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PXR variants and artemisinin use in vietnamese subjects: frequency distribution and impact on the interindividual variability of CYP3A induction by artemisinin

dc.contributor.authorPiedade, Rita
dc.contributor.authorSchaeffeler, Elke
dc.contributor.authorWinter, Stefan
dc.contributor.authorAsimus, Sara
dc.contributor.authorSchwab, Matthias
dc.contributor.authorAshton, Michael
dc.contributor.authorBurk, Oliver
dc.contributor.authorGil, José Pedro
dc.date.accessioned2018-12-07T14:52:31Z
dc.date.available2018-12-07T14:52:31Z
dc.date.issued2012-04
dc.description.abstractArtemisinins induce drug metabolism through the activation of the pregnane X receptor (PXR) in vitro. Here, we report the re-sequencing and genotyping of PXR variants in 75 Vietnamese individuals previously characterized for CYP3A enzyme activity after artemisinin exposure. We identified a total of 31 PXR variants, including 5 novel single nucleotide polymorphisms (SNPs), and we identified significantly different allele frequencies relative to other ethnic groups. A trend of significance was observed between the level of CYP3A4 induction by artemisinin and two PXR variants, the 8118C -> T (Y328Y) and 10719A -> G variants.
dc.description.sponsorshipStyrelsen for Internationellt Utvecklingssamarbete (SIDA), Sweden [SWE-2009-165]; Karolinska Institutet Fond; ICEEPHA (Tubingen-Stuttgart, Germany) [2009-10-0-0]; Federal Ministry for Education and Research (BMBF) (Berlin, Germany) [03 IS 2061C]; DFG [KE 1629/1-1]; Robert Bosch Foundation, Stuttgart, Germany; Fundacao para a Ciencia e Tecnologia, Ministerio da Ciencia e Ensino Superior, Portugal; European and Developing Countries Clinical Trials Partnership (EDCTP)
dc.description.versioninfo:eu-repo/semantics/publishedVersion
dc.identifier.doi10.1128/AAC.06009-11
dc.identifier.issn0066-4804
dc.identifier.urihttp://hdl.handle.net/10400.1/11104
dc.language.isoeng
dc.peerreviewedyes
dc.publisherAmerican Society for Microbiology
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.subjectPregnane-X-receptor
dc.subjectSingle-nucleotide polymorphisms
dc.subjectConstitutive-androstane-receptor
dc.subjectInflammatory-bowel-disease
dc.subjectFalciparum-malaria
dc.subjectGene
dc.subjectAssociation
dc.subjectPharmacokinetics
dc.subjectPharmacogenetics
dc.subjectCytochrome-P450
dc.titlePXR variants and artemisinin use in vietnamese subjects: frequency distribution and impact on the interindividual variability of CYP3A induction by artemisinin
dc.typejournal article
dspace.entity.typePublication
oaire.citation.endPage2157
oaire.citation.issue4
oaire.citation.startPage2153
oaire.citation.titleAntimicrobial Agents and Chemotherapy
oaire.citation.volume56
person.familyNameGil
person.givenNameJosé Pedro
person.identifier.ciencia-idD01A-B30E-BCD5
person.identifier.orcid0000-0002-6107-9379
person.identifier.scopus-author-id7201625436
rcaap.rightsopenAccess
rcaap.typearticle
relation.isAuthorOfPublicationcb728715-0e4c-4ae5-9e21-b6a8f35a8313
relation.isAuthorOfPublication.latestForDiscoverycb728715-0e4c-4ae5-9e21-b6a8f35a8313

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