Evidence map›Paper›PMID 17522222›Full record

Trial reportJournal of virology2007

Pretreatment sequence diversity differences in the full-length hepatitis C virus open reading frame correlate with early response to therapy.

Maureen J Donlin, Nathan A Cannon, Ermei Yao, Jia Li, Abdus Wahed, Milton W Taylor, Steven H Belle, Adrian M Di Bisceglie, Rajeev Aurora, John E Tavis and 1 more

Open access · greenAbstract readClinical TrialMulticenter Study
In one paragraph

Trial report in Journal of virology, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 48 papers.

0numbers the graph read from it
0cells of the map it votes in
48citing papers in PubMed
6.5field-weighted citation impact, top 3% 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

48 citing papers in PubMed, 113 citations in OpenAlex.

  1. Trial
  2. Trial
  3. Article
  4. Review
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Review
  11. Observational
  12. Review
  13. Article
  14. Article
  15. Article
  16. Review
  17. Hepatitis B and C in African Americans: current status and continued challenges.Clinical gastroenterology and hepatology : the official clinical practice journal of the American Gastroenterological Association · 2014
    Review
  18. Article
  19. New treatments for genotype 1 chronic hepatitis C - focus on simeprevir.Therapeutics and clinical risk management · 2014
    Review
  20. Review
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

11 authors at 3 institutions in 1 country.

Maureen J DonlinDepartment of Molecular Microbiology and Immunology, Saint Louis University School of Medicine, 1402 S. Grand Blvd., Saint Louis, MO 63104, USA.
Nathan A Cannon
Ermei Yao
Jia Li
Abdus Wahed
Milton W Taylor
Steven H Belle
Adrian M Di Bisceglie
Rajeev Aurora
John E Tavis
Virahep-C Study Group
University of Pittsburgh · USSaint Louis University · USIndiana University Bloomington · US

Funding

ZINC GLUCONATE GLYCINE LOZENGES &VITAMIN C EFFECTS ON COMMON COLDM01RR000042 · NCRR · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI RUBENFIRE, MELVYN · 1985 to 2007
$40.8M
Zonisamide in Patients with Neuropathic Pain Associated with Diabetic NeuropathyM01RR000046 · NCRR · UNIV OF NORTH CAROLINA CHAPEL HILL · PI JOY, MELANIE S · 1985 to 2008
$38.5M
ZOLEDRONIC ACID IN PROSTATE CANCERM01RR000645 · NCRR · COLUMBIA UNIV NEW YORK MORNINGSIDE · PI COLTEN, HARVEY R · 1985 to 2006
$27.0M
ZD1839 FOR MALIGNANT ASTROCYTOMA OR GLIOBLASTOMA AND MENINGIOMAM01RR000079 · NCRR · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI KESSLER, DAVID A · 1985 to 2006
$26.0M
Zonulin Antibodies in Intestinal Permeabilitiy in IDDMM01RR016500 · NCRR · UNIVERSITY OF MARYLAND BALTIMORE · PI OSWALD, LYNN M · 2002 to 2009
$20.2M
Study of Viral Resistance to Antiviral Therapy of Chron*U01DK060329 · NIDDK · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI BELLE, STEVEN H. · 2001 to 2005
$8.0M
Response of HCV to Therapy in African AmericansU01DK060345 · NIDDK · SAINT LOUIS UNIVERSITY · PI TAVIS, JOHN E · 2001 to 2005
$1.4M
HCV TREATMENT IN AFRICAN AMERICANS VS NON HISPANIC WHIT*U01DK060352 · NIDDK · UNIVERSITY OF MIAMI SCHOOL OF MEDICINE · PI JEFFERS, LENNOX J · 2001 to 2005
$1.4M
Hepatitis C: host determinants of progression and respo*U01DK060341 · NIDDK · CEDARS-SINAI MEDICAL CENTER · PI YANG, HUIYING · 2001 to 2005
$1.4M
VIRAHEP-C Clinical CenterU01DK060344 · NIDDK · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI LOK, ANNA SF · 2001 to 2005
$1.3M
Baltimore VIRAHEP-C Clinical CenterU01DK060335 · NIDDK · UNIVERSITY OF MARYLAND BALTIMORE · PI HOWELL, CHARLES D · 2001 to 2005
$1.3M
Hepatitis C Antiviral Resistance in African AmericansU01DK060327 · NIDDK · UNIVERSITY OF NORTH CAROLINA CHAPEL HILL · PI FRIED, MICHAEL W · 2001 to 2005
$1.2M
NCRR NIH HHS M01 RR000042NCRR NIH HHS M01 RR000046NCRR NIH HHS M01 RR000079NCRR NIH HHS M01 RR000645NCRR NIH HHS M01 RR016500NIDDK NIH HHS U01 DK060309NIDDK NIH HHS U01 DK060324NIDDK NIH HHS U01 DK060327NIDDK NIH HHS U01 DK060329NIDDK NIH HHS U01 DK060335NIDDK NIH HHS U01 DK060340NIDDK NIH HHS U01 DK060341NIDDK NIH HHS U01 DK060342NIDDK NIH HHS U01 DK060344NIDDK NIH HHS U01 DK060345NIDDK NIH HHS U01 DK060346NIDDK NIH HHS U01 DK060349NIDDK NIH HHS U01 DK060352NIDDK NIH HHS U01 DK60345
6 · The paper itself

Abstract

Pegylated alpha interferon and ribavirin therapy for hepatitis C virus (HCV) genotype 1 infection fails for half of Caucasian American patients (CA) and more often for African Americans (AA). The reasons for these low response rates are unknown. HCV is highly genetically variable, but it is unknown how this variability affects response to therapy. To assess effects of viral diversity on response to therapy, the complete pretreatment genotype 1 HCV open reading frame was sequenced using samples from 94 participants in the Virahep-C study. Sequences from patients with >3.5 log declines in viral RNA levels by day 28 (marked responders) were more variable than those from patients with declines of <1.4 log (poor responders) in NS3 and NS5A for genotype 1a and in core and NS3 for genotype 1b. These correlations remained when all T-cell epitopes were excluded, indicating that these differences were not due to differential immune selection. When the sequences were compared by race of the patients, higher diversity in CA patients was found in E2 and NS2 but only for genotype 1b. Core, NS3, and NS5A can block the action of alpha interferon in vitro; hence, these genetic patterns are consistent with multiple amino acid variations independently impairing the function of HCV proteins that counteract interferon responses in humans, resulting in HCV strains with variable sensitivity to therapy. No evidence was found for novel HCV strains in the AA population, implying that AA patients may be infected with a higher proportion of the same resistant strains that are found in CA patients.

Indexed as

Genetic VariationOpen Reading FramesAdultAmino Acid SequenceAntiviral AgentsBlack or African AmericanDrug CarriersHepacivirusHepatitis CHumansInterferon-alphaInterferon alpha-2MaleMiddle AgedMolecular Sequence DataPolyethylene GlycolsAntiviral AgentsDrug CarriersInterferon-alphaInterferon alpha-2peginterferon alfa-2aPolyethylene GlycolsRecombinant ProteinsRibavirin

Identifiers

PMID17522222
PMCPMC1951276
OpenAlexW2018198271

What OpenQuestion holds

Textmetadata
Read underepoch 390

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.