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dc.contributor.authorChorlian, David B
dc.contributor.authorRangaswamy, Madhavi
dc.contributor.authorManz, Niklas
dc.contributor.authorWang, Jen-Chyong
dc.contributor.authorDick, Danielle
dc.contributor.authorAlmasy, Laura
dc.contributor.authorBauer, Lance
dc.contributor.authorBucholz, Kathleen
dc.contributor.authorForoud, Tatiana
dc.contributor.authorHesselbrock, Victor
dc.contributor.authorKang, Sun J
dc.contributor.authorKramer, John
dc.contributor.authorKuperman, Sam
dc.contributor.authorNurnberger, John
dc.contributor.authorRice, John
dc.contributor.authorSchuckit, Marc
dc.contributor.authorTischfield, Jay
dc.contributor.authorEdenberg, Howard J
dc.contributor.authorGoate, Alison
dc.contributor.authorBierut, Laura
dc.contributor.authorPorjesz, Bernice
dc.date.accessioned2023-01-23T20:41:19Z
dc.date.available2023-01-23T20:41:19Z
dc.date.issued2013-08-21
dc.identifier.citationChorlian DB, Rangaswamy M, Manz N, Wang JC, Dick D, Almasy L, Bauer L, Bucholz K, Foroud T, Hesselbrock V, Kang SJ, Kramer J, Kuperman S, Nurnberger J Jr, Rice J, Schuckit M, Tischfield J, Edenberg HJ, Goate A, Bierut L, Porjesz B. Genetic and neurophysiological correlates of the age of onset of alcohol use disorders in adolescents and young adults. Behav Genet. 2013 Sep;43(5):386-401. doi: 10.1007/s10519-013-9604-z. Epub 2013 Aug 21. PMID: 23963516; PMCID: PMC4110722.en_US
dc.identifier.eissn1573-3297
dc.identifier.doi10.1007/s10519-013-9604-z
dc.identifier.pmid23963516
dc.identifier.urihttp://hdl.handle.net/20.500.12648/8150
dc.description.abstractDiscrete time survival analysis was used to assess the age-specific association of event-related oscillations (EROs) and CHRM2 gene variants on the onset of regular alcohol use and alcohol dependence. The subjects were 2,938 adolescents and young adults ages 12-25. Results showed that the CHRM2 gene variants and ERO risk factors had hazards which varied considerably with age. The bulk of the significant age-specific associations occurred in those whose age of onset was under 16. These associations were concentrated in those subjects who at some time took an illicit drug. These results are consistent with studies which associate greater rates of alcohol dependence among those who begin drinking at an early age. The age specificity of the genetic and neurophysiological factors is consistent with recent studies of adolescent brain development, which locate an interval of heightened vulnerability to substance use disorders in the early to mid teens.
dc.language.isoenen_US
dc.relation.urlhttps://link.springer.com/article/10.1007/s10519-013-9604-zen_US
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 International*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/*
dc.titleGenetic and neurophysiological correlates of the age of onset of alcohol use disorders in adolescents and young adults.en_US
dc.typeArticle/Reviewen_US
dc.source.journaltitleBehavior geneticsen_US
dc.source.volume43
dc.source.issue5
dc.source.beginpage386
dc.source.endpage401
dc.source.countryUnited States
dc.source.countryUnited States
dc.source.countryUnited States
dc.source.countryUnited States
dc.source.countryUnited States
dc.description.versionAMen_US
refterms.dateFOA2023-01-23T20:41:19Z
html.description.abstractDiscrete time survival analysis was used to assess the age-specific association of event-related oscillations (EROs) and CHRM2 gene variants on the onset of regular alcohol use and alcohol dependence. The subjects were 2,938 adolescents and young adults ages 12-25. Results showed that the CHRM2 gene variants and ERO risk factors had hazards which varied considerably with age. The bulk of the significant age-specific associations occurred in those whose age of onset was under 16. These associations were concentrated in those subjects who at some time took an illicit drug. These results are consistent with studies which associate greater rates of alcohol dependence among those who begin drinking at an early age. The age specificity of the genetic and neurophysiological factors is consistent with recent studies of adolescent brain development, which locate an interval of heightened vulnerability to substance use disorders in the early to mid teens.
dc.description.institutionSUNY Downstateen_US
dc.description.departmentHenri Begleiter Neurodynamics Laboratoryen_US
dc.description.degreelevelN/Aen_US
dc.identifier.journalBehavior genetics


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