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OpenMx: An Open Source Extended Structural Equation Modeling Framework.OpenMx:一个开源的扩展结构方程建模框架。
Psychometrika. 2011 Apr 1;76(2):306-317. doi: 10.1007/s11336-010-9200-6.
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Genetic influences on craving for alcohol.酒精渴求的遗传影响。
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Clinical approaches to improving alcohol education and counseling in adolescents and young adults.改善青少年和青年酒精教育与咨询的临床方法。
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A novel, functional and replicable risk gene region for alcohol dependence identified by genome-wide association study.通过全基因组关联研究鉴定到一个新颖的、功能性的、可复制的与酒精依赖相关的风险基因区域。
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Genome-wide association study identifies 5q21 and 9p24.1 (KDM4C) loci associated with alcohol withdrawal symptoms.全基因组关联研究鉴定出与酒精戒断症状相关的 5q21 和 9p24.1(KDM4C)位点。
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Economic costs of excessive alcohol consumption in the U.S., 2006.美国 2006 年过度饮酒的经济成本。
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Genome-wide significant association between alcohol dependence and a variant in the ADH gene cluster.全基因组范围内发现与酒精依赖相关的 ADH 基因簇变异与酒精依赖存在显著关联。
Addict Biol. 2012 Jan;17(1):171-80. doi: 10.1111/j.1369-1600.2011.00395.x. Epub 2011 Oct 18.
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Alcohol and wine in relation to cancer and other diseases.酒精与癌症和其他疾病的关系。
Eur J Cancer Prev. 2012 Jan;21(1):103-8. doi: 10.1097/CEJ.0b013e32834761d3.
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Genome-wide association study of alcohol dependence implicates KIAA0040 on chromosome 1q.全基因组关联研究提示染色体 1q 上的 KIAA0040 与酒精依赖有关。
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Trends in adolescent alcohol use: effects of age, sex and cohort on prevalence and heritability.青少年饮酒趋势:年龄、性别和队列对流行率和遗传性的影响。
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男性的饮酒行为受到青春期和成年期不同性质的遗传因素的影响。

Alcohol consumption in men is influenced by qualitatively different genetic factors in adolescence and adulthood.

机构信息

Virginia Institute for Psychiatric and Behavioral Genetics, Department of Psychiatry, Virginia Commonwealth University, Richmond, VA 23298-0126, USA.

出版信息

Psychol Med. 2013 Sep;43(9):1857-68. doi: 10.1017/S0033291712002917. Epub 2013 Jan 2.

DOI:10.1017/S0033291712002917
PMID:23282961
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3670965/
Abstract

BACKGROUND

Alcohol consumption is influenced by genetic factors. Previous studies have examined the heritability of alcohol consumption, or related phenotypes, from adolescence into adulthood, frequently finding that total heritability changes over time. However, it remains unclear whether the same genes underlie liability to alcohol consumption across development versus whether novel risk genes become important over time. Method A population-based study of adult male twins (n=1790) born in Virginia, USA, retrospectively reported on their average monthly alcohol consumption from early adolescence through adulthood. We used twin modeling methods to explore genetic and environmental influences on alcohol consumption over time.

RESULTS

One latent genetic factor accounted for the majority of the heritability in alcohol consumption during mid- to late adolescence, but its influence declined thereafter; from young adulthood forward, heritability was largely attributable to a second genetic factor. The total heritability of alcohol consumption increased from 0 at ages 12-14 years to 0.40 by ages 18-21 years. Shared environmental factors declined in influence over time.

CONCLUSIONS

The heritability of alcohol consumption over time is dynamic both quantitatively and qualitatively. These results have important implications for gene identification endeavors. Furthermore, these findings could inform efforts to elucidate developmentally dynamic behaviors, such as antisocial behavior.

摘要

背景

饮酒行为受到遗传因素的影响。先前的研究已经考察了从青春期到成年期饮酒量或相关表型的遗传性,经常发现总遗传性随时间而变化。然而,目前尚不清楚在发展过程中是否存在导致饮酒倾向的相同基因,或者是否随着时间的推移会出现新的风险基因。方法:一项基于人群的美国弗吉尼亚州成年男性双胞胎研究(n=1790),回顾性地报告了他们从青少年早期到成年期的平均每月饮酒量。我们使用双胞胎建模方法来探讨随时间推移饮酒量的遗传和环境影响。

结果

一个潜在的遗传因素解释了青少年中期到后期饮酒量的大部分遗传性,但此后其影响下降;从青年期开始,遗传性主要归因于第二个遗传因素。饮酒量的总遗传性从 12-14 岁时的 0 增加到 18-21 岁时的 0.40。共享环境因素的影响随时间下降。

结论

饮酒量随时间的遗传性在数量和质量上都是动态的。这些结果对基因识别工作具有重要意义。此外,这些发现可以为阐明发展动态行为(如反社会行为)的努力提供信息。