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Race/ethnicity-associated blood DNA methylation differences between Japanese and European American women: an exploratory study
BACKGROUND: Racial/ethnic disparities in health reflect a combination of genetic and environmental causes, and DNA methylation may be an important mediator. We compared in an exploratory manner the blood DNA methylome of Japanese Americans (JPA) versus European Americans (EUA). METHODS: Genome-wide...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8507376/ https://www.ncbi.nlm.nih.gov/pubmed/34635168 http://dx.doi.org/10.1186/s13148-021-01171-w |
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author | Song, Min-Ae Seffernick, Anna Eames Archer, Kellie J. Mori, Kellie M. Park, Song-Yi Chang, Linda Ernst, Thomas Tiirikainen, Maarit Peplowska, Karolina Wilkens, Lynne R. Le Marchand, Loïc Lim, Unhee |
author_facet | Song, Min-Ae Seffernick, Anna Eames Archer, Kellie J. Mori, Kellie M. Park, Song-Yi Chang, Linda Ernst, Thomas Tiirikainen, Maarit Peplowska, Karolina Wilkens, Lynne R. Le Marchand, Loïc Lim, Unhee |
author_sort | Song, Min-Ae |
collection | PubMed |
description | BACKGROUND: Racial/ethnic disparities in health reflect a combination of genetic and environmental causes, and DNA methylation may be an important mediator. We compared in an exploratory manner the blood DNA methylome of Japanese Americans (JPA) versus European Americans (EUA). METHODS: Genome-wide buffy coat DNA methylation was profiled among healthy Multiethnic Cohort participant women who were Japanese (JPA; n = 30) or European (EUA; n = 28) Americans aged 60–65. Differentially methylated CpGs by race/ethnicity (DM-CpGs) were identified by linear regression (Bonferroni-corrected P < 0.1) and analyzed in relation to corresponding gene expression, a priori selected single nucleotide polymorphisms (SNPs), and blood biomarkers of inflammation and metabolism using Pearson or Spearman correlations (FDR < 0.1). RESULTS: We identified 174 DM-CpGs with the majority of hypermethylated in JPA compared to EUA (n = 133), often in promoter regions (n = 48). Half (51%) of the genes corresponding to the DM-CpGs were involved in liver function and liver disease, and the methylation in nine genes was significantly correlated with gene expression for DM-CpGs. A total of 156 DM-CpGs were associated with rs7489665 (SH2B1). Methylation of DM-CpGs was correlated with blood levels of the cytokine MIP1B (n = 146). We confirmed some of the DM-CpGs in the TCGA adjacent non-tumor liver tissue of Asians versus EUA. CONCLUSION: We found a number of differentially methylated CpGs in blood DNA between JPA and EUA women with a potential link to liver disease, specific SNPs, and systemic inflammation. These findings may support further research on the role of DNA methylation in mediating some of the higher risk of liver disease among JPA. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13148-021-01171-w. |
format | Online Article Text |
id | pubmed-8507376 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-85073762021-10-20 Race/ethnicity-associated blood DNA methylation differences between Japanese and European American women: an exploratory study Song, Min-Ae Seffernick, Anna Eames Archer, Kellie J. Mori, Kellie M. Park, Song-Yi Chang, Linda Ernst, Thomas Tiirikainen, Maarit Peplowska, Karolina Wilkens, Lynne R. Le Marchand, Loïc Lim, Unhee Clin Epigenetics Research BACKGROUND: Racial/ethnic disparities in health reflect a combination of genetic and environmental causes, and DNA methylation may be an important mediator. We compared in an exploratory manner the blood DNA methylome of Japanese Americans (JPA) versus European Americans (EUA). METHODS: Genome-wide buffy coat DNA methylation was profiled among healthy Multiethnic Cohort participant women who were Japanese (JPA; n = 30) or European (EUA; n = 28) Americans aged 60–65. Differentially methylated CpGs by race/ethnicity (DM-CpGs) were identified by linear regression (Bonferroni-corrected P < 0.1) and analyzed in relation to corresponding gene expression, a priori selected single nucleotide polymorphisms (SNPs), and blood biomarkers of inflammation and metabolism using Pearson or Spearman correlations (FDR < 0.1). RESULTS: We identified 174 DM-CpGs with the majority of hypermethylated in JPA compared to EUA (n = 133), often in promoter regions (n = 48). Half (51%) of the genes corresponding to the DM-CpGs were involved in liver function and liver disease, and the methylation in nine genes was significantly correlated with gene expression for DM-CpGs. A total of 156 DM-CpGs were associated with rs7489665 (SH2B1). Methylation of DM-CpGs was correlated with blood levels of the cytokine MIP1B (n = 146). We confirmed some of the DM-CpGs in the TCGA adjacent non-tumor liver tissue of Asians versus EUA. CONCLUSION: We found a number of differentially methylated CpGs in blood DNA between JPA and EUA women with a potential link to liver disease, specific SNPs, and systemic inflammation. These findings may support further research on the role of DNA methylation in mediating some of the higher risk of liver disease among JPA. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13148-021-01171-w. BioMed Central 2021-10-11 /pmc/articles/PMC8507376/ /pubmed/34635168 http://dx.doi.org/10.1186/s13148-021-01171-w Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Song, Min-Ae Seffernick, Anna Eames Archer, Kellie J. Mori, Kellie M. Park, Song-Yi Chang, Linda Ernst, Thomas Tiirikainen, Maarit Peplowska, Karolina Wilkens, Lynne R. Le Marchand, Loïc Lim, Unhee Race/ethnicity-associated blood DNA methylation differences between Japanese and European American women: an exploratory study |
title | Race/ethnicity-associated blood DNA methylation differences between Japanese and European American women: an exploratory study |
title_full | Race/ethnicity-associated blood DNA methylation differences between Japanese and European American women: an exploratory study |
title_fullStr | Race/ethnicity-associated blood DNA methylation differences between Japanese and European American women: an exploratory study |
title_full_unstemmed | Race/ethnicity-associated blood DNA methylation differences between Japanese and European American women: an exploratory study |
title_short | Race/ethnicity-associated blood DNA methylation differences between Japanese and European American women: an exploratory study |
title_sort | race/ethnicity-associated blood dna methylation differences between japanese and european american women: an exploratory study |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8507376/ https://www.ncbi.nlm.nih.gov/pubmed/34635168 http://dx.doi.org/10.1186/s13148-021-01171-w |
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