Evidence map›Paper›PMID 30387174›Full record

ArticleHepatology (Baltimore, Md.)2019

Highly Diverse Hepatitis C Strains Detected in Sub-Saharan Africa Have Unknown Susceptibility to Direct-Acting Antiviral Treatments.

Chris Davis, George S Mgomella, Ana da Silva Filipe, Eric H Frost, Genevieve Giroux, Joseph Hughes, Catherine Hogan, Pontiano Kaleebu, Gershim Asiki, John McLauchlan and 13 more

Abstract readMulticenter Study
In one paragraph

Article in Hepatology (Baltimore, Md.), 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed, 1 pooled it
–field-weighted citation impact
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

24 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Article
  3. Review
  4. Article
  5. Article
  6. Malignancy and viral infections in Sub-Saharan Africa: A review.Frontiers in virology (Lausanne, Switzerland) · 2023
    Article
  7. Article
  8. Article
  9. DAA Treatment Failure in a HIV/HBV/HCV Co-Infected Patient Carrying a Chimeric HCV Genotype 4/1b.International journal of environmental research and public health · 2022
    Article
  10. Article
  11. Article
  12. Article
  13. Review
  14. Article
  15. Article
  16. Article
  17. Article
  18. Viral hepatitis and pregnancy.Nature reviews. Gastroenterology & hepatology · 2021
    Review
  19. Article
  20. Evidence of tenofovir resistance in chronic hepatitis B virus (HBV) infection: An observational case series of South African adults.Journal of clinical virology : the official publication of the Pan American Society for Clinical Virology · 2020
    Observational
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

23 authors.

Chris DavisMedical Research Council - University of Glasgow Centre for Virus Research, Glasgow, United Kingdom.
George S MgomellaDepartment of Medicine - University of Cambridge, Cambridge, Cambridgeshire, United Kingdom.ORCID 0000-0002-9525-7612
Ana da Silva FilipeMedical Research Council - University of Glasgow Centre for Virus Research, Glasgow, United Kingdom.
Eric H FrostUniversity of Sherbrooke, Sherbrooke, Quebec, Canada.
Genevieve GirouxUniversity of Sherbrooke, Sherbrooke, Quebec, Canada.
Joseph HughesMedical Research Council - University of Glasgow Centre for Virus Research, Glasgow, United Kingdom.
Catherine HoganUniversity of Sherbrooke, Sherbrooke, Quebec, Canada.
Pontiano KaleebuMedical Research Council/Uganda Virus Research Institute & London School of Hygiene and Tropical Medicine Uganda Research Unit, Entebbe, Uganda.
Gershim AsikiUganda Virus Research Institute, Entebbe, Uganda.
John McLauchlanMedical Research Council - University of Glasgow Centre for Virus Research, Glasgow, United Kingdom.
Marc NiebelMedical Research Council - University of Glasgow Centre for Virus Research, Glasgow, United Kingdom.
Ponsiano OcamaDepartment of Medicine, Makerere University College of Health Sciences, Kampala, Uganda.
Cristina PomilaDepartment of Medicine - University of Cambridge, Cambridge, Cambridgeshire, United Kingdom.
Oliver G PybusDepartment of Zoology, University of Oxford, Oxford, United Kingdom.
Jacques PépinUniversity of Sherbrooke, Sherbrooke, Quebec, Canada.
Peter SimmondsPeter Medawar Building for Pathogen Research, University of Oxford, United Kingdom.
Joshua B SingerMedical Research Council - University of Glasgow Centre for Virus Research, Glasgow, United Kingdom.
Vattipally B SreenuMedical Research Council - University of Glasgow Centre for Virus Research, Glasgow, United Kingdom.
Clara WekesaUganda Virus Research Institute, Entebbe, Uganda.
Elizabeth H YoungDepartment of Medicine - University of Cambridge, Cambridge, Cambridgeshire, United Kingdom.
Donald G MurphyNational Institute of Public Health of Quebec, Laboratory of Public Health of Quebec, Sainte-Anne-de-Bellevue, Quebec, Canada.
Manj SandhuDepartment of Medicine - University of Cambridge, Cambridge, Cambridgeshire, United Kingdom.
Emma C ThomsonMedical Research Council - University of Glasgow Centre for Virus Research, Glasgow, United Kingdom.ORCID 0000-0003-1482-0889

Funding

Medical Research Council G0801566Medical Research Council G0901213Medical Research Council G0901213-92157Medical Research Council MC PC 16045Medical Research Council MC_PC_16045Medical Research Council MC_UU_00027/1Medical Research Council MC_UU_12014/1Medical Research Council MC_UU_12014/12Medical Research Council MR/K013491/1Wellcome TrustWellcome Trust 102789/Z/13/A
6 · The paper itself

Abstract

The global plan to eradicate hepatitis C virus (HCV) led by the World Health Organization outlines the use of highly effective direct-acting antiviral drugs (DAAs) to achieve elimination by 2030. Identifying individuals with active disease and investigation of the breadth of diversity of the virus in sub-Saharan Africa (SSA) is essential as genotypes in this region (where very few clinical trials have been carried out) are distinct from those found in other parts of the world. We undertook a population-based, nested case-control study in Uganda and obtained additional samples from the Democratic Republic of Congo (DRC) to estimate the prevalence of HCV, assess strategies for disease detection using serological and molecular techniques, and characterize genetic diversity of the virus. Using next-generation and Sanger sequencing, we aimed to identify strains circulating in East and Central Africa. A total of 7,751 Ugandan patients were initially screened for HCV, and 20 PCR-positive samples were obtained for sequencing. Serological assays were found to vary significantly in specificity for HCV. HCV strains detected in Uganda included genotype (g) 4k, g4p, g4q, and g4s and a newly identified unassigned g7 HCV strain. Two additional unassigned g7 strains were identified in patients originating from DRC (one partial and one full open reading frame sequence). These g4 and g7 strains contain nonstructural (ns) protein 3 and 5A polymorphisms associated with resistance to DAAs in other genotypes. Clinical studies are therefore indicated to investigate treatment response in infected patients. Conclusion: Although HCV prevalence and genotypes have been well characterized in patients in well-resourced countries, clinical trials are urgently required in SSA, where highly diverse g4 and g7 strains circulate.

Indexed as

AgedAged, 80 and overCross-Sectional StudiesDrug Resistance, ViralEpitopesFemaleGenome, ViralHepacivirusHepatitis CHumansMaleMiddle AgedPhylogenySeroepidemiologic StudiesUgandaViral LoadEpitopes

Identifiers

PMID30387174
PMCPMC6492010

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.