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The Collaborative Study on the Genetics of Alcoholism.酒精中毒遗传学合作研究
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Genome-wide association study of alcohol dependence implicates a region on chromosome 11.全基因组关联研究提示染色体 11 上的一个区域与酒精依赖有关。
Alcohol Clin Exp Res. 2010 May;34(5):840-52. doi: 10.1111/j.1530-0277.2010.01156.x. Epub 2010 Mar 1.
3
Role of GABRA2 in trajectories of externalizing behavior across development and evidence of moderation by parental monitoring.GABRA2在整个发育过程中外部行为轨迹中的作用以及父母监督调节作用的证据。
Arch Gen Psychiatry. 2009 Jun;66(6):649-57. doi: 10.1001/archgenpsychiatry.2009.48.
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A test of the reactive aggression-suicidal behavior hypothesis: is there a case for proactive aggression?反应性攻击-自杀行为假说的一项检验:主动攻击是否有依据?
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Gene-wide analyses of genome-wide association data sets: evidence for multiple common risk alleles for schizophrenia and bipolar disorder and for overlap in genetic risk.全基因组关联数据集的基因层面分析:精神分裂症和双相情感障碍存在多个常见风险等位基因及遗传风险重叠的证据。
Mol Psychiatry. 2009 Mar;14(3):252-60. doi: 10.1038/mp.2008.133. Epub 2008 Dec 9.
6
Neuropeptide Y receptor genes are associated with alcohol dependence, alcohol withdrawal phenotypes, and cocaine dependence.神经肽Y受体基因与酒精依赖、酒精戒断表型及可卡因依赖相关。
Alcohol Clin Exp Res. 2008 Dec;32(12):2031-40. doi: 10.1111/j.1530-0277.2008.00790.x. Epub 2008 Sep 25.
7
The role of GABA(A) receptors in the development of alcoholism.γ-氨基丁酸A型(GABA(A))受体在酒精中毒发展过程中的作用。
Pharmacol Biochem Behav. 2008 Jul;90(1):95-104. doi: 10.1016/j.pbb.2008.03.007. Epub 2008 Mar 15.
8
A Systematic single nucleotide polymorphism screen to fine-map alcohol dependence genes on chromosome 7 identifies association with a novel susceptibility gene ACN9.一项用于在7号染色体上精细定位酒精依赖基因的系统性单核苷酸多态性筛查,确定了与一个新的易感基因ACN9的关联。
Biol Psychiatry. 2008 Jun 1;63(11):1047-53. doi: 10.1016/j.biopsych.2007.11.005. Epub 2007 Dec 27.
9
Association of NFKB1, which encodes a subunit of the transcription factor NF-kappaB, with alcohol dependence.编码转录因子NF-κB一个亚基的NFKB1与酒精依赖的关联。
Hum Mol Genet. 2008 Apr 1;17(7):963-70. doi: 10.1093/hmg/ddm368. Epub 2007 Dec 12.
10
Linkage scan for quantitative traits identifies new regions of interest for substance dependence in the Collaborative Study on the Genetics of Alcoholism (COGA) sample.酒精中毒遗传学合作研究(COGA)样本中对数量性状的连锁扫描确定了物质依赖新的感兴趣区域。
Drug Alcohol Depend. 2008 Jan 11;93(1-2):12-20. doi: 10.1016/j.drugalcdep.2007.08.015. Epub 2007 Oct 17.

有证据表明,2 号染色体上的基因与伴有品行障碍和自杀未遂的酒精依赖有关。

Evidence for genes on chromosome 2 contributing to alcohol dependence with conduct disorder and suicide attempts.

机构信息

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

出版信息

Am J Med Genet B Neuropsychiatr Genet. 2010 Sep;153B(6):1179-88. doi: 10.1002/ajmg.b.31089.

DOI:10.1002/ajmg.b.31089
PMID:20468071
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3597340/
Abstract

Twin studies provide strong evidence that there is a shared genetic liability that predisposes to a number of different psychiatric outcomes related to behavioral disinhibition. Further, alcohol dependence comorbid with other disinhibitory disorders is particularly heritable. Chromosome 2p14-2q14.3 has been linked to multiple psychiatric conditions related to behavioral undercontrol. In the Collaborative Study on the Genetics of Alcoholism (COGA), we previously reported linkage to this region with alcohol dependence (AD), suicide attempts (SUI), and conduct disorder (CD). In this study, we follow-up on these previous reports of linkage by combining the phenotypes in analyses that jointly consider the presence of multiple conditions. Linkage analyses of the combined phenotype of AD with CD or SUI results in a maximum LOD score of 5.4 in this region. In addition to this primary linkage peak, independent samples have reported linkage to other alcohol-related phenotypes across chromosome 2. Accordingly, we followed-up these linkage signals by testing for association with SNPs across chromosome 2 in a case-control sample, in which a subset of the cases consisted of alcohol-dependent probands from the linkage sample. We find evidence of association with the combined AD with CD or SUI phenotype, with 23 genes surviving permutation testing. The number of associated genes across the chromosome may explain the persistent linkage findings reported on chromosome 2 across a number of independent studies of alcohol and disinhibitory phenotypes. Further, none of the genes were located directly under the primary COGA linkage peak, which has implications for association tests following-up linkage peaks.

摘要

双生子研究提供了有力的证据表明,存在着一种共同的遗传易感性,使个体易患多种与行为抑制障碍相关的不同精神疾病。此外,与其他抑制障碍共病的酒精依赖具有很强的遗传性。染色体 2p14-2q14.3 与多种与行为失控相关的精神疾病有关。在酒精依赖的遗传学合作研究(COGA)中,我们先前报道了该区域与酒精依赖(AD)、自杀未遂(SUI)和品行障碍(CD)的连锁。在这项研究中,我们通过联合分析共同考虑多种疾病的存在,对先前的连锁报告进行了跟进。联合分析 AD 与 CD 或 SUI 的表型,该区域的最大 LOD 评分为 5.4。除了这个主要的连锁峰之外,独立样本报告了在染色体 2 上与其他与酒精相关的表型的连锁。因此,我们在一个病例对照样本中,通过测试横跨染色体 2 的 SNP 与这些连锁信号进行了关联分析,其中一个亚组病例由连锁样本中的酒精依赖先证者组成。我们发现了与 AD 与 CD 或 SUI 表型联合的关联证据,有 23 个基因在置换检验中幸存。在许多独立的酒精和抑制障碍表型研究中,该染色体上的关联基因数量可能解释了染色体 2 上持续存在的连锁发现。此外,没有一个基因直接位于 COGA 连锁峰的主要区域之下,这对连锁峰的关联测试有影响。