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Joint Effect of Genotypic and Phenotypic Features of Reproductive Factors on Endometrial Cancer Risk

Prolonged estrogen exposure is believed to be the major cause of endometrial cancer. As possible markers of estrogen exposure, various menstrual and reproductive features, e.g., ages at menarche and menopause, are found to be associated with endometrial cancer risk. In order to assess their combined...

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Autores principales: Wang, Zhanwei, Risch, Harvey, Lu, Lingeng, Irwin, Melinda L., Mayne, Susan, Schwartz, Peter, Rutherford, Thomas, De Vivo, Immaculata, Yu, Herbert
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4620445/
https://www.ncbi.nlm.nih.gov/pubmed/26498156
http://dx.doi.org/10.1038/srep15582
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author Wang, Zhanwei
Risch, Harvey
Lu, Lingeng
Irwin, Melinda L.
Mayne, Susan
Schwartz, Peter
Rutherford, Thomas
De Vivo, Immaculata
Yu, Herbert
author_facet Wang, Zhanwei
Risch, Harvey
Lu, Lingeng
Irwin, Melinda L.
Mayne, Susan
Schwartz, Peter
Rutherford, Thomas
De Vivo, Immaculata
Yu, Herbert
author_sort Wang, Zhanwei
collection PubMed
description Prolonged estrogen exposure is believed to be the major cause of endometrial cancer. As possible markers of estrogen exposure, various menstrual and reproductive features, e.g., ages at menarche and menopause, are found to be associated with endometrial cancer risk. In order to assess their combined effects on endometrial cancer, we created the total number of menstrual cycles (TNMC) that a woman experienced during her life or up to the time of study and two genetic risk scores, GRS1 for age at menarche and GRS2 for age at menopause. Comparing 482 endometrial cancer patients with 571 population controls, we found TNMC was associated with endometrial cancer risk and that the association remained statistically significant after adjustment for obesity and other potential confounders. Risk increased by about 2.5% for every additional 10 menstrual-cycles. The study also showed that high GRS1 was associated with increased risk. This relationship, however, was attenuated after adjustment for obesity. Our study further indicated women with high TNMC and GRS1 had twice the risk of endometrial cancer compared to those low in both indices. Our results provided additional support to the involvement of estrogen exposure in endometrial cancer risk with regard to genetic background and lifestyle features.
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spelling pubmed-46204452015-10-29 Joint Effect of Genotypic and Phenotypic Features of Reproductive Factors on Endometrial Cancer Risk Wang, Zhanwei Risch, Harvey Lu, Lingeng Irwin, Melinda L. Mayne, Susan Schwartz, Peter Rutherford, Thomas De Vivo, Immaculata Yu, Herbert Sci Rep Article Prolonged estrogen exposure is believed to be the major cause of endometrial cancer. As possible markers of estrogen exposure, various menstrual and reproductive features, e.g., ages at menarche and menopause, are found to be associated with endometrial cancer risk. In order to assess their combined effects on endometrial cancer, we created the total number of menstrual cycles (TNMC) that a woman experienced during her life or up to the time of study and two genetic risk scores, GRS1 for age at menarche and GRS2 for age at menopause. Comparing 482 endometrial cancer patients with 571 population controls, we found TNMC was associated with endometrial cancer risk and that the association remained statistically significant after adjustment for obesity and other potential confounders. Risk increased by about 2.5% for every additional 10 menstrual-cycles. The study also showed that high GRS1 was associated with increased risk. This relationship, however, was attenuated after adjustment for obesity. Our study further indicated women with high TNMC and GRS1 had twice the risk of endometrial cancer compared to those low in both indices. Our results provided additional support to the involvement of estrogen exposure in endometrial cancer risk with regard to genetic background and lifestyle features. Nature Publishing Group 2015-10-26 /pmc/articles/PMC4620445/ /pubmed/26498156 http://dx.doi.org/10.1038/srep15582 Text en Copyright © 2015, Macmillan Publishers Limited 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
Wang, Zhanwei
Risch, Harvey
Lu, Lingeng
Irwin, Melinda L.
Mayne, Susan
Schwartz, Peter
Rutherford, Thomas
De Vivo, Immaculata
Yu, Herbert
Joint Effect of Genotypic and Phenotypic Features of Reproductive Factors on Endometrial Cancer Risk
title Joint Effect of Genotypic and Phenotypic Features of Reproductive Factors on Endometrial Cancer Risk
title_full Joint Effect of Genotypic and Phenotypic Features of Reproductive Factors on Endometrial Cancer Risk
title_fullStr Joint Effect of Genotypic and Phenotypic Features of Reproductive Factors on Endometrial Cancer Risk
title_full_unstemmed Joint Effect of Genotypic and Phenotypic Features of Reproductive Factors on Endometrial Cancer Risk
title_short Joint Effect of Genotypic and Phenotypic Features of Reproductive Factors on Endometrial Cancer Risk
title_sort joint effect of genotypic and phenotypic features of reproductive factors on endometrial cancer risk
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4620445/
https://www.ncbi.nlm.nih.gov/pubmed/26498156
http://dx.doi.org/10.1038/srep15582
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