Office of Biostatistics Research, National Heart, Lung, and Blood Institute, NIH, 6701 Rockledge Drive, MSC 7938, Bethesda, MD 20892-7938, USA.
BMC Genet. 2005 Dec 30;6 Suppl 1(Suppl 1):S114. doi: 10.1186/1471-2156-6-S1-S114.
Genetic components significantly contribute to the susceptibilities of alcoholism and its endophenotypes, such as event-related potential measures and electroencephalogram. An endophenotype is a correlated trait which identifies individuals at risk. Correlated traits could be influenced by shared genes. This study is intended to identify chromosome regions that may harbor common genetic loci contributing to alcoholism, event related potential measures and electroencephalogram. All 143 Collaborative Study on the Genetics of Alcoholism families with 1,614 individuals provided by the Genetic Analysis Workshop 14 were used for the analysis with aldx1 as an alcoholism diagnosis. We carried out factor and principal component analyses on the 12 event-related potentials, then bivariate genome scans on aldx1 and electroencephalogram (ecb21), as well as alcoholism and the principal component scores of the event-related potential measures. A univariate genome scan was also carried out on each trait. Factor and principal component analysis on the event-related potential measures showed that the 4 ttths and 4 ntths belong to one cluster (cluster 1), while the 4 ttdts belonged to another (cluster 2). From each cluster, one principal component was extracted and saved as pc1 (for cluster 1) and pc2 (for cluster 2). The results of genome scans revealed only one chromosome region, chromosome 4 q at about 100 cM, identified by several univariate genome scans including aldx1, ecb21, and pc2, and the evidence of linkage increased significantly in the bivariate genome scans of aldx1 and ecb21 and aldx1 and pc2. Our study suggests that the same quantitative trait locus on the chromosome 4 q region, where ADH3 is located, may influence the risk of alcoholism, variations of electroencephalogram, and the 4 ttdts of the event-related potential measures.
遗传因素对酗酒及其表型(如事件相关电位和脑电图)的易感性有重要贡献。表型是一种相关特征,可以识别处于风险中的个体。相关特征可能受共同基因的影响。本研究旨在确定可能包含导致酗酒、事件相关电位和脑电图的共同遗传位点的染色体区域。遗传分析研讨会 14 提供的 143 个协作性酒精遗传研究家族的 1614 名个体全部用于分析,其中 aldx1 作为酒精诊断。我们对 12 个事件相关电位进行了因子和主成分分析,然后对 aldx1 和脑电图(ecb21)以及酗酒和事件相关电位测量的主成分得分进行了双变量基因组扫描。还对每个特征进行了单变量基因组扫描。对事件相关电位测量的因子和主成分分析表明,4 个 ttths 和 4 个 ntths 属于一个簇(簇 1),而 4 个 ttdts 属于另一个簇(簇 2)。从每个簇中提取一个主成分并保存为 pc1(用于簇 1)和 pc2(用于簇 2)。基因组扫描的结果仅显示一个染色体区域,即染色体 4q 约 100cM,被包括 aldx1、ecb21 和 pc2 在内的几个单变量基因组扫描识别,并且在 aldx1 和 ecb21 以及 aldx1 和 pc2 的双变量基因组扫描中,连锁的证据显著增加。我们的研究表明,染色体 4q 区域上的相同数量性状基因座,即 ADH3 所在的位置,可能会影响酗酒、脑电图变化以及事件相关电位的 4 个 ttdts 的风险。