Department of Psychology, Virginia Commonwealth University, Richmond, Virginia.
Virginia Institute for Psychiatric and Behavioral Genetics, Virginia Commonwealth University, Richmond, Virginia.
Alcohol Clin Exp Res. 2018 Feb;42(2):413-423. doi: 10.1111/acer.13551. Epub 2017 Dec 19.
Characterizing aggregate genetic risk for alcohol misuse and identifying variants involved in gene-by-environment (G × E) interaction effects has so far been a major challenge. We hypothesized that functional genomic information could be used to enhance detection of polygenic signal underlying alcohol misuse and to prioritize identification of single nucleotide polymorphisms (SNPs) most likely to exhibit G × E effects.
We examined these questions in the young adult FinnTwin12 sample (n = 1,170). We used genomewide association estimates from an independent sample to derive 2 types of polygenic scores for alcohol problems in FinnTwin12. Genomewide polygenic scores included all SNPs surpassing a designated p-value threshold. DNase polygenic scores were a subset of the genomewide polygenic scores including only variants in DNase I hypersensitive sites (DHSs), which are open chromatin marks likely to index regions with a regulatory function. We conducted parallel analyses using height as a nonpsychiatric model phenotype to evaluate the consistency of effects. For the G × E analyses, we examined whether SNPs in DHSs were overrepresented among SNPs demonstrating significant G × E effects in an interaction between romantic relationship status and intoxication frequency.
Contrary to our expectations, we found that DNase polygenic scores were not more strongly predictive of alcohol problems than conventional polygenic scores. However, variants in DNase polygenic scores had per-SNP effects that were up to 1.4 times larger than variants in conventional polygenic scores. This same pattern of effects was also observed in supplementary analyses with height. In G × E models, SNPs in DHSs were modestly overrepresented among SNPs with significant interaction effects for intoxication frequency.
These findings highlight the potential utility of integrating functional genomic annotation information to increase the signal-to-noise ratio in polygenic scores and identify genetic variants that may be most susceptible to environmental modification.
迄今为止,描述酒精滥用的综合遗传风险并确定参与基因-环境(G×E)相互作用效应的变异体一直是一个主要挑战。我们假设可以利用功能基因组信息来增强对酒精滥用潜在多基因信号的检测,并优先确定最有可能表现出 G×E 效应的单核苷酸多态性(SNP)。
我们在年轻的 FinnTwin12 样本(n=1170)中检验了这些问题。我们使用来自独立样本的全基因组关联估计值,为 FinnTwin12 中的酒精问题得出了 2 种多基因评分。全基因组多基因评分包括超过指定 p 值阈值的所有 SNP。DNase 多基因评分是全基因组多基因评分的一个子集,仅包括 DNase I 超敏位点(DHSs)中的变体,DHSs 是开放染色质标记,可能表示具有调节功能的区域。我们使用身高作为非精神疾病模型表型进行了平行分析,以评估效应的一致性。对于 G×E 分析,我们检查了 DHS 中的 SNP 是否在与浪漫关系状态和醉酒频率之间的相互作用中表现出显著 G×E 效应的 SNP 中过度表现。
与我们的预期相反,我们发现 DNase 多基因评分并不能比传统多基因评分更能预测酒精问题。然而,DNase 多基因评分中的变体的 SNP 效应高达传统多基因评分中变体的 1.4 倍。在使用身高的补充分析中也观察到了相同的效应模式。在 G×E 模型中,在 DHS 中的 SNP 中,在与醉酒频率有显著交互作用的 SNP 中适度过度表现。
这些发现强调了整合功能基因组注释信息的潜在效用,可以提高多基因评分中的信号与噪声比,并确定最容易受到环境修饰影响的遗传变异体。