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Associations of sex hormone-binding globulin and testosterone with genome-wide DNA methylation
BACKGROUND: Levels of sex hormone-binding globulin (SHBG) and the androgen testosterone have been associated with risk of diseases throughout the lifecourse. Although both SHBG and testosterone have been shown to be highly heritable, only a fraction of that heritability has been explained by genetic...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6295101/ https://www.ncbi.nlm.nih.gov/pubmed/30547757 http://dx.doi.org/10.1186/s12863-018-0703-y |
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author | Arathimos, Ryan Sharp, Gemma C. Granell, Raquel Tilling, Kate Relton, Caroline L. |
author_facet | Arathimos, Ryan Sharp, Gemma C. Granell, Raquel Tilling, Kate Relton, Caroline L. |
author_sort | Arathimos, Ryan |
collection | PubMed |
description | BACKGROUND: Levels of sex hormone-binding globulin (SHBG) and the androgen testosterone have been associated with risk of diseases throughout the lifecourse. Although both SHBG and testosterone have been shown to be highly heritable, only a fraction of that heritability has been explained by genetic studies. Epigenetic modifications such as DNA methylation may explain some of the missing heritability and could potentially inform biological knowledge of endocrine disease mechanisms involved in development of later life disease. Using data from the Avon Longitudinal Study of Parents and Children (ALSPAC), we explored cross-sectional associations of SHBG, total testosterone and bioavailable testosterone in childhood (males only) and adolescence (both males and females) with genome-wide DNA methylation. We also report associations of a SHBG polymorphism (rs12150660) with DNA methylation, which leads to differential levels of SHBG in carriers, as a genetic proxy of circulating SHBG levels. RESULTS: We identified several novel sites and genomic regions where levels of SHBG, total testosterone, and bioavailable testosterone were associated with DNA methylation, including one region associated with total testosterone in males (annotated to the KLHL31 gene) in both childhood and adolescence and a second region associated with bioavailable testosterone (annotated to the CMYA5 gene) at both time-points. We also identified one region where both SHBG and bioavailable testosterone in males in childhood (annotated to the ZNF718 gene) was associated with DNA methylation. CONCLUSION: Our findings have important implications in the understanding of the biological processes of SHBG and testosterone, with the potential for future work to determine the molecular mechanisms that could underpin these associations. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12863-018-0703-y) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-6295101 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-62951012018-12-18 Associations of sex hormone-binding globulin and testosterone with genome-wide DNA methylation Arathimos, Ryan Sharp, Gemma C. Granell, Raquel Tilling, Kate Relton, Caroline L. BMC Genet Research Article BACKGROUND: Levels of sex hormone-binding globulin (SHBG) and the androgen testosterone have been associated with risk of diseases throughout the lifecourse. Although both SHBG and testosterone have been shown to be highly heritable, only a fraction of that heritability has been explained by genetic studies. Epigenetic modifications such as DNA methylation may explain some of the missing heritability and could potentially inform biological knowledge of endocrine disease mechanisms involved in development of later life disease. Using data from the Avon Longitudinal Study of Parents and Children (ALSPAC), we explored cross-sectional associations of SHBG, total testosterone and bioavailable testosterone in childhood (males only) and adolescence (both males and females) with genome-wide DNA methylation. We also report associations of a SHBG polymorphism (rs12150660) with DNA methylation, which leads to differential levels of SHBG in carriers, as a genetic proxy of circulating SHBG levels. RESULTS: We identified several novel sites and genomic regions where levels of SHBG, total testosterone, and bioavailable testosterone were associated with DNA methylation, including one region associated with total testosterone in males (annotated to the KLHL31 gene) in both childhood and adolescence and a second region associated with bioavailable testosterone (annotated to the CMYA5 gene) at both time-points. We also identified one region where both SHBG and bioavailable testosterone in males in childhood (annotated to the ZNF718 gene) was associated with DNA methylation. CONCLUSION: Our findings have important implications in the understanding of the biological processes of SHBG and testosterone, with the potential for future work to determine the molecular mechanisms that could underpin these associations. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12863-018-0703-y) contains supplementary material, which is available to authorized users. BioMed Central 2018-12-14 /pmc/articles/PMC6295101/ /pubmed/30547757 http://dx.doi.org/10.1186/s12863-018-0703-y Text en © The Author(s). 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Article Arathimos, Ryan Sharp, Gemma C. Granell, Raquel Tilling, Kate Relton, Caroline L. Associations of sex hormone-binding globulin and testosterone with genome-wide DNA methylation |
title | Associations of sex hormone-binding globulin and testosterone with genome-wide DNA methylation |
title_full | Associations of sex hormone-binding globulin and testosterone with genome-wide DNA methylation |
title_fullStr | Associations of sex hormone-binding globulin and testosterone with genome-wide DNA methylation |
title_full_unstemmed | Associations of sex hormone-binding globulin and testosterone with genome-wide DNA methylation |
title_short | Associations of sex hormone-binding globulin and testosterone with genome-wide DNA methylation |
title_sort | associations of sex hormone-binding globulin and testosterone with genome-wide dna methylation |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6295101/ https://www.ncbi.nlm.nih.gov/pubmed/30547757 http://dx.doi.org/10.1186/s12863-018-0703-y |
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