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拷贝数变异对韩国人群酒精中毒风险的遗传效应。

The genetic effect of copy number variations on the risk of alcoholism in a Korean population.

机构信息

Department of Life Science, Laboratory of Genomic Diversity, Sogang University, Shinsu-dong, Mapo-gu, Seoul, Korea.

出版信息

Alcohol Clin Exp Res. 2012 Jan;36(1):35-42. doi: 10.1111/j.1530-0277.2011.01578.x. Epub 2011 Jul 25.

Abstract

BACKGROUND

Alcoholism, a chronic behavioral disorder characterized by excessive alcohol consumption, has been a leading cause of morbidity and premature death. This condition is believed to be influenced by genetic factors. As copy number variation (CNV) has been recently discovered in human genome, genomic diversity of human genome is more frequent than previously thought. Many studies have reported evidences that CNV is associated with the development of complex diseases. In this study, we hypothesized that CNV can predict the risk of alcoholism.

METHODS

Using the Illumina HumanHap660W-Quad BeadChip (∼660 k markers), genome-wide genotyping was performed to obtain signal and allelic intensities from 116 alcoholic cases and 1,022 healthy controls (total n = 1,138) in a Korean population. To identify alcoholism-associated CNV regions, we performed a genome-wide association analysis, using multivariate logistic regression model controlling for age and gender.

RESULTS

We identified a total of 255,732 individual CNVs and 3,261 CNV regions (1,067 common CNV regions, frequency > 1%) in this study. Results from multivariate logistic regression showed that the chr20:61195302-61195978 regions were significantly associated with the risk of alcoholism after multiple corrections (p = 5.02E-05, p(corr) = 0.04). Most of the identified variations in this study overlapped with the previously reported CNVs in the Database of Genomic Variants (95.3%). The identified CNVs, which encompassed 3,226 functional genes, were significantly enriched in the cellular part, in the membrane-bound organelle, in the cell part, in developmental processes, in cell communication, in neurological system process, in sensory perception of smell and chemical stimulus, and in olfactory receptor activity.

CONCLUSIONS

This is the first genome-wide association study to investigate the relationship between common CNV and alcoholism. Our results suggest that the newly identified CNV regions may contribute to the development of alcoholism.

摘要

背景

酒精中毒是一种以过度饮酒为特征的慢性行为障碍,是发病率和早逝的主要原因。这种情况被认为受遗传因素的影响。由于人类基因组中最近发现了拷贝数变异(CNV),人类基因组的基因组多样性比以前想象的更为频繁。许多研究报告表明,CNV 与复杂疾病的发展有关。在这项研究中,我们假设 CNV 可以预测酒精中毒的风险。

方法

使用 Illumina HumanHap660W-Quad BeadChip(约 660k 个标记),对来自韩国人群的 116 例酒精中毒病例和 1022 例健康对照者(共 1138 例)进行全基因组基因分型,以获得信号和等位基因强度。为了鉴定与酒精中毒相关的 CNV 区域,我们使用多元逻辑回归模型进行了全基因组关联分析,该模型控制了年龄和性别。

结果

在这项研究中,我们总共鉴定出 255732 个个体 CNV 和 3261 个 CNV 区域(1067 个常见 CNV 区域,频率>1%)。多元逻辑回归分析结果显示,chr20:61195302-61195978 区域在经过多次校正后与酒精中毒的风险显著相关(p=5.02E-05,p(corr)=0.04)。本研究中大多数鉴定出的变异与数据库中的先前报道的 CNV 重叠基因组变异(95.3%)。所鉴定的 CNV 包含 3226 个功能基因,在细胞部分、膜结合细胞器、细胞部分、发育过程、细胞通讯、神经系统过程、嗅觉和化学刺激的感觉感知以及嗅觉受体活性中显著富集。

结论

这是首次进行全基因组关联研究,以调查常见 CNV 与酒精中毒之间的关系。我们的研究结果表明,新鉴定的 CNV 区域可能有助于酒精中毒的发展。

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