Evidence map›Paper›PMID 26684004›Full record

ArticleVirology journal2015

Kinetic response of wild and mutant core codon 70 strains of HCV genotype 1b to pegylated interferon-α and ribavirin therapy.

Zhongjie Hu, Ying Liu, Lixia Qiu, Zuopeng Fan, Wei Nie, Shan Liang, Ronghua Jin

Open access · goldAbstract readClinical Study
In one paragraph

Article in Virology journal, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.5field-weighted citation impact, top 34% 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

1 citing paper in PubMed, 4 citations in OpenAlex.

  1. Article
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

7 authors at 2 institutions in 1 country.

Zhongjie HuDepartment of Hepatitis C & Toxic liver diseases, Beijing Youan Hospital, Capital Medical University, Beijing, the People's Republic of China. yfcyt@139.com.
Ying LiuManagement center of medical record, Beijing Youan Hospital, Capital Medical University, Beijing, the People's Republic of China. lyhzj2006@126.com.
Lixia QiuDepartment of Hepatitis C & Toxic liver diseases, Beijing Youan Hospital, Capital Medical University, Beijing, the People's Republic of China. jslygxc@sina.com.
Zuopeng FanDepartment of Hepatitis C & Toxic liver diseases, Beijing Youan Hospital, Capital Medical University, Beijing, the People's Republic of China. yunji8131@sina.com.
Wei NieDepartment of Hepatitis C & Toxic liver diseases, Beijing Youan Hospital, Capital Medical University, Beijing, the People's Republic of China. shuqing4000@sina.com.
Shan LiangDepartment of Hepatitis C & Toxic liver diseases, Beijing Youan Hospital, Capital Medical University, Beijing, the People's Republic of China. cat216@163.com.
Ronghua JinBeijing Youan Hospital, Capital Medical University, No. 8 Xitoutiao, Youanmenwai, Fengtai District, Beijing, 100069, the People's Republic of China. jinronghua321@sina.com.
Beijing YouAn Hospital · CNCapital Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAmino acid (aa) 70 substitution (R70Q/H) in the core protein of hepatitis C virus (HCV) genotype 1b has been shown to be one of the key factors in determining resistance for pegylated interferon-α plus ribavirin combination therapy (PEG-IFNα/RBV). But the exact mechanisms remain unclear. The aim of this study was to investigate the dynamic response of wild and mutant core codon 70 strains to PEG-IFNα/RBV treatment.

methodsOne hundred twelve Chinese patients with chronic HCV 1b infection were enrolled and received a standard protocol of 48 weeks of PEG-IFNα/RBV therapy and 24 consecutive weeks of follow-up. Serial blood samples were obtained at pretreatment baseline, and again at weeks 2, 4, 8, 12, and 24 during therapy for the quantification of 70R and 70Q/H strains. Dynamic characteristics and association with early virological response (EVR), sustained virological response (SVR) and IL28B genotypes were analyzed.

resultsOf the 112 patients enrolled in this study, 93.8% (105/112) were infected with mixture of 70R and 70Q/H strains before treatment. The 70Q/H strain was dominant in 20.5% of patients. 42.9% of patients with dominant 70Q/H exhibited EVR versus 88.6% of patients with dominant 70R (P < 0.001). Furthermore, 35.0% of patients with dominant 70Q/H exhibited SVR versus 77.4% with dominant 70R (P < 0.001). However, regardless of the dominant strain, virological response types or the IL28B SNP genotypes, 70Q/H strains always exhibited the same response to treatment as the 70R strains and the percentage of HCV harboring the 70Q/H substitution did not change significantly during treatment.

conclusionsAlthough the ratio of 70Q/H to 70R is related to the virological response, 70Q/H strains always exhibited the same response as the 70R strains during PEG-IFNα/RBV treatment. Substitution of R70Q/H alone is not enough to lead to resistance to therapy. Positive selection for 70Q/H induced by IFNα was not observed.

Indexed as

GenotypeAdultAgedAmino Acid SubstitutionAntiviral AgentsBloodChinaDrug Resistance, ViralFemaleHepacivirusHepatitis C, ChronicHumansInterferon-alphaMaleMiddle AgedRibavirinAntiviral AgentsInterferon-alphanucleocapsid protein, Hepatitis C virusRibavirinViral Core Proteins

Identifiers

PMID26684004
PMCPMC4683707
OpenAlexW2210972066

What OpenQuestion holds

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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.