Evidence map›Paper›PMID 24358043›Full record

ArticleHepatitis monthly2013

Amino Acid Polymorphisms Within the Entire HCV NS5A Region in Estonian Chronic HCV 1b Patients With Different Treatment Response.

Tatiana Kuznetsova, Tatjana Tallo, Vadim Brjalin, Irina Reshetnjak, Riina Salupere, Ljudmilla Priimagi, Olga Katargina, Maria Smirnova, Juris Jansons, Valentina Tefanova

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Article in Hepatitis monthly, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
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0citing papers in PubMed
–field-weighted citation impact, top 86% 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

0 citing papers in PubMed, 1 citations in OpenAlex.

No citing paper in PubMed yet.

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

10 authors at 5 institutions in 4 countries.

Tatiana KuznetsovaDepartment of Virology, National Institute for Health Development, Tallinn, Estonia.
Tatjana TalloDepartment of Virology, National Institute for Health Development, Tallinn, Estonia ; Department of Diagnostics and Vaccine, Unit for Molecular Typing, Swedish Institute for Communicable Disease Control, Stockholm, Sweden.
Vadim BrjalinDepartment of Internal Medicine, West-Tallinn Central Hospital, Tallinn, Estonia.
Irina ReshetnjakDepartment of Virology, National Institute for Health Development, Tallinn, Estonia.
Riina SalupereDepartment of Internal Medicine, University of Tartu, Tartu, Estonia.
Ljudmilla PriimagiDepartment of Virology, National Institute for Health Development, Tallinn, Estonia.
Olga KatarginaDepartment of Virology, National Institute for Health Development, Tallinn, Estonia.
Maria SmirnovaDepartment of Hemorrhagic Fevers and Pilot Projects, Federal State Budgetary Institution "Chumakov Institute of Poliomyelitis and Viral Encephalitides" of RAMS, Moscow, Russia.
Juris JansonsProtein Engineering Department, Latvian Biomedical Research and Study Centre, Riga, Latvia.
Valentina TefanovaDepartment of Virology, National Institute for Health Development, Tallinn, Estonia.
National Institute for Health Development · EEChumakov Institute of Poliomyelitis and Viral Encephalitides · RUEast Tallinn Central Hospital · EELatvian Biomedical Research and Study Centre · LVUniversity of Tartu · EE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundA substantial proportion of hepatitis C virus (HCV)-1b infected patients do not response to pegylated interferon-α plus ribavirin (PegIFNα/RBV) combination therapy that was partially associated with mutations in the non-structural 5A (NS5A) protein.

objectivesAnalysis of NS5A polymorphisms in HCV genotype 1b pre-treatment serum samples from Estonian patients and their effect on the treatment response. PATIENTS AND

methodsTwenty-nine complete NS5A sequences obtained from patients with chronic HCV-1b infection who had received combined therapy with PegIFNα-2a/RBV were analyzed and compared with the prototype strain HCV-J. Twelve patients achieved a sustained virological response (SVR), 15 were non-SVR and 2 patients stopped treatment because of side effects.

resultsNo significant difference in total number of amino acid mutations was observed between isolates from SVR and non-SVR patients in any known regions of the NS5A protein. However, specific amino acid substitutions at positions 1989 and 2283 correlated significantly with SVR, mutations at positions 1979, 2107, 2171 and 2382 were associated with non-response to treatment and amino acid substitution at position 2319 was observed in relapsers. At phylogenetic analysis, NS5A nucleotide sequences have been subdivided into four groups characterized by the different treatment response. Twenty-four novel nucleotide polymorphisms and 11 novel amino acid polymorphisms were identified based on the phylogenetic tree topology.

conclusionsSpecific amino acid substitutions correlating with the treatment response were found. Polymorphisms revealed by phylogenetic analysis may define the signature patterns for treatment susceptible and treatment resistant strains prevalent in Estonia.

Indexed as

EstoniaHepatitis CRibavirinTherapy

Identifiers

PMID24358043
PMCPMC3867023
OpenAlexW2169254637

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