Evidence map›Paper›PMID 19749758›Full record

ArticleNature genetics2009

IL28B is associated with response to chronic hepatitis C interferon-alpha and ribavirin therapy.

Vijayaprakash Suppiah, Max Moldovan, Golo Ahlenstiel, Thomas Berg, Martin Weltman, Maria Lorena Abate, Margaret Bassendine, Ulrich Spengler, Gregory J Dore, Elizabeth Powell and 9 more

2 registry-linked trialsAbstract read
PubMed Publisher
In one paragraph

Article in Nature genetics, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 2 registered trials, which are not on this map. Cited by 746 papers, 5 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
746citing papers in PubMed, 5 pooled it
117.0field-weighted citation impact, top 1% 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.

NCT01437969 completednot on this mapstarted 2011, after this paper: background citation

Pharmacogenomics Study on IL28B Genetic Variants in Italian Patients With HCV Chronic Infection naïve to Antiviral Treatment.

TypeobservationalSponsorCasa Sollievo della Sofferenza IRCCSRan2011 to 2022Enrolled500ConditionsLiver DiseaseArmsgenotyping and/or sequencing
NCT01707849 phase3completednot on this mapstarted 2012, after this paper: background citation

An Unicenter, Prospective, Randomized, Pilot Study Comparing the Effect of Everolimus-containing Versus mTOR Inhibitor Free Immunosuppression in the Evolution of Hepatitis C Fibrosis After Liver Transplantation.

TypeinterventionalSponsorHospital Vall d'HebronRan2012 to 2016Enrolled18ConditionsHepatitis C Recurrence After Liver TransplantArmsEVL arm, MMF arm
3 · Its place in the literature

Who cites it

746 citing papers in PubMed, 5 syntheses or guidelines pooled it, 1,814 citations in OpenAlex.

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686 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

19 authors at 7 institutions in 4 countries.

Vijayaprakash SuppiahStorr Liver Unit, University of Sydney, Sydney, Australia.
Max Moldovan
Golo Ahlenstiel
Thomas Berg
Martin Weltman
Maria Lorena Abate
Margaret Bassendine
Ulrich Spengler
Gregory J Dore
Elizabeth Powell
Stephen Riordan
David Sheridan
Antonina Smedile
Vincenzo Fragomeli
Tobias Müller
Melanie Bahlo
Graeme J Stewart
David R Booth
Jacob George
The University of Sydney · AUNepean Hospital · AUUniversity of Bonn · DEThe University of Queensland · AUUniversity of Turin · ITThe University of Melbourne · AUUNSW Sydney · AU

Funding

Medical Research Council G0502028
6 · The paper itself

Abstract

Hepatitis C virus (HCV) infects 3% of the world's population. Treatment of chronic HCV consists of a combination of PEGylated interferon-alpha (PEG-IFN-alpha) and ribavirin (RBV). To identify genetic variants associated with HCV treatment response, we conducted a genome-wide association study of sustained virological response (SVR) to PEG-IFN-alpha/RBV combination therapy in 293 Australian individuals with genotype 1 chronic hepatitis C, with validation in an independent replication cohort consisting of 555 individuals. We report an association to SVR within the gene region encoding interleukin 28B (IL28B, also called IFNlambda3; rs8099917 combined P = 9.25 x 10(-9), OR = 1.98, 95% CI = 1.57-2.52). IL28B contributes to viral resistance and is known to be upregulated by interferons and by RNA virus infection. These data suggest that host genetics may be useful for the prediction of drug response, and they also support the investigation of the role of IL28B in the treatment of HCV and in other diseases treated with IFN-alpha.

Indexed as

AdultAntiviral AgentsAustraliaDrug Therapy, CombinationFemaleGene Expression RegulationGenome-Wide Association StudyGenotypeHepatitis C, ChronicHumansInterferon-alphaInterferon LambdaInterferonsInterleukinsMaleMiddle AgedAntiviral AgentsInterferon-alphaInterferon Lambdainterferon-lambda, humanInterferonsInterleukinsPolyethylene GlycolsRibavirin

Identifiers

PMID19749758
OpenAlexW2086414517

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

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.