Evidence map›Paper›PMID 27349952›Full record

ArticleJournal of clinical pharmacology2017

Variant Inosine Triphosphatase Phenotypes Are Associated With Increased Ribavirin Triphosphate Levels.

Leah C Jimmerson, Thomas J Urban, Aimee Truesdale, Fafa Baouchi-Mokrane, Shyam Kottilil, Eric G Meissner, Zayani Sims, Jacob A Langness, Ariel Hodara, Christina L Aquilante and 1 more

Open access · greenAbstract read
In one paragraph

Article in Journal of clinical pharmacology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
1.1field-weighted citation impact, top 22% 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

4 citing papers in PubMed, 9 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. 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 6 institutions in 2 countries.

Leah C JimmersonSkaggs School of Pharmacy and Pharmaceutical Sciences, University of Colorado Denver, Aurora, Colorado.
Thomas J UrbanDivision of Pharmacotherapy and Experimental Therapeutics, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina.
Aimee TruesdaleDenver Health Medical Center, Denver, Colorado.
Fafa Baouchi-MokraneDenver Health Medical Center, Denver, Colorado.
Shyam KottililDivision of Clinical Care and Research, Institute of Human Virology, University of Maryland, Baltimore, Maryland.
Eric G MeissnerDivision of Infectious Diseases, Department of Microbiology and Immunology, Medical University of South Carolina, Charleston, South Carolina.
Zayani SimsCritical Care Medicine Department, Clinical Center, National Institute of Health, Bethesda, Maryland.
Jacob A LangnessSkaggs School of Pharmacy and Pharmaceutical Sciences, University of Colorado Denver, Aurora, Colorado.
Ariel HodaraSkaggs School of Pharmacy and Pharmaceutical Sciences, University of Colorado Denver, Aurora, Colorado.
Christina L AquilanteSkaggs School of Pharmacy and Pharmaceutical Sciences, University of Colorado Denver, Aurora, Colorado.
Jennifer J KiserSkaggs School of Pharmacy and Pharmaceutical Sciences, University of Colorado Denver, Aurora, Colorado.
University of Montana · USNational Institutes of Health Clinical Center · USUniversity of Colorado Denver · USDenver Health Medical Center · USInstitute of Human Virology · NGUniversity of North Carolina at Chapel Hill · US

Funding

DC Partnership for HIV/AIDS Progress (DC PFAP)ZIACL009010 · CLC · CLINICAL CENTER · PI MASUR, HENRY · 2010 to 2025
$0k
Intramural NIH HHS ZIA CL009010
6 · The paper itself

Abstract

Individuals with lower inosine triphosphatase (ITPA) enzyme activity have a reduced likelihood of experiencing hemolytic anemia during hepatitis C virus (HCV) treatment containing ribavirin (RBV). Because ITPA degrades purines and RBV is a purine analogue, it is conceivable that ITPA activity may affect intracellular RBV concentrations. Here we assessed the association between ITPA activity phenotype and concentrations of RBV triphosphate (RBV-TP) in red blood cells (RBCs) during HCV treatment. RBV-TP was quantified in the RBCs of 177 HCV-infected individuals at a median (range) of 84 (19 to 336) days into HCV treatment that included RBV. Mean (SD) RBV-TP concentrations were 92.8 (51.6), 101.3 (53.5), 184.8 (84.5), and 197.7 (64.6) pmol/10

Indexed as

PhenotypeAdultCohort StudiesFemaleHepatitis C, ChronicHumansInosine TriphosphataseMaleMiddle AgedPharmacogenomic VariantsPyrophosphatasesRibavirinInosine TriphosphatasePyrophosphatasesRibavirinhemoglobin declineIntracellular pharmacologyITPA activityPharmacogenetics/PharmacogenomicsRibavirin triphosphateSNPs

Identifiers

PMID27349952
PMCPMC10725569
OpenAlexW2462556703

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.