Department of Psychiatry, Virginia Institute for Psychiatric and Behavioral Genetics, Virginia Commonwealth University, Richmond, VA 23298-0126, USA.
Am J Med Genet B Neuropsychiatr Genet. 2010 Sep;153B(6):1179-88. doi: 10.1002/ajmg.b.31089.
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.
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。