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DRD3 Gene rs6280 Polymorphism May Be Associated with Alcohol Dependence Overall and with Lesch Type I Alcohol Dependence in Koreans

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dc.contributor.authorKang, Seung-Gul-
dc.contributor.authorLee, Bun-Hee-
dc.contributor.authorLee, Jun-Seok-
dc.contributor.authorChai, Young Gyu-
dc.contributor.authorKo, Kwang-Pil-
dc.contributor.authorLee, Heon-Jeong-
dc.contributor.authorHan, Dal Mu Ri-
dc.contributor.authorJi, Hong-
dc.contributor.authorJang, Gyeong-Ho-
dc.contributor.authorShin, Hye Eun-
dc.date.available2020-02-28T22:41:37Z-
dc.date.created2020-02-06-
dc.date.issued2014-06-
dc.identifier.issn0302-282X-
dc.identifier.urihttps://scholarworks.bwise.kr/gachon/handle/2020.sw.gachon/14036-
dc.description.abstractBackground: Several polymorphisnns of the dopamine D-3 receptor (DRD3) gene are reported to be involved in the susceptibility to alcoholism. Although the DRD3 rs6280 (Ser9-Gly) polymorphism plays an important role in various psychiatric disorders, findings regarding the association between this single-nucleotide polymorphism (SNP) and alcohol dependence (AD) have been inconsistent. Therefore, the present study investigated the association between the DRD3 gene rs6280 polymorphism with AD and Lesch type I AD in Korean subjects. Methods: The DRD3 rs6280 SNP was genotyped in a case-control sample comprising 245 AD patients and 130 healthy controls (HCs). Alcohol Use Disorders Identification Test (AUDIT) scores were also compared relative to genotype in all of the participants. Results: This SNP was significantly associated with both AD overall (chi(2) = 10.09 and p = 0.001, and chi(2) = 10.60 and p = 0.005, for the recessive and additive models, respectively) and with Lesch type I AD (chi(2) = 11.70 and p(r) = 0.001, and chi(2) = 11.70 and p = 0.003, for the recessive and additive models, respectively). The allele frequency differed significantly (chi(2) = 8.45, p = 0.004) between Lesch type I AD and HC subjects. The AUDIT total (F = 6.56, p = 0.011), hazardous alcohol use (F = 7.12, p = 0.008), dependence symptoms (F = 5.10, p = 0.025), and harmful alcohol use (F = 4.83, p = 0.029) scores were significantly higher in those who did not possess the S allele (genotype GG) than in those who did (genotypes SS +/- SG). Conclusions: The findings of this study suggest that the DRD3 rs6280 polymorphism is associated with the development of both AD overall and Lesch type I AD in Koreans. (C) 2014 S. Karger AG, Basel-
dc.language영어-
dc.language.isoen-
dc.publisherKARGER-
dc.relation.isPartOfNEUROPSYCHOBIOLOGY-
dc.titleDRD3 Gene rs6280 Polymorphism May Be Associated with Alcohol Dependence Overall and with Lesch Type I Alcohol Dependence in Koreans-
dc.typeArticle-
dc.type.rimsART-
dc.description.journalClass1-
dc.identifier.wosid000337267300002-
dc.identifier.doi10.1159/000358062-
dc.identifier.bibliographicCitationNEUROPSYCHOBIOLOGY, v.69, no.3, pp.140 - 146-
dc.description.isOpenAccessN-
dc.identifier.scopusid2-s2.0-84899613842-
dc.citation.endPage146-
dc.citation.startPage140-
dc.citation.titleNEUROPSYCHOBIOLOGY-
dc.citation.volume69-
dc.citation.number3-
dc.contributor.affiliatedAuthorKang, Seung-Gul-
dc.contributor.affiliatedAuthorKo, Kwang-Pil-
dc.type.docTypeArticle-
dc.subject.keywordAuthorAlcohol dependence-
dc.subject.keywordAuthorDRD3 gene-
dc.subject.keywordAuthorPolymorphism-
dc.subject.keywordAuthorLesch type I-
dc.subject.keywordAuthorAlcohol Use Disorders Identification Test-
dc.subject.keywordAuthorKoreans-
dc.subject.keywordPlusDOPAMINE D-3 RECEPTOR-
dc.subject.keywordPlusD3 RECEPTOR-
dc.subject.keywordPlusENVIRONMENTAL CONTRIBUTIONS-
dc.subject.keywordPlusPSYCHIATRIC EPIDEMIOLOGY-
dc.subject.keywordPlusSEEKING BEHAVIOR-
dc.subject.keywordPlusNO ASSOCIATION-
dc.subject.keywordPlusANTAGONIST-
dc.subject.keywordPlusSCHIZOPHRENIA-
dc.subject.keywordPlusREINSTATEMENT-
dc.subject.keywordPlusHOMOZYGOSITY-
dc.relation.journalResearchAreaNeurosciences & Neurology-
dc.relation.journalResearchAreaPsychiatry-
dc.relation.journalResearchAreaPsychology-
dc.relation.journalWebOfScienceCategoryNeurosciences-
dc.relation.journalWebOfScienceCategoryPsychiatry-
dc.relation.journalWebOfScienceCategoryPsychology-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
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