Department of Genetics, Texas Biomedical Research Institute, San Antonio, Texas.
Am J Med Genet B Neuropsychiatr Genet. 2014 Mar;165B(2):103-10. doi: 10.1002/ajmg.b.32213. Epub 2013 Nov 26.
Alcohol dependence (AD) is a moderately heritable phenotype with a small number of known risk genes mapped via linkage or candidate gene studies. We considered 313 males from among 595 members of documented, extended pedigrees in which AD segregates collected in Northern Hunan Province, China. A joint analysis of both males and females could not be performed as the difference in alcohol consumption variance was too large. Genome-wide association analyses were performed for approximately 300,000 single nucleotide polymorphisms (SNPs). Significant associations found in the ALDH2 region for AD (minimum P = 4.73 × 10(-8)) and two AD-related phenotypes: flushing response (minimum P = 4.75 × 10(-26)) and maximum drinks in a 24-hr period (minimum P = 1.54 × 10(-16)). Association of previous candidate SNP, rs10774610 in CCDC63, was confirmed but resulted from linkage disequilibrium with ALDH2. ALDH2 is strongly associated with flushing response, AD, and maximum drinks in males, with nonsynonymous SNP rs671 explaining 29.2%, 7.9%, and 22.9% of phenotypic variation, respectively, in this sample. When rs671 was considered as a candidate SNP in females, it explained 23.6% of the variation in flushing response, but alcohol consumption rates were too low among females-despite familial enrichment for AD-for an adequate test of association for either AD or maximum drinks. These results support a mediating effect of aldehyde dehydrogenase deficiency on alcohol consumption in males and a secondary, culturally mediated limitation on alcohol consumption by females that should be appropriately modeled in future studies of alcohol consumption in populations where this may be a factor.
酒精依赖(AD)是一种中度遗传表型,通过连锁或候选基因研究已经确定了少数已知的风险基因。我们考虑了来自中国湖南北部收集的有记录的扩展家系中的 595 名成员中的 313 名男性,这些家系中 AD 是可分离的。由于饮酒方差差异太大,无法对男性和女性进行联合分析。对大约 300,000 个单核苷酸多态性(SNP)进行了全基因组关联分析。在 AD(最小 P = 4.73×10(-8)) 和两个 AD 相关表型的 ALDH2 区域发现了显著关联:潮红反应(最小 P = 4.75×10(-26)) 和 24 小时内最大饮酒量(最小 P = 1.54×10(-16))。先前候选 SNP rs10774610 在 CCDC63 中的关联得到了证实,但由于与 ALDH2 的连锁不平衡而导致。ALDH2 与潮红反应、AD 和男性最大饮酒量强烈相关,非同义 SNP rs671 分别解释了该样本中表型变异的 29.2%、7.9%和 22.9%。当 rs671 被视为女性中的候选 SNP 时,它解释了潮红反应变异的 23.6%,但女性的饮酒率太低-尽管 AD 的家族聚集率很高-对于 AD 或最大饮酒量的关联测试都不够充分。这些结果支持乙醛脱氢酶缺乏症对男性饮酒量的中介作用,以及女性饮酒量的次要、文化介导的限制,在未来的人群饮酒研究中应该适当考虑到这一因素。