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Serum iron status and the risk of breast cancer in the European population: a two-sample Mendelian randomisation study

BACKGROUND: Previous observational studies have provided conflicting results on the association between serum iron status and the risk of breast cancer. Considering the relevance of this relationship to breast cancer prevention, its elucidation is warranted. OBJECT: We used a two-sample Mendelian ra...

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Autores principales: Hou, Chenyang, Hou, Qingzhi, Xie, Xing, Wang, Huifeng, Chen, Yueliang, Lu, Tingxi, Wu, Qunying, Liang, Yongcong, Hu, Yanling, Mao, Yuang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8259019/
https://www.ncbi.nlm.nih.gov/pubmed/34229617
http://dx.doi.org/10.1186/s12263-021-00691-7
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author Hou, Chenyang
Hou, Qingzhi
Xie, Xing
Wang, Huifeng
Chen, Yueliang
Lu, Tingxi
Wu, Qunying
Liang, Yongcong
Hu, Yanling
Mao, Yuang
author_facet Hou, Chenyang
Hou, Qingzhi
Xie, Xing
Wang, Huifeng
Chen, Yueliang
Lu, Tingxi
Wu, Qunying
Liang, Yongcong
Hu, Yanling
Mao, Yuang
author_sort Hou, Chenyang
collection PubMed
description BACKGROUND: Previous observational studies have provided conflicting results on the association between serum iron status and the risk of breast cancer. Considering the relevance of this relationship to breast cancer prevention, its elucidation is warranted. OBJECT: We used a two-sample Mendelian randomisation (MR) study to explore the causal relationship between serum iron status and the risk of breast cancer. METHOD: To select single nucleotide polymorphisms (SNPs) that could be used as instrumental variables for iron status, we used the Genetics of Iron Status consortium, which includes 11 discovery and 8 replication cohorts, encompassing 48,972 individuals of European descent. Moreover, we used the OncoArray network to select SNPs that could be considered instrumental variables for the outcome of interest (breast cancer); this dataset included 122,977 individuals of European descent with breast cancer and 105,974 peers without breast cancer. Both conservative (SNPs associated with overall iron status markers) and liberal (SNPs associated with the levels of at least one iron status marker) approaches were used as part of the MR analysis. For the former, we used an inverse-variance weighted (IVW) method, whereas for the latter, we used the IVW, MR-Egger regression, weighted median and simple mode methods. RESULTS: When the conservative approach was used, iron status showed no significant association with the risk of breast cancer or any of its subtypes. However, when the liberal approach was used, transferrin levels were found to be positively associated with the risk of ER-negative breast cancer based on the simple mode method (OR for MR, 1.225; 95% CI, 1.064, 1.410; P = 0.030). Nevertheless, the levels of the other iron status markers showed no association with the risk of breast cancer or its subtypes (P > 0.05). CONCLUSION: In our MR study, the liberal approach suggested that changes in the concentration of transferrin could increase the risk of ER-negative breast cancer, although the levels of other iron status markers had no effect on the risk of breast cancer or its subtypes. This should be verified in future studies. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12263-021-00691-7.
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spelling pubmed-82590192021-07-07 Serum iron status and the risk of breast cancer in the European population: a two-sample Mendelian randomisation study Hou, Chenyang Hou, Qingzhi Xie, Xing Wang, Huifeng Chen, Yueliang Lu, Tingxi Wu, Qunying Liang, Yongcong Hu, Yanling Mao, Yuang Genes Nutr Research BACKGROUND: Previous observational studies have provided conflicting results on the association between serum iron status and the risk of breast cancer. Considering the relevance of this relationship to breast cancer prevention, its elucidation is warranted. OBJECT: We used a two-sample Mendelian randomisation (MR) study to explore the causal relationship between serum iron status and the risk of breast cancer. METHOD: To select single nucleotide polymorphisms (SNPs) that could be used as instrumental variables for iron status, we used the Genetics of Iron Status consortium, which includes 11 discovery and 8 replication cohorts, encompassing 48,972 individuals of European descent. Moreover, we used the OncoArray network to select SNPs that could be considered instrumental variables for the outcome of interest (breast cancer); this dataset included 122,977 individuals of European descent with breast cancer and 105,974 peers without breast cancer. Both conservative (SNPs associated with overall iron status markers) and liberal (SNPs associated with the levels of at least one iron status marker) approaches were used as part of the MR analysis. For the former, we used an inverse-variance weighted (IVW) method, whereas for the latter, we used the IVW, MR-Egger regression, weighted median and simple mode methods. RESULTS: When the conservative approach was used, iron status showed no significant association with the risk of breast cancer or any of its subtypes. However, when the liberal approach was used, transferrin levels were found to be positively associated with the risk of ER-negative breast cancer based on the simple mode method (OR for MR, 1.225; 95% CI, 1.064, 1.410; P = 0.030). Nevertheless, the levels of the other iron status markers showed no association with the risk of breast cancer or its subtypes (P > 0.05). CONCLUSION: In our MR study, the liberal approach suggested that changes in the concentration of transferrin could increase the risk of ER-negative breast cancer, although the levels of other iron status markers had no effect on the risk of breast cancer or its subtypes. This should be verified in future studies. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12263-021-00691-7. BioMed Central 2021-07-06 /pmc/articles/PMC8259019/ /pubmed/34229617 http://dx.doi.org/10.1186/s12263-021-00691-7 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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 Research
Hou, Chenyang
Hou, Qingzhi
Xie, Xing
Wang, Huifeng
Chen, Yueliang
Lu, Tingxi
Wu, Qunying
Liang, Yongcong
Hu, Yanling
Mao, Yuang
Serum iron status and the risk of breast cancer in the European population: a two-sample Mendelian randomisation study
title Serum iron status and the risk of breast cancer in the European population: a two-sample Mendelian randomisation study
title_full Serum iron status and the risk of breast cancer in the European population: a two-sample Mendelian randomisation study
title_fullStr Serum iron status and the risk of breast cancer in the European population: a two-sample Mendelian randomisation study
title_full_unstemmed Serum iron status and the risk of breast cancer in the European population: a two-sample Mendelian randomisation study
title_short Serum iron status and the risk of breast cancer in the European population: a two-sample Mendelian randomisation study
title_sort serum iron status and the risk of breast cancer in the european population: a two-sample mendelian randomisation study
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8259019/
https://www.ncbi.nlm.nih.gov/pubmed/34229617
http://dx.doi.org/10.1186/s12263-021-00691-7
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