Epidemiology Branch, National Institute of Environmental Health Sciences, Research Triangle Park, North Carolina.
Department of Population Health Sciences, Duke University School of Medicine, Durham, North Carolina.
Am J Epidemiol. 2019 Jun 1;188(6):1055-1065. doi: 10.1093/aje/kwz032.
The biological mechanisms driving associations between alcohol consumption and chronic diseases might include epigenetic modification of DNA methylation. We explored the hypothesis that alcohol consumption is associated with methylation in an epigenome-wide association study of blood and normal breast tissue DNA. Infinium HumanMethylation450 BeadChip (Illumina Inc., San Diego, California) array data on blood DNA methylation was examined in a discovery set of 2,878 non-Hispanic white women from the Sister Study (United States, 2004-2015) who provided detailed questionnaire information on lifetime alcohol use. Robust linear regression modeling was used to identify significant associations (false discovery rate of Q < 0.05) between the number of alcoholic drinks per week and DNA methylation at 5,458 cytosine-phosphate-guanine (CpG) sites. Associations were replicated (P < 0.05) for 677 CpGs in an independent set of 187 blood DNA samples from the Sister Study and for 628 CpGs in an independent set of 171 normal breast DNA samples; 1,207 CpGs were replicated in either blood or normal breast, with 98 CpGs replicated in both tissues. Individual gene effects were notable for phosphoglycerate dehydrogenase (PGHDH), peptidyl-prolyl cis-trans isomerase (PPIF), solute carrier 15 (SLC15), solute carrier family 43 member 1 (SLC43A1), and solute carrier family 7 member 11 (SLC7A11). We also found that high alcohol consumption was associated with significantly lower global methylation as measured by the average of CpGs on the entire array.
酒精摄入与慢性疾病之间关联的生物学机制可能包括 DNA 甲基化的表观遗传修饰。我们探索了这样一种假设,即酒精摄入与血液和正常乳腺组织 DNA 的全基因组关联研究中的甲基化有关。在一项对来自美国姐妹研究(2004-2015 年)的 2878 名非西班牙裔白人女性的血液 DNA 甲基化进行的发现组研究中,我们检查了基于 Infinium HumanMethylation450 BeadChip(Illumina Inc.,加利福尼亚州圣地亚哥)的全基因组关联研究阵列数据,这些女性提供了关于终生饮酒的详细问卷调查信息。使用稳健的线性回归模型来确定每周饮酒量与 5458 个胞嘧啶-磷酸-鸟嘌呤(CpG)位点的 DNA 甲基化之间的显著关联(错误发现率 Q < 0.05)。在姐妹研究的 187 个血液 DNA 样本的独立样本中,对 677 个 CpG 进行了复制(P < 0.05),在姐妹研究的 171 个正常乳腺 DNA 样本的独立样本中对 628 个 CpG 进行了复制;在血液或正常乳腺中复制了 1207 个 CpG,其中 98 个 CpG 在两个组织中均被复制。磷酸甘油酸脱氢酶(PGHDH)、肽基脯氨酰顺反异构酶(PPIF)、溶质载体 15(SLC15)、溶质载体家族 43 成员 1(SLC43A1)和溶质载体家族 7 成员 11(SLC7A11)的基因效应显著。我们还发现,高酒精摄入量与整个阵列上 CpG 的平均值表示的显著较低的全局甲基化有关。