Evidence map›Paper›PMID 24488144›Full record

ArticleClinical pharmacology and therapeutics2014

Drug resistance of a viral population and its individual intrahost variants during the first 48 hours of therapy.

D S Campo, P Skums, Z Dimitrova, G Vaughan, J C Forbi, C G Teo, Y Khudyakov, D T-Y Lau

Open access · greenAbstract read
In one paragraph

Article in Clinical pharmacology and therapeutics, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.6field-weighted citation impact, top 17% 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

6 citing papers in PubMed, 22 citations in OpenAlex.

  1. Reconstruction of Viral Variants via Monte Carlo Clustering.Journal of computational biology : a journal of computational molecular cell biology · 2023
    Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. 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

8 authors at 2 institutions in 1 country.

D S CampoDivision of Viral Hepatitis, Centers for Disease Control and Prevention, Atlanta, Georgia, USA.
P SkumsDivision of Viral Hepatitis, Centers for Disease Control and Prevention, Atlanta, Georgia, USA.
Z DimitrovaDivision of Viral Hepatitis, Centers for Disease Control and Prevention, Atlanta, Georgia, USA.
G VaughanDivision of Viral Hepatitis, Centers for Disease Control and Prevention, Atlanta, Georgia, USA.
J C ForbiDivision of Viral Hepatitis, Centers for Disease Control and Prevention, Atlanta, Georgia, USA.
C G TeoDivision of Viral Hepatitis, Centers for Disease Control and Prevention, Atlanta, Georgia, USA.
Y KhudyakovDivision of Viral Hepatitis, Centers for Disease Control and Prevention, Atlanta, Georgia, USA.
D T-Y LauLiver Center, Division of Gastroenterology, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, Massachusetts, USA.
Centers for Disease Control and Prevention · USBeth Israel Deaconess Medical Center · US

Funding

ZINC STATUS AND T CELL DISORDER IN MILD HUMAN ZINC DEFICIENCYM01RR001032 · NCRR · BETH ISRAEL DEACONESS MEDICAL CENTER · PI MANTZOROS, CHRISTOS S · 1985 to 2008
$32.3M
Racial Differences in IFN Transcriptional ResponseR01DK068598 · NIDDK · UNIVERSITY OF TEXAS MEDICAL BR GALVESTON · PI LAU, DARYL T · 2005 to 2009
$1.8M
NCRR NIH HHS M01 RR001032NCRR NIH HHS M01-RR-01032NIDDK NIH HHS R01 DK068598NIDDK NIH HHS R01 DK068598-01
6 · The paper itself

Abstract

Using hepatitis C virus (HCV) and interferon (IFN) resistance as a proof of concept, we have devised a new method for calculating the effect of a drug on a viral population, as well as the resistance of the population's individual intrahost variants. By means of next-generation sequencing, HCV variants were obtained from sera collected at nine time points from 16 patients during the first 48 h after injection of IFN-α. IFN-resistance coefficients were calculated for individual variants using changes in their relative frequencies, and for the entire intrahost viral population using changes in viral titer. Population-wide resistance and presence of IFN-resistant variants were highly associated with pegylated IFN-α2a/ribavirin treatment outcome at week 12 (P = 3.78 × 10(-5) and 0.0114, respectively). This new method allows an accurate measurement of resistance based solely on changes in viral titer or the relative frequency of intrahost viral variants during a short observation time.

Indexed as

AlgorithmsAntiviral AgentsDrug Resistance, ViralDrug Therapy, CombinationGenetic VariationHepacivirusHepatitis CHumansInterferon-alphaMolecular Sequence DataPhylogenyPolyethylene GlycolsPopulationPredictive Value of TestsReal-Time Polymerase Chain ReactionRecombinant ProteinsAntiviral AgentsInterferon-alphapeginterferon alfa-2aPolyethylene GlycolsRecombinant ProteinsRibavirinRNA, Viral

Identifiers

PMID24488144
PMCPMC4215939
OpenAlexW1994668539

What OpenQuestion holds

Textmetadata
LicenceTDM
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.