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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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Detalles Bibliográficos
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
Descripción
Sumario: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.