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dc.contributor.author김미경-
dc.date.accessioned2017-11-28T04:55:18Z-
dc.date.available2017-11-28T04:55:18Z-
dc.date.issued2016-02-
dc.identifier.citationPLOS ONE, v. 11, NO 2, Article number e0149321, Page. 1-14en_US
dc.identifier.issn1932-6203-
dc.identifier.urihttp://journals.plos.org/plosone/article?id=10.1371/journal.pone.0149321-
dc.identifier.urihttp://hdl.handle.net/20.500.11754/31906-
dc.description.abstractPreviously, genetic polymorphisms of C12orf51 (HECTD4) (rs2074356 and/or rs11066280) have been shown to be related to alcohol consumption and type 2 diabetes (T2D). This study aimed to prospectively examine whether C12orf51 had an interaction with or independent effect on alcohol consumption and the risk of T2D. The present study included 3,244 men and 3,629 women aged 40 to 69 years who participated in the Korean Genome and Epidemiology Study (KoGES)_Ansan and Ansung Study. Cox proportional hazards models were used to estimate HRs and 95% CIs for T2D. rs2074356 and rs11066280 were associated with the risk of T2D after adjusting for alcohol consumption (rs2074356 for AA: HR = 0.39 and 95% CI = 0.17-0.87 in men, and HR = 0.36 and 95% CI = 0.13-0.96 in women; rs11066280 for AA: HR = 0.44 and 95% CI = 0.23-0.86 in men, and HR = 0.39 and 95% CI = 0.16-0.94 in women). We identified that the association of each variant (rs2074356 and rs11065756) in C12orf51 was nearly unchanged after adjusted for alcohol consumption. Therefore, the association of 2 SNPs in C12orf51 with diabetes may not be mediated by alcohol use. There was no interaction effect between alcohol consumption and the SNPs with T2D. However, even in never-drinkers, minor allele homozygote strongly influenced T2D risk reduction (rs2074356 for AA: HR = 0.35, 95% CI = 0.14-0.90, and p-trend = 0.0035 in men and HR = 0.34, 95% CI = 0.13-0.93, and p-trend = 0.2348 in women; rs11066280 for AA: HR = 0.36, 95% CI = 0.16-0.82, and p-trend = 0.0014 in men and HR = 0.39, 95% CI = 0.16-0.95, and p-trend = 0.3790 in women), while alcohol consumption did not influence the risk of T2D within each genotype. rs2074356 and rs11066280 in or near C12orf51, which is related to alcohol drinking behavior, may longitudinally decrease the risk of T2D, but not through regulation of alcohol consumption.en_US
dc.description.sponsorshipThis research was supported by a fund (HD14B0005) by Research of Korea Centers for Disease Control and Prevention and MKK received the funding. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript. This study was provided with biospecimens and data from the Korean Genome Analysis Projects (4845-301), the Korean Genome and Epidemiology (4845-302) and Korea Biobank Project (4851-307, KBP-2014-000) that were supported by the Korea Centers for Disease Control & Prevention, Republic of Korea.en_US
dc.language.isoenen_US
dc.publisherPUBLIC LIBRARY SCIENCEen_US
dc.subjectALDEHYDE DEHYDROGENASE GENOTYPESen_US
dc.subjectGENOME-WIDE ASSOCIATIONen_US
dc.subjectDRINKING BEHAVIORen_US
dc.subjectINSULIN-RESISTANCEen_US
dc.subjectSYNTAXIN 8en_US
dc.subjectALDH2en_US
dc.subjectRISKen_US
dc.subjectMETAANALYSISen_US
dc.subjectJAPANESEen_US
dc.subjectCHINESEen_US
dc.titleNo Interaction with Alcohol Consumption, but Independent Effect of C12orf51 (HECTD4) on Type 2 Diabetes Mellitus in Korean Adults Aged 40-69 Years: The KoGES_Ansan and Ansung Studyen_US
dc.typeArticleen_US
dc.relation.no2-
dc.relation.volume11-
dc.identifier.doi10.1371/journal.pone.0149321-
dc.relation.page1-14-
dc.relation.journalPLOS ONE-
dc.contributor.googleauthorKim, Jihye-
dc.contributor.googleauthorOh, Bermseok-
dc.contributor.googleauthorLim, Ji Eun-
dc.contributor.googleauthorKim, Mi Kyung-
dc.relation.code2016007072-
dc.sector.campusS-
dc.sector.daehakCOLLEGE OF MEDICINE[S]-
dc.sector.departmentDEPARTMENT OF MEDICINE-
dc.identifier.pidkmkkim-


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