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Association of a single nucleotide polymorphism in neuronal acetylcholine receptor subunit alpha 5 (CHRNA5) with smoking status and with ‘pleasurable buzz’ during early experimentation with smoking

dc.contributor.authorSherva, Richarden_US
dc.contributor.authorWilhelmsen, Kirken_US
dc.contributor.authorPomerleau, Cynthia S.en_US
dc.contributor.authorChasse, Scott A.en_US
dc.contributor.authorRice, John P.en_US
dc.contributor.authorSnedecor, Sandy M.en_US
dc.contributor.authorBierut, Laura J.en_US
dc.contributor.authorNeuman, Rosalind J.en_US
dc.contributor.authorPomerleau, Ovide F.en_US
dc.date.accessioned2010-06-01T21:46:36Z
dc.date.available2010-06-01T21:46:36Z
dc.date.issued2008-09en_US
dc.identifier.citationSherva, Richard; Wilhelmsen, Kirk; Pomerleau, Cynthia S.; Chasse, Scott A.; Rice, John P.; Snedecor, Sandy M.; Bierut, Laura J.; Neuman, Rosalind J.; Pomerleau, Ovide F. (2008). "Association of a single nucleotide polymorphism in neuronal acetylcholine receptor subunit alpha 5 (CHRNA5) with smoking status and with ‘pleasurable buzz’ during early experimentation with smoking." Addiction 103(9): 1544-1552. <http://hdl.handle.net/2027.42/74818>en_US
dc.identifier.issn0965-2140en_US
dc.identifier.issn1360-0443en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/74818
dc.identifier.urihttp://www.ncbi.nlm.nih.gov/sites/entrez?cmd=retrieve&db=pubmed&list_uids=18783506&dopt=citationen_US
dc.description.abstractAims  To extend the previously identified association between a single nucleotide polymorphism (SNP) in neuronal acetylcholine receptor subunit alpha-5 (CHRNA5) and nicotine dependence to current smoking and initial smoking-experience phenotypes. Design, setting, participants  Case–control association study with a community-based sample, comprising 363 Caucasians and 72 African Americans (203 cases, 232 controls). Measurements  Cases had smoked ≥ five cigarettes/day for ≥ 5 years and had smoked at their current rate for the past 6 months. Controls had smoked between one and 100 cigarettes in their life-time, but never regularly. Participants also rated, retrospectively, pleasurable and displeasurable sensations experienced when they first smoked. We tested for associations between smoking phenotypes and the top 25 SNPs tested for association with nicotine dependence in a previous study. Findings  A non-synonymous coding SNP in CHRNA5, rs16969968, was associated with case status [odds ratio (OR) = 1.5, P  = 0.01] and, in Caucasians, with experiencing a pleasurable rush or buzz during the first cigarette (OR = 1.6, P  = 0.01); these sensations were associated highly with current smoking (OR = 8.2, P  = 0.0001). Conclusions  We replicated the observation that the minor allele of rs16969968 affects smoking behavior, and extended these findings to sensitivity to smoking effects upon experimentation. While the ability to test genetic associations was limited by sample size, the polymorphism in the CHRNA5 subunit was shown to be associated significantly with enhanced pleasurable responses to initial cigarettes in regular smokers in an a priori test. The findings suggest that phenotypes related to subjective experiences upon smoking experimentation may mediate the development of nicotine dependence.en_US
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dc.publisherBlackwell Publishing Ltden_US
dc.rightsJournal compilation © 2008 Society for the Study of Addictionen_US
dc.subject.otherCase–Control Designen_US
dc.subject.otherChromosome 15en_US
dc.subject.otherEarly Smoking Experiencesen_US
dc.subject.otherNicotinic Alpha-5 Receptor Subuniten_US
dc.subject.otherSingle Nucleotide Polymorphisms (SNPs)en_US
dc.subject.otherSmokers and Never-smokersen_US
dc.titleAssociation of a single nucleotide polymorphism in neuronal acetylcholine receptor subunit alpha 5 (CHRNA5) with smoking status and with ‘pleasurable buzz’ during early experimentation with smokingen_US
dc.typeArticleen_US
dc.subject.hlbsecondlevelPsychiatryen_US
dc.subject.hlbsecondlevelPublic Healthen_US
dc.subject.hlbtoplevelHealth Sciencesen_US
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationumDepartment of Psychiatry, University of Michigan, Ann Arbor, MI, USA anden_US
dc.contributor.affiliationotherDepartment of Psychiatry, Washington University School of Medicine, St Louis, MO, USA,en_US
dc.contributor.affiliationotherDepartment of Genetics and Neurology, Carolina Center for Genome Sciences, Chapel Hill, NC, USA,en_US
dc.contributor.affiliationotherDepartment of Biochemistry and Biophysics, University of North Carolina, Chapel Hill, NC, USAen_US
dc.identifier.pmid18783506en_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/74818/1/j.1360-0443.2008.02279.x.pdf
dc.identifier.doi10.1111/j.1360-0443.2008.02279.xen_US
dc.identifier.sourceAddictionen_US
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dc.owningcollnameInterdisciplinary and Peer-Reviewed


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