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全基因组关联研究最大饮酒量。

Genome-wide association studies of maximum number of drinks.

机构信息

Department of Biostatistics and Epidemiology, College of Public Health, East Tennessee State University, Johnson City, TN, USA; Department of Epidemiology and Public Health, Miller School of Medicine, University of Miami, Miami, FL, USA.

出版信息

J Psychiatr Res. 2013 Nov;47(11):1717-24. doi: 10.1016/j.jpsychires.2013.07.013. Epub 2013 Aug 13.

Abstract

Maximum number of drinks (MaxDrinks) defined as "Maximum number of alcoholic drinks consumed in a 24-h period" is an intermediate phenotype that is closely related to alcohol dependence (AD). Family, twin and adoption studies have shown that the heritability of MaxDrinks is approximately 0.5. We conducted the first genome-wide association (GWA) study and meta-analysis of MaxDrinks as a continuous phenotype. 1059 individuals were from the Collaborative Study on the Genetics of Alcoholism (COGA) sample and 1628 individuals were from the Study of Addiction - Genetics and Environment (SAGE) sample. Family sample with 3137 individuals was from the Australian twin-family study of alcohol use disorder (OZALC). Two population-based Caucasian samples (COGA and SAGE) with 1 million single-nucleotide polymorphisms (SNPs) were used for gene discovery and one family-based Caucasian sample was used for replication. Through meta-analysis we identified 162 SNPs associated with MaxDirnks (p < 10(-4)). The most significant association with MaxDrinks was observed with SNP rs11128951 (p = 4.27 × 10(-8)) near SGOL1 gene at 3p24.3. Furthermore, several SNPs (rs17144687 near DTWD2, rs12108602 near NDST4, and rs2128158 in KCNB2) showed significant associations with MaxDrinks (p < 5 × 10(-7)) in the meta-analysis. Especially, 8 SNPs in DDC gene showed significant associations with MaxDrinks (p < 5 × 10(-7)) in the SAGE sample. Several flanking SNPs in above genes/regions were confirmed in the OZALC family sample. In conclusions, we identified several genes/regions associated with MaxDrinks. These findings can improve the understanding about the pathogenesis of alcohol consumption phenotypes and alcohol-related disorders.

摘要

最大饮酒量(MaxDrinks)定义为“24 小时内消耗的最大酒精饮料数量”,是一种与酒精依赖(AD)密切相关的中间表型。家族、双胞胎和收养研究表明,MaxDrinks 的遗传率约为 0.5。我们进行了最大饮酒量作为连续表型的全基因组关联(GWA)研究和荟萃分析。1059 人来自酒精中毒遗传学合作研究(COGA)样本,1628 人来自成瘾遗传学和环境研究(SAGE)样本。来自澳大利亚酒精使用障碍双生子家族研究(OZALC)的 3137 个个体的家族样本。使用两个基于人群的白种人样本(COGA 和 SAGE)和 100 万个单核苷酸多态性(SNP)进行基因发现,一个基于家族的白种人样本用于复制。通过荟萃分析,我们确定了 162 个与 MaxDirnks 相关的 SNP(p < 10(-4))。与 MaxDrinks 相关性最强的是位于 3p24.3 的 SGOL1 基因附近的 SNP rs11128951(p = 4.27 × 10(-8))。此外,在荟萃分析中,rs17144687 附近的 DTWD2、rs12108602 附近的 NDST4 和 KCNB2 中的 rs2128158 等几个 SNP 也与 MaxDrinks 有显著关联(p < 5 × 10(-7))。特别是,SAGE 样本中 DDC 基因中的 8 个 SNP 与 MaxDrinks 有显著关联(p < 5 × 10(-7))。上述基因/区域的几个侧翼 SNP 在 OZALC 家族样本中得到了确认。总之,我们确定了与 MaxDrinks 相关的几个基因/区域。这些发现可以提高对饮酒表型和与酒精相关疾病发病机制的认识。

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本文引用的文献

1
The relationship between rs3779084 in the dopa decarboxylase (DDC) gene and alcohol consumption is mediated by drinking motives in regular smokers.
Alcohol Clin Exp Res. 2012 Jan;36(1):162-70. doi: 10.1111/j.1530-0277.2011.01596.x. Epub 2011 Jul 28.
3
A novel tumor-derived SGOL1 variant causes abnormal mitosis and unstable chromatid cohesion.
Oncogene. 2011 Nov 3;30(44):4453-63. doi: 10.1038/onc.2011.152. Epub 2011 May 2.
4
Mitotic centromeric targeting of HP1 and its binding to Sgo1 are dispensable for sister-chromatid cohesion in human cells.
Mol Biol Cell. 2011 Apr 15;22(8):1181-90. doi: 10.1091/mbc.E11-01-0009. Epub 2011 Feb 23.
5
Copy number variations and primary open-angle glaucoma.
Invest Ophthalmol Vis Sci. 2011 Sep 9;52(10):7122-33. doi: 10.1167/iovs.10-5606. Print 2011.
6
Genome-wide association studies of alcohol dependence and substance use disorders.
Curr Psychiatry Rep. 2011 Apr;13(2):147-55. doi: 10.1007/s11920-011-0176-4.
7
A candidate gene association study of alcohol consumption in young women.
Alcohol Clin Exp Res. 2011 Mar;35(3):550-8. doi: 10.1111/j.1530-0277.2010.01372.x. Epub 2010 Dec 8.
8
Improving detection of colorectal cancer.
Practitioner. 2010 Oct;254(1733):17-21, 2-3.
10
A genome-wide association study of alcohol dependence.
Proc Natl Acad Sci U S A. 2010 Mar 16;107(11):5082-7. doi: 10.1073/pnas.0911109107. Epub 2010 Mar 2.

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