.6% for the remaining years. The overall M:F ratio was 1.59 and was mainly driven by the high M:F ratio of 3.03 for patients infected with genotype 3. Patients infected with genotype 3 are also younger (mean age 41.7 years) than patients infected with other genotypes (mean age above 50 years for all genotypes). The patients for whom a genotyping assay was performed in 2008 were younger than those from 2015. Geographical distribution demonstrates that an important number of genotyped HCV patients live outside the Belgian metropolitan cities.

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.

Indexed as

AdultAgedBelgiumFemaleGenotypeHepacivirusHepatitis CHepatitis C, ChronicHumansMaleMiddle AgedPrevalence

Identifiers

PMID30517127
PMCPMC6281185
OpenAlexW2903446768

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.