Evidence map›Paper›PMID 19761371›Full record

ArticlePharmacogenomics2009

Cytochrome P450 2C8 pharmacogenetics: a review of clinical studies.

Elizabeth B Daily, Christina L Aquilante

Registry-linked trialOpen access · greenAbstract read
In one paragraph

Article in Pharmacogenomics, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT02360696 (Predictors of Clinical Response to Montelukast in Children With Functional Dyspepsia), which is not on this map. Cited by 56 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
56citing papers in PubMed, 1 pooled it
12.6field-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.

NCT02360696 completednot on this mapstarted 2014, after this paper: background citation

Predictors of Clinical Response to Montelukast in Children With Functional Dyspepsia

TypeobservationalSponsorChildren's Mercy Hospital Kansas CityRan2014 to 2016Enrolled18ConditionsEosinophilia, Dyspepsia
3 · Its place in the literature

Who cites it

56 citing papers in PubMed, 1 synthesis or guideline pooled it, 146 citations in OpenAlex.

  1. Pooled it
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  8. Genetic polymorphisms of CYP2C8 in the Czech Republic.Genetic testing and molecular biomarkers · 2012
    Trial
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  18. Drug metabolism and drug transport of the 100 most prescribed oral drugs.Basic & clinical pharmacology & toxicology · 2022
    Review
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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

2 authors at 1 institution in 1 country.

Elizabeth B DailyDepartment of Pharmaceutical Sciences, University of Colorado Denver, School of Pharmacy, Aurora, CO 80045, USA.
Christina L Aquilante
University of Colorado Denver · US

Funding

Genetic predictors of thiazolidinedione responseK23DK073197 · NIDDK · UNIVERSITY OF COLORADO DENVER · PI AQUILANTE, CHRISTINA L · 2006 to 2010
$601k
NIDDK NIH HHS K23 DK073197
6 · The paper itself

Abstract

Cytochrome P450 (CYP) 2C8 is responsible for the oxidative metabolism of many clinically available drugs from a diverse number of drug classes (e.g., thiazolidinediones, meglitinides, NSAIDs, antimalarials and chemotherapeutic taxanes). The CYP2C8 enzyme is encoded by the CYP2C8 gene, and several common nonsynonymous polymorphisms (e.g., CYP2C8*2 and CYP2C8*3) exist in this gene. The CYP2C8*2 and *3 alleles have been associated in vitro with decreased metabolism of paclitaxel and arachidonic acid. Recently, the influence of CYP2C8 polymorphisms on substrate disposition in humans has been investigated in a number of clinical pharmacogenetic studies. Contrary to in vitro data, clinical data suggest that the CYP2C8*3 allele is associated with increased metabolism of the CYP2C8 substrates, rosiglitazone, pioglitazone and repaglinide. However, the CYP2C8*3 allele has not been associated with paclitaxel pharmacokinetics in most clinical studies. Furthermore, clinical data regarding the impact of the CYP2C8*3 allele on the disposition of NSAIDs are conflicting and no definitive conclusions can be made at this time. The purpose of this review is to highlight these clinical studies that have investigated the association between CYP2C8 polymorphisms and CYP2C8 substrate pharmacokinetics and/or pharmacodynamics in humans. In this review, CYP2C8 clinical pharmacogenetic data are provided by drug class, followed by a discussion of the future of CYP2C8 clinical pharmacogenetic research.

Indexed as

AllelesAnti-Inflammatory Agents, Non-SteroidalAntimalarialsAntineoplastic AgentsAryl Hydrocarbon HydroxylasesCytochrome P-450 CYP2C8Gene FrequencyHumansHydroxymethylglutaryl-CoA Reductase InhibitorsHypoglycemic AgentsOxidation-ReductionPharmaceutical PreparationsPharmacogeneticsPolymorphism, GeneticAnti-Inflammatory Agents, Non-SteroidalAntimalarialsAntineoplastic AgentsAryl Hydrocarbon HydroxylasesCYP2C8 protein, humanCytochrome P-450 CYP2C8Hydroxymethylglutaryl-CoA Reductase InhibitorsHypoglycemic AgentsPharmaceutical Preparations

Identifiers

PMID19761371
PMCPMC2778050
OpenAlexW2109989116

What OpenQuestion holds

Textmetadata
LicenceTDM
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.