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Using human genetics to understand the disease impacts of testosterone in men and women
Testosterone supplementation is commonly used for its effects on sexual function, bone health and body composition, yet its effects on disease outcomes are unknown. To better understand this, we identified genetic determinants of testosterone levels and related sex hormone traits in 425,097 UK Bioba...
Autores principales: | , , , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7025895/ https://www.ncbi.nlm.nih.gov/pubmed/32042192 http://dx.doi.org/10.1038/s41591-020-0751-5 |
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author | Ruth, Katherine S Day, Felix R Tyrrell, Jessica Thompson, Deborah J Wood, Andrew R Mahajan, Anubha Beaumont, Robin N Wittemans, Laura Martin, Susan Busch, Alexander S. Erzurumluoglu, A. Mesut Hollis, Benjamin O’Mara, Tracy A. McCarthy, Mark I Langenberg, Claudia Easton, Douglas F Wareham, Nicholas J Burgess, Stephen Murray, Anna Ong, Ken K Frayling, Timothy M Perry, John R.B. |
author_facet | Ruth, Katherine S Day, Felix R Tyrrell, Jessica Thompson, Deborah J Wood, Andrew R Mahajan, Anubha Beaumont, Robin N Wittemans, Laura Martin, Susan Busch, Alexander S. Erzurumluoglu, A. Mesut Hollis, Benjamin O’Mara, Tracy A. McCarthy, Mark I Langenberg, Claudia Easton, Douglas F Wareham, Nicholas J Burgess, Stephen Murray, Anna Ong, Ken K Frayling, Timothy M Perry, John R.B. |
author_sort | Ruth, Katherine S |
collection | PubMed |
description | Testosterone supplementation is commonly used for its effects on sexual function, bone health and body composition, yet its effects on disease outcomes are unknown. To better understand this, we identified genetic determinants of testosterone levels and related sex hormone traits in 425,097 UK Biobank study participants. Using 2,571 genome-wide significant associations, we demonstrate the genetic determinants of testosterone levels are substantially different between sexes, and that genetically higher testosterone is harmful for metabolic diseases in women but beneficial in men. For example, a genetically determined 1-standard deviation higher testosterone increases the risks of Type 2 diabetes (T2D) (OR=1.37 [1.22–1.53]) and polycystic ovary syndrome (OR=1.51 [1.33–1.72]) in women, but reduces T2D risk in men (OR=0.86 [0.76–0.98]). We also show adverse effects of higher testosterone on breast and endometrial cancers in women, and prostate cancer in men. Our findings provide insights into the disease impacts of testosterone and highlight the importance of sex-specific genetic analyses. |
format | Online Article Text |
id | pubmed-7025895 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
record_format | MEDLINE/PubMed |
spelling | pubmed-70258952020-08-10 Using human genetics to understand the disease impacts of testosterone in men and women Ruth, Katherine S Day, Felix R Tyrrell, Jessica Thompson, Deborah J Wood, Andrew R Mahajan, Anubha Beaumont, Robin N Wittemans, Laura Martin, Susan Busch, Alexander S. Erzurumluoglu, A. Mesut Hollis, Benjamin O’Mara, Tracy A. McCarthy, Mark I Langenberg, Claudia Easton, Douglas F Wareham, Nicholas J Burgess, Stephen Murray, Anna Ong, Ken K Frayling, Timothy M Perry, John R.B. Nat Med Article Testosterone supplementation is commonly used for its effects on sexual function, bone health and body composition, yet its effects on disease outcomes are unknown. To better understand this, we identified genetic determinants of testosterone levels and related sex hormone traits in 425,097 UK Biobank study participants. Using 2,571 genome-wide significant associations, we demonstrate the genetic determinants of testosterone levels are substantially different between sexes, and that genetically higher testosterone is harmful for metabolic diseases in women but beneficial in men. For example, a genetically determined 1-standard deviation higher testosterone increases the risks of Type 2 diabetes (T2D) (OR=1.37 [1.22–1.53]) and polycystic ovary syndrome (OR=1.51 [1.33–1.72]) in women, but reduces T2D risk in men (OR=0.86 [0.76–0.98]). We also show adverse effects of higher testosterone on breast and endometrial cancers in women, and prostate cancer in men. Our findings provide insights into the disease impacts of testosterone and highlight the importance of sex-specific genetic analyses. 2020-02-10 2020-02 /pmc/articles/PMC7025895/ /pubmed/32042192 http://dx.doi.org/10.1038/s41591-020-0751-5 Text en http://www.nature.com/authors/editorial_policies/license.html#terms Users may view, print, copy, and download text and data-mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use:http://www.nature.com/authors/editorial_policies/license.html#terms |
spellingShingle | Article Ruth, Katherine S Day, Felix R Tyrrell, Jessica Thompson, Deborah J Wood, Andrew R Mahajan, Anubha Beaumont, Robin N Wittemans, Laura Martin, Susan Busch, Alexander S. Erzurumluoglu, A. Mesut Hollis, Benjamin O’Mara, Tracy A. McCarthy, Mark I Langenberg, Claudia Easton, Douglas F Wareham, Nicholas J Burgess, Stephen Murray, Anna Ong, Ken K Frayling, Timothy M Perry, John R.B. Using human genetics to understand the disease impacts of testosterone in men and women |
title | Using human genetics to understand the disease impacts of testosterone in men and women |
title_full | Using human genetics to understand the disease impacts of testosterone in men and women |
title_fullStr | Using human genetics to understand the disease impacts of testosterone in men and women |
title_full_unstemmed | Using human genetics to understand the disease impacts of testosterone in men and women |
title_short | Using human genetics to understand the disease impacts of testosterone in men and women |
title_sort | using human genetics to understand the disease impacts of testosterone in men and women |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7025895/ https://www.ncbi.nlm.nih.gov/pubmed/32042192 http://dx.doi.org/10.1038/s41591-020-0751-5 |
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