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Impacts of breast cancer and chemotherapy on gut microbiome, cognitive functioning, and mood relative to healthy controls
Women diagnosed with breast cancer undergoing chemotherapy experience cognitive impairment, symptoms of anxiety and depression, and physical side effects including disruption in the diversity and community composition of the gut microbiome. To date, there is limited research exploring the associatio...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9664046/ https://www.ncbi.nlm.nih.gov/pubmed/36380060 http://dx.doi.org/10.1038/s41598-022-23793-7 |
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author | Bilenduke, Emily Sterrett, John D. Ranby, Krista W. Borges, Virginia F. Grigsby, Jim Carr, Alaina L. Kilbourn, Kristin Lowry, Christopher A. |
author_facet | Bilenduke, Emily Sterrett, John D. Ranby, Krista W. Borges, Virginia F. Grigsby, Jim Carr, Alaina L. Kilbourn, Kristin Lowry, Christopher A. |
author_sort | Bilenduke, Emily |
collection | PubMed |
description | Women diagnosed with breast cancer undergoing chemotherapy experience cognitive impairment, symptoms of anxiety and depression, and physical side effects including disruption in the diversity and community composition of the gut microbiome. To date, there is limited research exploring the associations among these specific challenges. The present cross-sectional study explored the associations of self-reported cognitive functioning, depression, and anxiety symptoms, and gut microbiome diversity and community composition in women who were diagnosed with and undergoing chemotherapy treatment for breast cancer (BC) compared to cancer-free healthy controls (HC). The BC group displayed higher rates of cognitive dysfunction (p < 0.001) and depressive symptoms (p < 0.05) relative to HC. There was a significant difference in microbiome community composition between BC and HC, particularly characterized by a decreased relative abundance of the mucin-degrading genus Akkermansia in BC compared to HC (p < 0.05). Association models identified significant associations among group, cognitive, depression, and microbiome variables (p < 0.001). Overall, the study identified that BC participants experienced significant differences in self-reported cognitive functioning, self-reported depression symptoms, microbiome community composition, and mucin-degrading bacteria of the gut-mucosal barrier, relative to HC. The present study is consistent with the hypothesis that gut microbiome community composition impacts a woman’s experience with breast cancer and treatment suggesting that microbiome-based interventions have potential for improving quality of life outcomes in individuals with breast cancer. |
format | Online Article Text |
id | pubmed-9664046 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-96640462022-11-14 Impacts of breast cancer and chemotherapy on gut microbiome, cognitive functioning, and mood relative to healthy controls Bilenduke, Emily Sterrett, John D. Ranby, Krista W. Borges, Virginia F. Grigsby, Jim Carr, Alaina L. Kilbourn, Kristin Lowry, Christopher A. Sci Rep Article Women diagnosed with breast cancer undergoing chemotherapy experience cognitive impairment, symptoms of anxiety and depression, and physical side effects including disruption in the diversity and community composition of the gut microbiome. To date, there is limited research exploring the associations among these specific challenges. The present cross-sectional study explored the associations of self-reported cognitive functioning, depression, and anxiety symptoms, and gut microbiome diversity and community composition in women who were diagnosed with and undergoing chemotherapy treatment for breast cancer (BC) compared to cancer-free healthy controls (HC). The BC group displayed higher rates of cognitive dysfunction (p < 0.001) and depressive symptoms (p < 0.05) relative to HC. There was a significant difference in microbiome community composition between BC and HC, particularly characterized by a decreased relative abundance of the mucin-degrading genus Akkermansia in BC compared to HC (p < 0.05). Association models identified significant associations among group, cognitive, depression, and microbiome variables (p < 0.001). Overall, the study identified that BC participants experienced significant differences in self-reported cognitive functioning, self-reported depression symptoms, microbiome community composition, and mucin-degrading bacteria of the gut-mucosal barrier, relative to HC. The present study is consistent with the hypothesis that gut microbiome community composition impacts a woman’s experience with breast cancer and treatment suggesting that microbiome-based interventions have potential for improving quality of life outcomes in individuals with breast cancer. Nature Publishing Group UK 2022-11-15 /pmc/articles/PMC9664046/ /pubmed/36380060 http://dx.doi.org/10.1038/s41598-022-23793-7 Text en © The Author(s) 2022 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 Bilenduke, Emily Sterrett, John D. Ranby, Krista W. Borges, Virginia F. Grigsby, Jim Carr, Alaina L. Kilbourn, Kristin Lowry, Christopher A. Impacts of breast cancer and chemotherapy on gut microbiome, cognitive functioning, and mood relative to healthy controls |
title | Impacts of breast cancer and chemotherapy on gut microbiome, cognitive functioning, and mood relative to healthy controls |
title_full | Impacts of breast cancer and chemotherapy on gut microbiome, cognitive functioning, and mood relative to healthy controls |
title_fullStr | Impacts of breast cancer and chemotherapy on gut microbiome, cognitive functioning, and mood relative to healthy controls |
title_full_unstemmed | Impacts of breast cancer and chemotherapy on gut microbiome, cognitive functioning, and mood relative to healthy controls |
title_short | Impacts of breast cancer and chemotherapy on gut microbiome, cognitive functioning, and mood relative to healthy controls |
title_sort | impacts of breast cancer and chemotherapy on gut microbiome, cognitive functioning, and mood relative to healthy controls |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9664046/ https://www.ncbi.nlm.nih.gov/pubmed/36380060 http://dx.doi.org/10.1038/s41598-022-23793-7 |
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