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Physiologic intestinal (18)F-FDG uptake is associated with alteration of gut microbiota and proinflammatory cytokine levels in breast cancer

The clinical significance of physiologic Fluorine-18-fluorodeoxyglucose ((18)F-FDG) intestinal uptake (IU) based on the predicted link with gut microbiota dysbiosis and inflammatory cytokine production was investigated in a cohort of breast cancer patients. A total of 114 patients were visually clas...

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Autores principales: Yoon, Hai-Jeon, Kim, Han-Na, Bang, Ji-In, Lim, Woosung, Moon, Byung In, Paik, Nam Sun, Kim, Bom Sahn, Kim, Hyung-Lae
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6892830/
https://www.ncbi.nlm.nih.gov/pubmed/31797893
http://dx.doi.org/10.1038/s41598-019-54680-3
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author Yoon, Hai-Jeon
Kim, Han-Na
Bang, Ji-In
Lim, Woosung
Moon, Byung In
Paik, Nam Sun
Kim, Bom Sahn
Kim, Hyung-Lae
author_facet Yoon, Hai-Jeon
Kim, Han-Na
Bang, Ji-In
Lim, Woosung
Moon, Byung In
Paik, Nam Sun
Kim, Bom Sahn
Kim, Hyung-Lae
author_sort Yoon, Hai-Jeon
collection PubMed
description The clinical significance of physiologic Fluorine-18-fluorodeoxyglucose ((18)F-FDG) intestinal uptake (IU) based on the predicted link with gut microbiota dysbiosis and inflammatory cytokine production was investigated in a cohort of breast cancer patients. A total of 114 patients were visually classified into the lower or higher IU group. The maximum and mean standardized uptake values of total bowel (TB SUV(max) and TB SUV(mean)) were measured. The gut microbial abundance of the Citrobacter genus of the Enterobacteriaceae family showed a significant positive correlation with TB SUV(max) and TB SUV(mean) (q = 0.021 and q = 0.010). The unclassified Ruminococcaceae showed a significant negative correlation with TB SUV(max) (q = 0.010). The level of tumor necrosis factor alpha (TNF-α) was significantly increased in the high IU group (p = 0.017). The TNF-α levels showed a significant positive correlation with TB SUV(max) (rho = 0.220 and p = 0.018) and TB SUV(mean) (rho = 0.250 and p = 0.007). Therefore, our findings suggest that the physiologic intestinal uptake may reflect subclinical inflammation and differences in the composition of the gut microbiome in breast cancer patients.
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spelling pubmed-68928302019-12-10 Physiologic intestinal (18)F-FDG uptake is associated with alteration of gut microbiota and proinflammatory cytokine levels in breast cancer Yoon, Hai-Jeon Kim, Han-Na Bang, Ji-In Lim, Woosung Moon, Byung In Paik, Nam Sun Kim, Bom Sahn Kim, Hyung-Lae Sci Rep Article The clinical significance of physiologic Fluorine-18-fluorodeoxyglucose ((18)F-FDG) intestinal uptake (IU) based on the predicted link with gut microbiota dysbiosis and inflammatory cytokine production was investigated in a cohort of breast cancer patients. A total of 114 patients were visually classified into the lower or higher IU group. The maximum and mean standardized uptake values of total bowel (TB SUV(max) and TB SUV(mean)) were measured. The gut microbial abundance of the Citrobacter genus of the Enterobacteriaceae family showed a significant positive correlation with TB SUV(max) and TB SUV(mean) (q = 0.021 and q = 0.010). The unclassified Ruminococcaceae showed a significant negative correlation with TB SUV(max) (q = 0.010). The level of tumor necrosis factor alpha (TNF-α) was significantly increased in the high IU group (p = 0.017). The TNF-α levels showed a significant positive correlation with TB SUV(max) (rho = 0.220 and p = 0.018) and TB SUV(mean) (rho = 0.250 and p = 0.007). Therefore, our findings suggest that the physiologic intestinal uptake may reflect subclinical inflammation and differences in the composition of the gut microbiome in breast cancer patients. Nature Publishing Group UK 2019-12-04 /pmc/articles/PMC6892830/ /pubmed/31797893 http://dx.doi.org/10.1038/s41598-019-54680-3 Text en © The Author(s) 2019 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Yoon, Hai-Jeon
Kim, Han-Na
Bang, Ji-In
Lim, Woosung
Moon, Byung In
Paik, Nam Sun
Kim, Bom Sahn
Kim, Hyung-Lae
Physiologic intestinal (18)F-FDG uptake is associated with alteration of gut microbiota and proinflammatory cytokine levels in breast cancer
title Physiologic intestinal (18)F-FDG uptake is associated with alteration of gut microbiota and proinflammatory cytokine levels in breast cancer
title_full Physiologic intestinal (18)F-FDG uptake is associated with alteration of gut microbiota and proinflammatory cytokine levels in breast cancer
title_fullStr Physiologic intestinal (18)F-FDG uptake is associated with alteration of gut microbiota and proinflammatory cytokine levels in breast cancer
title_full_unstemmed Physiologic intestinal (18)F-FDG uptake is associated with alteration of gut microbiota and proinflammatory cytokine levels in breast cancer
title_short Physiologic intestinal (18)F-FDG uptake is associated with alteration of gut microbiota and proinflammatory cytokine levels in breast cancer
title_sort physiologic intestinal (18)f-fdg uptake is associated with alteration of gut microbiota and proinflammatory cytokine levels in breast cancer
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6892830/
https://www.ncbi.nlm.nih.gov/pubmed/31797893
http://dx.doi.org/10.1038/s41598-019-54680-3
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