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Alcohol and DNA Methylation: An Epigenome-Wide Association Study in Blood and Normal Breast Tissue.
Wilson, Lauren E; Xu, Zongli; Harlid, Sophia; White, Alexandra J; Troester, Melissa A; Sandler, Dale P; Taylor, Jack A.
Afiliação
  • Wilson LE; Epidemiology Branch, National Institute of Environmental Health Sciences, Research Triangle Park, North Carolina.
  • Xu Z; Department of Population Health Sciences, Duke University School of Medicine, Durham, North Carolina.
  • Harlid S; Epidemiology Branch, National Institute of Environmental Health Sciences, Research Triangle Park, North Carolina.
  • White AJ; Epidemiology Branch, National Institute of Environmental Health Sciences, Research Triangle Park, North Carolina.
  • Troester MA; Department of Radiation Sciences, Oncology, Umea University, Umea, Sweden.
  • Sandler DP; Epidemiology Branch, National Institute of Environmental Health Sciences, Research Triangle Park, North Carolina.
  • Taylor JA; Department of Epidemiology, Gillings School of Global Public Health, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina.
Am J Epidemiol ; 188(6): 1055-1065, 2019 06 01.
Article em En | MEDLINE | ID: mdl-30938765
ABSTRACT
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.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Consumo de Bebidas Alcoólicas / Ilhas de CpG / Metilação de DNA / Epigenoma Tipo de estudo: Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adult / Female / Humans / Middle aged País como assunto: America do norte Idioma: En Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Consumo de Bebidas Alcoólicas / Ilhas de CpG / Metilação de DNA / Epigenoma Tipo de estudo: Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adult / Female / Humans / Middle aged País como assunto: America do norte Idioma: En Ano de publicação: 2019 Tipo de documento: Article