Association between CYP2A6 genotypes and smoking behavior in Lebanese smokers

dc.contributor.authorFarra, Chantal G.
dc.contributor.authorAssaf, Nada P.
dc.contributor.authorKaraky, Nathalie M.
dc.contributor.authorDiab, Sara
dc.contributor.authorZaatari, Ghazi S.
dc.contributor.authorCortas, Najwa K.
dc.contributor.authorDaher, Rose T.
dc.contributor.departmentPathology and Laboratory Medicine
dc.contributor.facultyFaculty of Medicine (FM)
dc.contributor.institutionAmerican University of Beirut
dc.date.accessioned2025-01-24T12:10:05Z
dc.date.available2025-01-24T12:10:05Z
dc.date.issued2020
dc.description.abstractIntroduction: With the absence of effective reinforcement of tobacco control laws in the country, the Lebanese population has been vulnerable to the health burden of smoking. Smoking and quitting behaviors are influenced by genetic factors, mainly CYP2A6 polymorphisms. To date, the assessment of the genetic profile and its effect on the behavior of Lebanese smokers has not yet been studied. The aim of this study was to determine the CYP2A6 polymorphisms and its relation to smoking and quitting behavior in a cohort of Lebanese smokers. Methods: Healthy adult Lebanese smokers were recruited from the American University of Beirut and its Medical Center. Their nicotine metabolite (NM) levels and CYP2A6 alleles (2, 4, 9 and 12) were determined. The smoking behavior, Nicotine Dependence Score (NDS) and quitting behavior of the participants were assessed after filling a “smoking assessment questionnaire”. Results: 53 healthy adult smokers participated in our study (M: F = 4:1, median age = 38.47 +/− 14.15 years). Mutated CYP* 2 was present in 33.9% (18/53 cases), CYP* 4 in 11.3% (6/53 cases), CYP* 9 in 100% (53/53 cases) and CYP* 12 in 86.7% (46/53 cases). Slow metabolizers constituted 90.6% of our group while 9.4% were intermediate metabolizers. Slow metabolizers smoked a smaller number of cigarettes per day (CPD) (median = 15 CPD vs 25 CPD) and had higher NM levels (median = 23 ng/mL vs 10 ng/mL or undetectable) than intermediate metabolizers. A statistically significant correlation with NDS and quitting behavior was not found in either group. Conclusion: In this first study from Lebanon, a unique distribution of CYP2A6 alleles (high prevalence of CYP2A6*9 and CYP2A6*12) was detected. In accordance with previously published data, slow metabolizers smoked a lower number of CPD and had higher NM levels in their serum. Larger studies are required to fully elucidate the CYP2A6 polymorphisms of Lebanese smokers and include them in personalized smoking cessation programs. © 2019 Elsevier B.V.
dc.identifier.doihttps://doi.org/10.1016/j.mgene.2019.100616
dc.identifier.eid2-s2.0-85073817814
dc.identifier.urihttp://hdl.handle.net/10938/32251
dc.language.isoen
dc.publisherElsevier B.V.
dc.relation.ispartofMeta Gene
dc.sourceScopus
dc.subjectCigarette smoking
dc.subjectGenetic variation
dc.subjectGenetics of smoking
dc.subjectNicotine metabolism
dc.subjectPharmacogenetics
dc.subjectSnp
dc.subjectCytochrome p450 2a6
dc.subjectNicotine
dc.subjectNicotine gum
dc.subjectAdult
dc.subjectAged
dc.subjectAllele
dc.subjectArticle
dc.subjectBehavior disorder assessment
dc.subjectCohort analysis
dc.subjectFemale
dc.subjectGene mutation
dc.subjectGenetic association
dc.subjectGenetic polymorphism
dc.subjectGenetic profile
dc.subjectGenotype
dc.subjectHuman
dc.subjectLebanese
dc.subjectMajor clinical study
dc.subjectMale
dc.subjectMetabolite
dc.subjectNicotine replacement therapy
dc.subjectPriority journal
dc.subjectScoring system
dc.subjectSmoking
dc.subjectSmoking cessation
dc.subjectSmoking habit
dc.subjectTobacco dependence
dc.titleAssociation between CYP2A6 genotypes and smoking behavior in Lebanese smokers
dc.typeArticle

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