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Serotonin transporter promoter polymorphism, peripheral indexes of serotonin function, and personality measures in families with alcoholism

dc.contributor.authorStoltenberg, Scott F.en_US
dc.contributor.authorTwitchell, Geoffrey R.en_US
dc.contributor.authorHanna, Gregory L.en_US
dc.contributor.authorCook, Edwin H.en_US
dc.contributor.authorFitzgerald, Hiram E.en_US
dc.contributor.authorZucker, Robert A.en_US
dc.contributor.authorLittle, Karley Y.en_US
dc.date.accessioned2006-04-19T13:44:42Z
dc.date.available2006-04-19T13:44:42Z
dc.date.issued2002-03-08en_US
dc.identifier.citationStoltenberg, Scott F.; Twitchell, Geoffrey R.; Hanna, Gregory L.; Cook, Edwin H.; Fitzgerald, Hiram E.; Zucker, Robert A.; Little, Karley Y. (2002)."Serotonin transporter promoter polymorphism, peripheral indexes of serotonin function, and personality measures in families with alcoholism." American Journal of Medical Genetics 114(2): 230-234. <http://hdl.handle.net/2027.42/34664>en_US
dc.identifier.issn0148-7299en_US
dc.identifier.issn1096-8628en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/34664
dc.identifier.urihttp://www.ncbi.nlm.nih.gov/sites/entrez?cmd=retrieve&db=pubmed&list_uids=11857587&dopt=citationen_US
dc.description.abstractA functional polymorphism in the regulatory region of the serotonin transporter gene (5-HTTLPR) is considered to be a plausible candidate gene for anxiety-related personality traits and for alcoholism. Empirical support for the association between 5-HTTLPR and psychological traits has been somewhat inconsistent; however, observations of the functional dominance of the low-activity s-allele over the l-allele have been more consistent. When studying the influence of particular genes on psychological traits, it seems useful also to assess more biological intermediate traits that may mediate the effects of those genes on the traits of interest. The present study examined relationships between 5-HTTLPR genotype, whole blood serotonin (5-HT) level, and platelet 5-HT binding in 150 Caucasian subjects from 50 biological families. Individuals with the s-allele had lower average platelet 5-HT binding availability than those with the l/l genotype ( P  < 0.025). Whole blood 5-HT level was not associated with 5-HTTLPR genotype. In adult men, those with the s-allele had higher mean scores on the NEO-FFI personality trait of openness than did those with the l/l genotype ( P  = 0.002). The effect was not statistically significant in women ( P  = 0.42), although it was in the same direction. Our findings do not support an association of 5-HTTLPR genotype with alcoholism diagnosis, alcoholism subtype, or the personality trait of neuroticism. The results of this pilot study suggest that further work should examine the mediation of the genetic effects on personality traits by biochemical measures and their moderation by gender. © 2002 Wiley-Liss, Inc.en_US
dc.format.extent95982 bytes
dc.format.extent3118 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
dc.language.isoen_US
dc.publisherWiley Subscription Services, Inc., A Wiley Companyen_US
dc.subject.otherLife and Medical Sciencesen_US
dc.subject.otherGeneticsen_US
dc.titleSerotonin transporter promoter polymorphism, peripheral indexes of serotonin function, and personality measures in families with alcoholismen_US
dc.typeArticleen_US
dc.rights.robotsIndexNoFollowen_US
dc.subject.hlbsecondlevelGeneticsen_US
dc.subject.hlbtoplevelHealth Sciencesen_US
dc.subject.hlbtoplevelScienceen_US
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationumUniversity of Michigan Addiction Research Center and Department of Psychiatry, University of Michigan, Ann Arbor, Michigan ; University of Michigan Addiction Research Center, 400 East Eisenhower Parkway, Suite 2A, Ann Arbor, MI 48108.en_US
dc.contributor.affiliationumUniversity of Michigan Addiction Research Center and Department of Psychiatry, University of Michigan, Ann Arbor, Michiganen_US
dc.contributor.affiliationumUniversity of Michigan Addiction Research Center and Department of Psychiatry, University of Michigan, Ann Arbor, Michiganen_US
dc.contributor.affiliationumUniversity of Michigan Addiction Research Center and Department of Psychiatry, University of Michigan, Ann Arbor, Michiganen_US
dc.contributor.affiliationotherDepartment of Psychology, Michigan State University, East Lansing, Michigan ; UCLA Integrated Substance Abuse Program, University of California at Los Angeles, Los Angeles, Californiaen_US
dc.contributor.affiliationotherLaboratory of Developmental Neuroscience and Department of Psychiatry, the University of Chicago, Chicago, Illinoisen_US
dc.contributor.affiliationotherDepartment of Psychology, Michigan State University, East Lansing, Michiganen_US
dc.identifier.pmid11857587en_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/34664/1/10187_ftp.pdfen_US
dc.identifier.doihttp://dx.doi.org/10.1002/ajmg.10187en_US
dc.identifier.sourceAmerican Journal of Medical Geneticsen_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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