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Alcohol and nicotine codependence-associated DNA methylation changes in promoter regions of addiction-related genes
Altered DNA methylation in addiction-related genes may modify the susceptibility to alcohol or drug dependence (AD or ND). We profiled peripheral blood DNA methylation levels of 384 CpGs in promoter regions of 82 addiction-related genes in 256 African Americans (AAs) (117 cases with AD-ND codependen...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5292964/ https://www.ncbi.nlm.nih.gov/pubmed/28165486 http://dx.doi.org/10.1038/srep41816 |
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author | Xu, Hongqin Wang, Fan Kranzler, Henry R. Gelernter, Joel Zhang, Huiping |
author_facet | Xu, Hongqin Wang, Fan Kranzler, Henry R. Gelernter, Joel Zhang, Huiping |
author_sort | Xu, Hongqin |
collection | PubMed |
description | Altered DNA methylation in addiction-related genes may modify the susceptibility to alcohol or drug dependence (AD or ND). We profiled peripheral blood DNA methylation levels of 384 CpGs in promoter regions of 82 addiction-related genes in 256 African Americans (AAs) (117 cases with AD-ND codependence and 139 controls) and 196 European Americans (103 cases with AD-ND codependence and 93 controls) using Illumina’s GoldenGate DNA methylation array assays. AD-ND codependence-associated DNA methylation changes were analyzed using linear mixed-effects models with consideration of batch effects and covariates age, sex, and ancestry proportions. Seventy CpGs (in 41 genes) showed nominally significant associations (P < 0.05) with AD-ND codependence in both AAs and EAs. One CpG (HTR2B cg27531267) was hypomethylated in AA cases (P = 7.2 × 10(−5)), while 17 CpGs in 16 genes (including HTR2B cg27531267) were hypermethylated in EA cases (5.6 × 10(−9) ≤ P ≤ 9.5 × 10(−5)). Nevertheless, 13 single nucleotide polymorphisms (SNPs) nearby HTR2B cg27531267 and the interaction of these SNPs and cg27531267 did not show significant effects on AD-ND codependence in either AAs or EAs. Our study demonstrated that DNA methylation changes in addiction-related genes could be potential biomarkers for AD-ND co-dependence. Future studies need to explore whether DNA methylation alterations influence the risk of AD-ND codependence or the other way around. |
format | Online Article Text |
id | pubmed-5292964 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-52929642017-02-10 Alcohol and nicotine codependence-associated DNA methylation changes in promoter regions of addiction-related genes Xu, Hongqin Wang, Fan Kranzler, Henry R. Gelernter, Joel Zhang, Huiping Sci Rep Article Altered DNA methylation in addiction-related genes may modify the susceptibility to alcohol or drug dependence (AD or ND). We profiled peripheral blood DNA methylation levels of 384 CpGs in promoter regions of 82 addiction-related genes in 256 African Americans (AAs) (117 cases with AD-ND codependence and 139 controls) and 196 European Americans (103 cases with AD-ND codependence and 93 controls) using Illumina’s GoldenGate DNA methylation array assays. AD-ND codependence-associated DNA methylation changes were analyzed using linear mixed-effects models with consideration of batch effects and covariates age, sex, and ancestry proportions. Seventy CpGs (in 41 genes) showed nominally significant associations (P < 0.05) with AD-ND codependence in both AAs and EAs. One CpG (HTR2B cg27531267) was hypomethylated in AA cases (P = 7.2 × 10(−5)), while 17 CpGs in 16 genes (including HTR2B cg27531267) were hypermethylated in EA cases (5.6 × 10(−9) ≤ P ≤ 9.5 × 10(−5)). Nevertheless, 13 single nucleotide polymorphisms (SNPs) nearby HTR2B cg27531267 and the interaction of these SNPs and cg27531267 did not show significant effects on AD-ND codependence in either AAs or EAs. Our study demonstrated that DNA methylation changes in addiction-related genes could be potential biomarkers for AD-ND co-dependence. Future studies need to explore whether DNA methylation alterations influence the risk of AD-ND codependence or the other way around. Nature Publishing Group 2017-02-06 /pmc/articles/PMC5292964/ /pubmed/28165486 http://dx.doi.org/10.1038/srep41816 Text en Copyright © 2017, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Xu, Hongqin Wang, Fan Kranzler, Henry R. Gelernter, Joel Zhang, Huiping Alcohol and nicotine codependence-associated DNA methylation changes in promoter regions of addiction-related genes |
title | Alcohol and nicotine codependence-associated DNA methylation changes in promoter regions of addiction-related genes |
title_full | Alcohol and nicotine codependence-associated DNA methylation changes in promoter regions of addiction-related genes |
title_fullStr | Alcohol and nicotine codependence-associated DNA methylation changes in promoter regions of addiction-related genes |
title_full_unstemmed | Alcohol and nicotine codependence-associated DNA methylation changes in promoter regions of addiction-related genes |
title_short | Alcohol and nicotine codependence-associated DNA methylation changes in promoter regions of addiction-related genes |
title_sort | alcohol and nicotine codependence-associated dna methylation changes in promoter regions of addiction-related genes |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5292964/ https://www.ncbi.nlm.nih.gov/pubmed/28165486 http://dx.doi.org/10.1038/srep41816 |
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