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Genetic variations, reproductive aging, and breast cancer risk in African American and European American women: The Women's Circle of Health Study

Reproductive aging phenotypes, including age at menarche (AM) and age at natural menopause (ANM), are well-established risk factors for breast cancer. In recent years, many genetic variants have been identified in association with AM and ANM in genome-wide association studies among European populati...

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Autores principales: Coignet, Marie V., Zirpoli, Gary Robert, Roberts, Michelle R., Khoury, Thaer, Bandera, Elisa V., Zhu, Qianqian, Yao, Song
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5658184/
https://www.ncbi.nlm.nih.gov/pubmed/29073238
http://dx.doi.org/10.1371/journal.pone.0187205
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author Coignet, Marie V.
Zirpoli, Gary Robert
Roberts, Michelle R.
Khoury, Thaer
Bandera, Elisa V.
Zhu, Qianqian
Yao, Song
author_facet Coignet, Marie V.
Zirpoli, Gary Robert
Roberts, Michelle R.
Khoury, Thaer
Bandera, Elisa V.
Zhu, Qianqian
Yao, Song
author_sort Coignet, Marie V.
collection PubMed
description Reproductive aging phenotypes, including age at menarche (AM) and age at natural menopause (ANM), are well-established risk factors for breast cancer. In recent years, many genetic variants have been identified in association with AM and ANM in genome-wide association studies among European populations. Using data from the Women’s Circle of Health Study (WCHS) of 1,307 European-American (EA) and 1,365 African-American (AA) breast cancer cases and controls, we aimed to replicate 53 earlier GWAS variants for AM and ANM in AA and EA groups and to perform analyses on total and net reproductive lifespan (TRLS; NRLS). Breast cancer risk was also examined in relation to a polygenic risk score (PRS) for each of the reproductive aging phenotypes. We replicated a number of variants in EA women, including rs7759938 in LIN28B for AM and rs16991615 in MCM8 for ANM; whereas in the AA group, only one SNP (rs2947411 in TMEM18) for AM was directionally consistent and nominally significant. In analysis of TRLS and NRLS, several SNPs were significant, including rs466639 in RXRG that was associated with both phenotypes in both AA and EA groups. None of the PRS was associated with breast cancer risk. Given the paucity of data available among AA populations, our study contributes to the literature of genetics of reproductive aging in AA women and highlights the importance of cross population replication of GWAS variants.
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spelling pubmed-56581842017-11-09 Genetic variations, reproductive aging, and breast cancer risk in African American and European American women: The Women's Circle of Health Study Coignet, Marie V. Zirpoli, Gary Robert Roberts, Michelle R. Khoury, Thaer Bandera, Elisa V. Zhu, Qianqian Yao, Song PLoS One Research Article Reproductive aging phenotypes, including age at menarche (AM) and age at natural menopause (ANM), are well-established risk factors for breast cancer. In recent years, many genetic variants have been identified in association with AM and ANM in genome-wide association studies among European populations. Using data from the Women’s Circle of Health Study (WCHS) of 1,307 European-American (EA) and 1,365 African-American (AA) breast cancer cases and controls, we aimed to replicate 53 earlier GWAS variants for AM and ANM in AA and EA groups and to perform analyses on total and net reproductive lifespan (TRLS; NRLS). Breast cancer risk was also examined in relation to a polygenic risk score (PRS) for each of the reproductive aging phenotypes. We replicated a number of variants in EA women, including rs7759938 in LIN28B for AM and rs16991615 in MCM8 for ANM; whereas in the AA group, only one SNP (rs2947411 in TMEM18) for AM was directionally consistent and nominally significant. In analysis of TRLS and NRLS, several SNPs were significant, including rs466639 in RXRG that was associated with both phenotypes in both AA and EA groups. None of the PRS was associated with breast cancer risk. Given the paucity of data available among AA populations, our study contributes to the literature of genetics of reproductive aging in AA women and highlights the importance of cross population replication of GWAS variants. Public Library of Science 2017-10-26 /pmc/articles/PMC5658184/ /pubmed/29073238 http://dx.doi.org/10.1371/journal.pone.0187205 Text en © 2017 Coignet et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Coignet, Marie V.
Zirpoli, Gary Robert
Roberts, Michelle R.
Khoury, Thaer
Bandera, Elisa V.
Zhu, Qianqian
Yao, Song
Genetic variations, reproductive aging, and breast cancer risk in African American and European American women: The Women's Circle of Health Study
title Genetic variations, reproductive aging, and breast cancer risk in African American and European American women: The Women's Circle of Health Study
title_full Genetic variations, reproductive aging, and breast cancer risk in African American and European American women: The Women's Circle of Health Study
title_fullStr Genetic variations, reproductive aging, and breast cancer risk in African American and European American women: The Women's Circle of Health Study
title_full_unstemmed Genetic variations, reproductive aging, and breast cancer risk in African American and European American women: The Women's Circle of Health Study
title_short Genetic variations, reproductive aging, and breast cancer risk in African American and European American women: The Women's Circle of Health Study
title_sort genetic variations, reproductive aging, and breast cancer risk in african american and european american women: the women's circle of health study
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5658184/
https://www.ncbi.nlm.nih.gov/pubmed/29073238
http://dx.doi.org/10.1371/journal.pone.0187205
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