The pharmacogenetics of drug metabolizing enzymes in the Lebanese population

dc.contributor.authorOssaily, Safaa
dc.contributor.authorKhoueiry-Zgheib, Nathalie
dc.contributor.departmentPharmacology and Toxicology
dc.contributor.facultyFaculty of Medicine (FM)
dc.contributor.institutionAmerican University of Beirut
dc.date.accessioned2025-01-24T11:39:27Z
dc.date.available2025-01-24T11:39:27Z
dc.date.issued2014
dc.description.abstractDrug metabolizing enzymes (DMEs) play a major role in the metabolism and final elimination of most drugs and xenobiotics from the body. Both phase I and phase II enzymes are highly polymorphic. Most studies on the pharmacogenetics (PGx) of DMEs and its influence on interindividual variability have been conducted in Western countries. Middle Easterners, however, may have a different genetic makeup and may be exposed to different environmental factors when compared with their Western counterparts. Thus, results obtained in Western populations cannot be extrapolated to the population of the Middle East, and it is important to examine and document PGx differences and influences within the Middle Eastern population as there have been very little published data from this region. Herein, we provide an update on the genetic polymorphisms of DMEs that were studied in Lebanon and their impact on drug toxicity and efficacy. It is hoped that with more time, additional funds, and perseverance, the PGx of DMEs in Lebanon picks up and becomes closer in quantity and quality to that in the West.
dc.identifier.doihttps://doi.org/10.1515/dmdi-2013-0058
dc.identifier.eid2-s2.0-84904182091
dc.identifier.pmid24413215
dc.identifier.urihttp://hdl.handle.net/10938/29230
dc.language.isoen
dc.publisherWalter de Gruyter GmbH
dc.relation.ispartofDrug Metabolism and Drug Interactions
dc.sourceScopus
dc.subjectCyps
dc.subjectDrug metabolizing enzymes (dmes)
dc.subjectLebanon
dc.subjectPharmacogenetics
dc.subjectArabs
dc.subjectCytochrome p-450 cyp2b6
dc.subjectGlutathione transferase
dc.subjectHumans
dc.subjectInactivation, metabolic
dc.subjectPharmaceutical preparations
dc.subjectVitamin k epoxide reductases
dc.subjectAbc transporter g1
dc.subjectAcenocoumarol
dc.subjectAnticoagulant agent
dc.subjectBreast cancer resistance protein
dc.subjectCalcifediol
dc.subjectClopidogrel
dc.subjectCoumarin anticoagulant
dc.subjectCyclophosphamide
dc.subjectCytochrome p450 1a2
dc.subjectCytochrome p450 2c19
dc.subjectCytochrome p450 2c9
dc.subjectCytochrome p450 2d6
dc.subjectDocetaxel
dc.subjectDrug metabolizing enzyme
dc.subjectGlutathione transferase m1
dc.subjectGlutathione transferase t1
dc.subjectMethotrexate
dc.subjectMultidrug resistance associated protein 6
dc.subjectTamoxifen
dc.subjectWarfarin
dc.subjectCytochrome p450 2b6
dc.subjectDrug
dc.subjectVitamin k epoxide reductase
dc.subjectArtery thrombosis
dc.subjectArtificial neural network
dc.subjectAutoimmune disease
dc.subjectBreast cancer
dc.subjectCancer combination chemotherapy
dc.subjectDrug absorption
dc.subjectDrug distribution
dc.subjectDrug efficacy
dc.subjectDrug elimination
dc.subjectDrug metabolism
dc.subjectEstrogen receptor positive breast cancer
dc.subjectGene frequency
dc.subjectGenetic polymorphism
dc.subjectGenotype
dc.subjectHigh throughput sequencing
dc.subjectHuman
dc.subjectInternational normalized ratio
dc.subjectLoss of function mutation
dc.subjectReview
dc.subjectSingle nucleotide polymorphism
dc.subjectThrombocyte aggregation
dc.subjectVein thrombosis
dc.subjectVitamin d deficiency
dc.subjectArab
dc.subjectDrug inactivation
dc.subjectGenetics
dc.subjectMetabolism
dc.titleThe pharmacogenetics of drug metabolizing enzymes in the Lebanese population
dc.typeReview

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