Evidence map›Paper›PMID 28740342›Full record

ArticleWorld journal of gastroenterology2017

Hepatitis C virus NS5A region mutation in chronic hepatitis C genotype 1 patients who are non-responders to two or more treatments and its relationship with response to a new treatment.

Paloma Muñoz de Rueda, José Manuel Fuentes Rodríguez, Rosa Quiles Pérez, Ana Gila Medina, Ana Belén Martín Álvarez, Jorge Casado Ruíz, Angeles Ruíz Extremera, Javier Salmerón

Abstract read
In one paragraph

Article in World journal of gastroenterology, 2017. 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
–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

4 citing papers in PubMed.

  1. 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

8 authors.

Paloma Muñoz de RuedaPaloma Muñoz de Rueda, José Manuel Fuentes Rodríguez, Rosa Quiles Pérez, Ana Belén Martín Alvarez, Jorge Casado Ruíz, Ángeles Ruíz Extremera, Javier Salmerón, Research Support Unit, San Cecilio University Hospital of Granada, 18014 Granada, Spain.
José Manuel Fuentes RodríguezPaloma Muñoz de Rueda, José Manuel Fuentes Rodríguez, Rosa Quiles Pérez, Ana Belén Martín Alvarez, Jorge Casado Ruíz, Ángeles Ruíz Extremera, Javier Salmerón, Research Support Unit, San Cecilio University Hospital of Granada, 18014 Granada, Spain.
Rosa Quiles PérezPaloma Muñoz de Rueda, José Manuel Fuentes Rodríguez, Rosa Quiles Pérez, Ana Belén Martín Alvarez, Jorge Casado Ruíz, Ángeles Ruíz Extremera, Javier Salmerón, Research Support Unit, San Cecilio University Hospital of Granada, 18014 Granada, Spain.
Ana Gila MedinaPaloma Muñoz de Rueda, José Manuel Fuentes Rodríguez, Rosa Quiles Pérez, Ana Belén Martín Alvarez, Jorge Casado Ruíz, Ángeles Ruíz Extremera, Javier Salmerón, Research Support Unit, San Cecilio University Hospital of Granada, 18014 Granada, Spain.
Ana Belén Martín ÁlvarezPaloma Muñoz de Rueda, José Manuel Fuentes Rodríguez, Rosa Quiles Pérez, Ana Belén Martín Alvarez, Jorge Casado Ruíz, Ángeles Ruíz Extremera, Javier Salmerón, Research Support Unit, San Cecilio University Hospital of Granada, 18014 Granada, Spain.
Jorge Casado RuízPaloma Muñoz de Rueda, José Manuel Fuentes Rodríguez, Rosa Quiles Pérez, Ana Belén Martín Alvarez, Jorge Casado Ruíz, Ángeles Ruíz Extremera, Javier Salmerón, Research Support Unit, San Cecilio University Hospital of Granada, 18014 Granada, Spain.
Angeles Ruíz ExtremeraPaloma Muñoz de Rueda, José Manuel Fuentes Rodríguez, Rosa Quiles Pérez, Ana Belén Martín Alvarez, Jorge Casado Ruíz, Ángeles Ruíz Extremera, Javier Salmerón, Research Support Unit, San Cecilio University Hospital of Granada, 18014 Granada, Spain.
Javier SalmerónPaloma Muñoz de Rueda, José Manuel Fuentes Rodríguez, Rosa Quiles Pérez, Ana Belén Martín Alvarez, Jorge Casado Ruíz, Ángeles Ruíz Extremera, Javier Salmerón, Research Support Unit, San Cecilio University Hospital of Granada, 18014 Granada, Spain.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

aimTo determine the number of mutations in the NS5A region of the hepatitis C virus (HCV) and its relationship to the response to antiviral therapy in patients with chronic hepatitis C genotype 1 who are non-responders to two or more treatments.

methodsSequences within HCV NS5A [PKR binding domain (PKRBD) and the interferon-sensitivity-determining region (ISDR)] were analysed

resultsFor both regions, treatments resulting in SVR were associated with more baseline mutations than were treatments resulting in NVR (SVR

conclusionThe obtained results show that among patients who have shown no response to two or more antiviral treatments, the likelihood of achieving SVR increases with the genetic variability in the ISDR region (≥ 2 mutations or number of substitutions from the HCV-J and HCV-1 prototype), especially when the viral load is greater than 600000 IU/mL.

Indexed as

Antiviral AgentsDrug Resistance, Multiple, ViralDrug Therapy, CombinationFemaleGenotypeHepacivirusHepatitis C, ChronicHumansInterferon-alphaMaleMutationPolyethylene GlycolsProspective StudiesRetrospective StudiesRibavirinRNA-Dependent RNA PolymeraseAntiviral AgentsInterferon-alphaNS-5 protein, hepatitis C virusPolyethylene GlycolsRibavirinRNA-Dependent RNA PolymeraseViral Nonstructural ProteinsChronic hepatitis CInterferon-based therapyInterferon-free therapyNS5A regionNumber of mutationsSustained virological response

Identifiers

PMID28740342
PMCPMC5504369

What OpenQuestion holds

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LicenceCC BY-NC
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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.