Genome-wide association studies identify genetic loci related to alcohol consumption in Korean men

被引:87
|
作者
Baik, Inkyung [2 ]
Cho, Nam H. [3 ]
Kim, Seong Hwan
Han, Bok-Ghee [4 ]
Shin, Chol [1 ,5 ]
机构
[1] Korea Univ, Ansan Hosp, Dept Internal Med, Div Pulm & Crit Care Med, Ansan 425707, South Korea
[2] Kookmin Univ, Dept Foods & Nutr, Coll Nat Sci, Seoul, South Korea
[3] Ajou Univ, Sch Med, Dept Prevent Med, Suwon 441749, South Korea
[4] Natl Inst Hlth, Ctr Genome Sci, Seoul, South Korea
[5] Korea Univ, Ansan Hosp, Inst Human Genom Study, Ansan 425707, South Korea
来源
关键词
SUSCEPTIBILITY LOCI; AFFECTIVE-DISORDER; DEPENDENCE; LINKAGE; ADDICTION; REGION; ALDH2; RISK; POPULATIONS; PHENOTYPE;
D O I
10.3945/ajcn.110.001776
中图分类号
R15 [营养卫生、食品卫生]; TS201 [基础科学];
学科分类号
100403 ;
摘要
Background: Genome-wide association (GWA) studies regarding the quantitative trait of alcohol consumption are limited. Objective: The objective of the study was to explore genetic loci associated with the amount of alcohol consumed. Design: We conducted a GWA study with discovery data on single nucleotide polymorphisms (SNPs) for 1721 Korean male drinkers aged 40-69 y who were included in an urban population-based cohort. Another sample that comprised 1113 male drinkers who were from an independent cohort enrolled in a rural area served as a resource for replication. At baseline (18 June 2001 through 29 January 2003), members of both cohorts provided information on average daily alcohol consumptions, and their DNA samples were collected for genotyping. Results: We tested 315,914 SNPs of discovery data by using multivariate linear regression analysis adjusted for age and smoking, and 12 SNPs on chromosome 12q24 had genome-wide significant associations with alcohol consumption; adjusted P values by using Bonferroni correction were 1.6 x 10(-5) through 5.8 x 10(-46). We observed most SNPs in intronic regions and showed that the genes that harbor SNPs were C12orf51, CCDC63, MYL2, OAS3, CUX2, and RPH3A. In particular, signals in or near C12orf51, CCDC63, and MYL2 were successfully replicated in the test for 317,951 SNPs; rs2074356 in C12orf51 was in high linkage disequilibrium with SNPs in ALDH2, but other SNPs were not. Conclusions: In a GWA study, we identified loci and alleles highly associated with alcohol consumption. The findings suggest the need for further investigations on the genetic propensity for drinking excessive amounts of alcohol. Am J Clin Nutr 2011; 93: 809-16.
引用
收藏
页码:809 / 816
页数:8
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