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Cited 17 time in webofscience Cited 22 time in scopus
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Association of CLOCK, ARNTL, PER2, and GNB3 polymorphisms with diurnal preference in a Korean population

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dc.contributor.authorSong, Hye-Min-
dc.contributor.authorCho, Chul-Hyun-
dc.contributor.authorLee, Heon-Jeong-
dc.contributor.authorMoon, Joung Ho-
dc.contributor.authorKang, Seung-Gul-
dc.contributor.authorYoon, Ho-Kyoung-
dc.contributor.authorPark, Young-Min-
dc.contributor.authorKim, Leen-
dc.date.available2020-02-28T06:43:14Z-
dc.date.created2020-02-06-
dc.date.issued2016-11-
dc.identifier.issn0742-0528-
dc.identifier.urihttps://scholarworks.bwise.kr/gachon/handle/2020.sw.gachon/9685-
dc.description.abstractPolymorphisms in human circadian genes are potential genetic markers that affect diurnal preference in several populations. In this study, we evaluated whether four polymorphisms in circadian genes CLOCK, ARNTL, PER2, and GNB3 were associated with diurnal preference in a Korean population. In all, 499 healthy subjects were genotyped for four functional polymorphisms in CLOCK, ARNTL, PER2, and GNB3. Composite scale of morningness (CSM) was applied to measure phenotype patterns of human diurnal preference. In addition, three subscale scores, i.e. "morningness," "activity planning," and "morning alertness," were extracted from the CSM. No significant associations were observed between CSM scores and CLOCK (rs1801260) genotype or T allele carrier status, CSM scores and ARNTL (rs2278749) C allele carrier status, and CSM scores and GNB3 (rs5443) genotype or C allele carrier status. However, total CSM scores and scores of its subscales were significantly associated with PER2 (rs934945) genotype (p = 0.010, p = 0.018, and p = 0.005 for total, morningness, and activity planning, respectively) and G allele carrier status (p = 0.003, p = 0.005, and p = 0.002 for total, morningness, and activity planning, respectively). The best model result obtained by performing multifactor dimensionality reduction analysis (chi(2) = 11.2798, p = 0.0008) indicated that interaction among C/T single nucleotide polymorphism (SNP) in ARNTL, C/T SNP in GNB3, and G/A SNP in PER2 synergistically affected the risk associated with diurnal preference toward eveningness. These results suggest that circadian gene PER2 is associated with diurnal preference in healthy Korean population. Although polymorphisms in ARNTL and GNB3 were not significantly associated with diurnal preference, their interactions with the polymorphism in PER2 may synergistically increase the risk of diurnal preference toward eveningness.-
dc.language영어-
dc.language.isoen-
dc.publisherTAYLOR & FRANCIS INC-
dc.relation.isPartOfCHRONOBIOLOGY INTERNATIONAL-
dc.titleAssociation of CLOCK, ARNTL, PER2, and GNB3 polymorphisms with diurnal preference in a Korean population-
dc.typeArticle-
dc.type.rimsART-
dc.description.journalClass1-
dc.identifier.wosid000388746800015-
dc.identifier.doi10.1080/07420528.2016.1231199-
dc.identifier.bibliographicCitationCHRONOBIOLOGY INTERNATIONAL, v.33, no.10, pp.1455 - 1463-
dc.description.isOpenAccessN-
dc.identifier.scopusid2-s2.0-84988663685-
dc.citation.endPage1463-
dc.citation.startPage1455-
dc.citation.titleCHRONOBIOLOGY INTERNATIONAL-
dc.citation.volume33-
dc.citation.number10-
dc.contributor.affiliatedAuthorKang, Seung-Gul-
dc.type.docTypeArticle-
dc.subject.keywordAuthorDiurnal preference-
dc.subject.keywordAuthorCLOCK-
dc.subject.keywordAuthorARNTL-
dc.subject.keywordAuthorPER2-
dc.subject.keywordAuthorGNB3-
dc.subject.keywordAuthorpolymorphism-
dc.subject.keywordPlusMAMMALIAN CIRCADIAN CLOCK-
dc.subject.keywordPlusSEASONAL AFFECTIVE-DISORDER-
dc.subject.keywordPlusSLEEP-PHASE SYNDROME-
dc.subject.keywordPlusC825T POLYMORPHISM-
dc.subject.keywordPlusGENE POLYMORPHISM-
dc.subject.keywordPlusLENGTH POLYMORPHISM-
dc.subject.keywordPlusBIPOLAR DISORDER-
dc.subject.keywordPlusRHYTHM-
dc.subject.keywordPlusDISEASE-
dc.subject.keywordPlusMORNINGNESS-
dc.relation.journalResearchAreaLife Sciences & Biomedicine - Other Topics-
dc.relation.journalResearchAreaPhysiology-
dc.relation.journalWebOfScienceCategoryBiology-
dc.relation.journalWebOfScienceCategoryPhysiology-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
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