Cargando…
Bisphenol A-associated epigenomic changes in prepubescent girls: a cross-sectional study in Gharbiah, Egypt
BACKGROUND: There is now compelling evidence that epigenetic modifications link adult disease susceptibility to environmental exposures during specific life stages, including pre-pubertal development. Animal studies indicate that bisphenol A (BPA), the monomer used in epoxy resins and polycarbonate...
Autores principales: | , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2013
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3655072/ https://www.ncbi.nlm.nih.gov/pubmed/23590724 http://dx.doi.org/10.1186/1476-069X-12-33 |
_version_ | 1782269827082092544 |
---|---|
author | Kim, Jung H Rozek, Laura S Soliman, Amr S Sartor, Maureen A Hablas, Ahmed Seifeldin, Ibrahim A Colacino, Justin A Weinhouse, Caren Nahar, Muna S Dolinoy, Dana C |
author_facet | Kim, Jung H Rozek, Laura S Soliman, Amr S Sartor, Maureen A Hablas, Ahmed Seifeldin, Ibrahim A Colacino, Justin A Weinhouse, Caren Nahar, Muna S Dolinoy, Dana C |
author_sort | Kim, Jung H |
collection | PubMed |
description | BACKGROUND: There is now compelling evidence that epigenetic modifications link adult disease susceptibility to environmental exposures during specific life stages, including pre-pubertal development. Animal studies indicate that bisphenol A (BPA), the monomer used in epoxy resins and polycarbonate plastics, may impact health through epigenetic mechanisms, and epidemiological data associate BPA levels with metabolic disorders, behavior changes, and reproductive effects. Thus, we conducted an environmental epidemiology study of BPA exposure and CpG methylation in pre-adolescent girls from Gharbiah, Egypt hypothesizing that methylation profiles exhibit exposure-dependent trends. METHODS: Urinary concentrations of total (free plus conjugated) species of BPA in spot samples were quantified for 60 girls aged 10 to 13. Genome-wide CpG methylation was concurrently measured in bisulfite-converted saliva DNA using the Infinium HumanMethylation27 BeadChip (N = 46). CpG sites from four candidate genes were validated via quantitative bisulfite pyrosequencing. RESULTS: CpG methylation varied widely among girls, and higher urinary BPA concentrations were generally associated with less genomic methylation. Based on pathway analyses, genes exhibiting reduced methylation with increasing urinary BPA were involved in immune function, transport activity, metabolism, and caspase activity. In particular, hypomethylation of CpG targets on chromosome X was associated with higher urinary BPA. Using the Comparative Toxicogenomics Database, we identified a number of candidate genes in our sample that previously have been associated with BPA-related expression change. CONCLUSIONS: These data indicate that BPA may affect human health through specific epigenomic modification of genes in relevant pathways. Thus, epigenetic epidemiology holds promise for the identification of biomarkers from previous exposures and the development of epigenetic-based diagnostic strategies. |
format | Online Article Text |
id | pubmed-3655072 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-36550722013-05-20 Bisphenol A-associated epigenomic changes in prepubescent girls: a cross-sectional study in Gharbiah, Egypt Kim, Jung H Rozek, Laura S Soliman, Amr S Sartor, Maureen A Hablas, Ahmed Seifeldin, Ibrahim A Colacino, Justin A Weinhouse, Caren Nahar, Muna S Dolinoy, Dana C Environ Health Research BACKGROUND: There is now compelling evidence that epigenetic modifications link adult disease susceptibility to environmental exposures during specific life stages, including pre-pubertal development. Animal studies indicate that bisphenol A (BPA), the monomer used in epoxy resins and polycarbonate plastics, may impact health through epigenetic mechanisms, and epidemiological data associate BPA levels with metabolic disorders, behavior changes, and reproductive effects. Thus, we conducted an environmental epidemiology study of BPA exposure and CpG methylation in pre-adolescent girls from Gharbiah, Egypt hypothesizing that methylation profiles exhibit exposure-dependent trends. METHODS: Urinary concentrations of total (free plus conjugated) species of BPA in spot samples were quantified for 60 girls aged 10 to 13. Genome-wide CpG methylation was concurrently measured in bisulfite-converted saliva DNA using the Infinium HumanMethylation27 BeadChip (N = 46). CpG sites from four candidate genes were validated via quantitative bisulfite pyrosequencing. RESULTS: CpG methylation varied widely among girls, and higher urinary BPA concentrations were generally associated with less genomic methylation. Based on pathway analyses, genes exhibiting reduced methylation with increasing urinary BPA were involved in immune function, transport activity, metabolism, and caspase activity. In particular, hypomethylation of CpG targets on chromosome X was associated with higher urinary BPA. Using the Comparative Toxicogenomics Database, we identified a number of candidate genes in our sample that previously have been associated with BPA-related expression change. CONCLUSIONS: These data indicate that BPA may affect human health through specific epigenomic modification of genes in relevant pathways. Thus, epigenetic epidemiology holds promise for the identification of biomarkers from previous exposures and the development of epigenetic-based diagnostic strategies. BioMed Central 2013-04-16 /pmc/articles/PMC3655072/ /pubmed/23590724 http://dx.doi.org/10.1186/1476-069X-12-33 Text en Copyright © 2013 Kim et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Kim, Jung H Rozek, Laura S Soliman, Amr S Sartor, Maureen A Hablas, Ahmed Seifeldin, Ibrahim A Colacino, Justin A Weinhouse, Caren Nahar, Muna S Dolinoy, Dana C Bisphenol A-associated epigenomic changes in prepubescent girls: a cross-sectional study in Gharbiah, Egypt |
title | Bisphenol A-associated epigenomic changes in prepubescent girls: a cross-sectional study in Gharbiah, Egypt |
title_full | Bisphenol A-associated epigenomic changes in prepubescent girls: a cross-sectional study in Gharbiah, Egypt |
title_fullStr | Bisphenol A-associated epigenomic changes in prepubescent girls: a cross-sectional study in Gharbiah, Egypt |
title_full_unstemmed | Bisphenol A-associated epigenomic changes in prepubescent girls: a cross-sectional study in Gharbiah, Egypt |
title_short | Bisphenol A-associated epigenomic changes in prepubescent girls: a cross-sectional study in Gharbiah, Egypt |
title_sort | bisphenol a-associated epigenomic changes in prepubescent girls: a cross-sectional study in gharbiah, egypt |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3655072/ https://www.ncbi.nlm.nih.gov/pubmed/23590724 http://dx.doi.org/10.1186/1476-069X-12-33 |
work_keys_str_mv | AT kimjungh bisphenolaassociatedepigenomicchangesinprepubescentgirlsacrosssectionalstudyingharbiahegypt AT rozeklauras bisphenolaassociatedepigenomicchangesinprepubescentgirlsacrosssectionalstudyingharbiahegypt AT solimanamrs bisphenolaassociatedepigenomicchangesinprepubescentgirlsacrosssectionalstudyingharbiahegypt AT sartormaureena bisphenolaassociatedepigenomicchangesinprepubescentgirlsacrosssectionalstudyingharbiahegypt AT hablasahmed bisphenolaassociatedepigenomicchangesinprepubescentgirlsacrosssectionalstudyingharbiahegypt AT seifeldinibrahima bisphenolaassociatedepigenomicchangesinprepubescentgirlsacrosssectionalstudyingharbiahegypt AT colacinojustina bisphenolaassociatedepigenomicchangesinprepubescentgirlsacrosssectionalstudyingharbiahegypt AT weinhousecaren bisphenolaassociatedepigenomicchangesinprepubescentgirlsacrosssectionalstudyingharbiahegypt AT naharmunas bisphenolaassociatedepigenomicchangesinprepubescentgirlsacrosssectionalstudyingharbiahegypt AT dolinoydanac bisphenolaassociatedepigenomicchangesinprepubescentgirlsacrosssectionalstudyingharbiahegypt |