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Causal effects of genetically predicted endometriosis on breast cancer: a two-sample Mendelian randomization study

This study used a Mendelian randomization (MR) approach to investigate the causal relationship between genetically predicted endometriosis (EMS) and breast cancer risk. A total of 122,977 cases and 105,974 controls were included in the analysis, with gene-level summary data obtained from the Breast...

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Autores principales: Yan, Shuixin, Li, Jiadi, Chen, Jiafeng, Chen, Yan, Qiu, Yu, Zhou, Yuxin, Wu, Weizhu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10570324/
https://www.ncbi.nlm.nih.gov/pubmed/37828053
http://dx.doi.org/10.1038/s41598-023-43999-7
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author Yan, Shuixin
Li, Jiadi
Chen, Jiafeng
Chen, Yan
Qiu, Yu
Zhou, Yuxin
Wu, Weizhu
author_facet Yan, Shuixin
Li, Jiadi
Chen, Jiafeng
Chen, Yan
Qiu, Yu
Zhou, Yuxin
Wu, Weizhu
author_sort Yan, Shuixin
collection PubMed
description This study used a Mendelian randomization (MR) approach to investigate the causal relationship between genetically predicted endometriosis (EMS) and breast cancer risk. A total of 122,977 cases and 105,974 controls were included in the analysis, with gene-level summary data obtained from the Breast Cancer Association Consortium (BCAC). An inverse variance-weighting approach was applied to assess the causal relationship between EMS and breast cancer risk, and weighted median and MR-Egger regression methods were used to evaluate pleiotropy. Results showed a causal relationship between EMS and a decreased risk of overall breast cancer (odds ratio [OR] 0.95; 95% CI 0.90–0.99, p = 0.02). Furthermore, EMS was associated with a lower risk for estrogen receptor (ER)-positive breast cancer in a subgroup analysis based on immunohistochemistry type (OR 0.91; 95% CI 0.86–0.97, p = 0.005). However, there was no causal association between ER-negative breast cancer and survival (OR 1.00; 95% CI 0.94–1.06, p = 0.89). Pleiotropy was not observed. These findings provide evidence of a relationship between EMS and reduced breast cancer risk in invasive breast cancer overall and specific tissue types, and support the results of a previous observational study. Further research is needed to elucidate the mechanisms underlying this association.
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spelling pubmed-105703242023-10-14 Causal effects of genetically predicted endometriosis on breast cancer: a two-sample Mendelian randomization study Yan, Shuixin Li, Jiadi Chen, Jiafeng Chen, Yan Qiu, Yu Zhou, Yuxin Wu, Weizhu Sci Rep Article This study used a Mendelian randomization (MR) approach to investigate the causal relationship between genetically predicted endometriosis (EMS) and breast cancer risk. A total of 122,977 cases and 105,974 controls were included in the analysis, with gene-level summary data obtained from the Breast Cancer Association Consortium (BCAC). An inverse variance-weighting approach was applied to assess the causal relationship between EMS and breast cancer risk, and weighted median and MR-Egger regression methods were used to evaluate pleiotropy. Results showed a causal relationship between EMS and a decreased risk of overall breast cancer (odds ratio [OR] 0.95; 95% CI 0.90–0.99, p = 0.02). Furthermore, EMS was associated with a lower risk for estrogen receptor (ER)-positive breast cancer in a subgroup analysis based on immunohistochemistry type (OR 0.91; 95% CI 0.86–0.97, p = 0.005). However, there was no causal association between ER-negative breast cancer and survival (OR 1.00; 95% CI 0.94–1.06, p = 0.89). Pleiotropy was not observed. These findings provide evidence of a relationship between EMS and reduced breast cancer risk in invasive breast cancer overall and specific tissue types, and support the results of a previous observational study. Further research is needed to elucidate the mechanisms underlying this association. Nature Publishing Group UK 2023-10-12 /pmc/articles/PMC10570324/ /pubmed/37828053 http://dx.doi.org/10.1038/s41598-023-43999-7 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This 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/) .
spellingShingle Article
Yan, Shuixin
Li, Jiadi
Chen, Jiafeng
Chen, Yan
Qiu, Yu
Zhou, Yuxin
Wu, Weizhu
Causal effects of genetically predicted endometriosis on breast cancer: a two-sample Mendelian randomization study
title Causal effects of genetically predicted endometriosis on breast cancer: a two-sample Mendelian randomization study
title_full Causal effects of genetically predicted endometriosis on breast cancer: a two-sample Mendelian randomization study
title_fullStr Causal effects of genetically predicted endometriosis on breast cancer: a two-sample Mendelian randomization study
title_full_unstemmed Causal effects of genetically predicted endometriosis on breast cancer: a two-sample Mendelian randomization study
title_short Causal effects of genetically predicted endometriosis on breast cancer: a two-sample Mendelian randomization study
title_sort causal effects of genetically predicted endometriosis on breast cancer: a two-sample mendelian randomization study
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10570324/
https://www.ncbi.nlm.nih.gov/pubmed/37828053
http://dx.doi.org/10.1038/s41598-023-43999-7
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