Evidence map›Paper›PMID 24628791›Full record

ArticleVirology journal2014

Genetic heterogeneity of hepatitis C virus cell entry receptors seems to have no influence on selection of virus variants.

Maren Lipskoch, Manfred Wiese, Joerg Timm, Michael Roggendorf, Sergei Viazov

Open access · goldAbstract read
In one paragraph

Article in Virology journal, 2014. 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
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact, top 88% 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

5 authors at 3 institutions in 1 country.

Maren Lipskoch
Manfred Wiese
Joerg Timm
Michael Roggendorf
Sergei ViazovInstitute of Virology, Essen University Hospital, University of Duisburg-Essen, Essen, Germany. sergei.viazov@uni-due.de.
University of Duisburg-Essen · DEEssen University Hospital · DEUniversity Hospital Leipzig · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundNo information is available on the possible influence of the genetic heterogeneity of major hepatitis C virus (HCV) cell receptors on selection of virus variants.

findingsAnti-D globulin preparations contaminated with the HCV strain AD78 caused hepatitis C infection in more than 3000 women in East Germany in 1978. Analysis of the core to NS2 gene sequences of this strain in several globulin batches revealed the presence of three closely related but distinct virus variants of the same strain. Apparently even distribution of these three virus variants was observed in 91 patients infected with the AD78 strain. None of these patients was infected with more than one virus variant, suggesting a selection mechanism of a particular virus variant in each patient. To verify the hypothesis that heterogeneity of HCV cell receptors might influence the virus variant selection, single-nucleotide polymorphisms (SNPs) in low-density lipoprotein receptor (LDLR), occludin (OCLN), and scavenger receptor B1 (SCARB1) genes in AD patients were analyzed. No evident correlation between receptor polymorphisms and presence of a particular virus variant was noted.

conclusionSNPs of HCV cell entry receptors have no influence on virus selection in patients infected with an inoculum containing different virus variants.

Indexed as

Genetic HeterogeneityVirus InternalizationFemaleGermany, EastHepacivirusHumansOccludinPolymorphism, Single NucleotideReceptors, LDLReceptors, VirusScavenger Receptors, Class BSelection, GeneticLDLR protein, humanOccludinOCLN protein, humanReceptors, LDLReceptors, VirusSCARB1 protein, humanScavenger Receptors, Class B

Identifiers

PMID24628791
PMCPMC4007597
OpenAlexW2118784028

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.