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Gut microbiome and pancreatic cancer cachexia: An evolving relationship
Nearly 80% of patients with pancreatic ductal adenocarcinoma (PDAC) develop cachexia along their disease course. Cachexia is characterized by progressive weight loss, muscle wasting, and systemic inflammation and has been linked to poorer outcomes and impairments in quality of life. Management of PD...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Baishideng Publishing Group Inc
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9305570/ https://www.ncbi.nlm.nih.gov/pubmed/36051103 http://dx.doi.org/10.4251/wjgo.v14.i7.1218 |
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author | Hendifar, Andrew Akinsola, Rasaq Muranaka, Hayato Osipov, Arsen Thomassian, Shant Moshayedi, Natalie Yang, Julianne Jacobs, Jonathan Devkota, Suzanne Bhowmick, Neil Gong, Jun |
author_facet | Hendifar, Andrew Akinsola, Rasaq Muranaka, Hayato Osipov, Arsen Thomassian, Shant Moshayedi, Natalie Yang, Julianne Jacobs, Jonathan Devkota, Suzanne Bhowmick, Neil Gong, Jun |
author_sort | Hendifar, Andrew |
collection | PubMed |
description | Nearly 80% of patients with pancreatic ductal adenocarcinoma (PDAC) develop cachexia along their disease course. Cachexia is characterized by progressive weight loss, muscle wasting, and systemic inflammation and has been linked to poorer outcomes and impairments in quality of life. Management of PDAC cachexia has historically involved a multidisciplinary effort comprised of nutritional support, pancreatic enzyme replacement therapy, and/or pharmacologic interventions. Despite current interventions to mitigate PDAC cachexia, a significant proportion of patients continue to die from complications associated with cachexia underscoring the need for novel insights and treatments for this syndrome. We highlight the feasibility and effectiveness of a recent enteral feeding prospective trial at our institution to improve cachexia outcomes in patients with advanced PDAC. Additionally, we were among the first to characterize the stool microbiome composition in patients with advanced PDAC receiving enteral feeding for the treatment of cachexia. Novel insights into the relationship between enteral nutritional support, cachexia, and the gut microbiome are presented. These promising results are discussed in the context of a potential ability to modulate the stool microbiome as a new interventional strategy to mitigate PDAC cachexia. |
format | Online Article Text |
id | pubmed-9305570 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Baishideng Publishing Group Inc |
record_format | MEDLINE/PubMed |
spelling | pubmed-93055702022-08-31 Gut microbiome and pancreatic cancer cachexia: An evolving relationship Hendifar, Andrew Akinsola, Rasaq Muranaka, Hayato Osipov, Arsen Thomassian, Shant Moshayedi, Natalie Yang, Julianne Jacobs, Jonathan Devkota, Suzanne Bhowmick, Neil Gong, Jun World J Gastrointest Oncol Frontier Nearly 80% of patients with pancreatic ductal adenocarcinoma (PDAC) develop cachexia along their disease course. Cachexia is characterized by progressive weight loss, muscle wasting, and systemic inflammation and has been linked to poorer outcomes and impairments in quality of life. Management of PDAC cachexia has historically involved a multidisciplinary effort comprised of nutritional support, pancreatic enzyme replacement therapy, and/or pharmacologic interventions. Despite current interventions to mitigate PDAC cachexia, a significant proportion of patients continue to die from complications associated with cachexia underscoring the need for novel insights and treatments for this syndrome. We highlight the feasibility and effectiveness of a recent enteral feeding prospective trial at our institution to improve cachexia outcomes in patients with advanced PDAC. Additionally, we were among the first to characterize the stool microbiome composition in patients with advanced PDAC receiving enteral feeding for the treatment of cachexia. Novel insights into the relationship between enteral nutritional support, cachexia, and the gut microbiome are presented. These promising results are discussed in the context of a potential ability to modulate the stool microbiome as a new interventional strategy to mitigate PDAC cachexia. Baishideng Publishing Group Inc 2022-07-15 2022-07-15 /pmc/articles/PMC9305570/ /pubmed/36051103 http://dx.doi.org/10.4251/wjgo.v14.i7.1218 Text en ©The Author(s) 2022. Published by Baishideng Publishing Group Inc. All rights reserved. https://creativecommons.org/licenses/by-nc/4.0/This article is an open-access article that was selected by an in-house editor and fully peer-reviewed by external reviewers. It is distributed in accordance with the Creative Commons Attribution NonCommercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: https://creativecommons.org/Licenses/by-nc/4.0/ |
spellingShingle | Frontier Hendifar, Andrew Akinsola, Rasaq Muranaka, Hayato Osipov, Arsen Thomassian, Shant Moshayedi, Natalie Yang, Julianne Jacobs, Jonathan Devkota, Suzanne Bhowmick, Neil Gong, Jun Gut microbiome and pancreatic cancer cachexia: An evolving relationship |
title | Gut microbiome and pancreatic cancer cachexia: An evolving relationship |
title_full | Gut microbiome and pancreatic cancer cachexia: An evolving relationship |
title_fullStr | Gut microbiome and pancreatic cancer cachexia: An evolving relationship |
title_full_unstemmed | Gut microbiome and pancreatic cancer cachexia: An evolving relationship |
title_short | Gut microbiome and pancreatic cancer cachexia: An evolving relationship |
title_sort | gut microbiome and pancreatic cancer cachexia: an evolving relationship |
topic | Frontier |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9305570/ https://www.ncbi.nlm.nih.gov/pubmed/36051103 http://dx.doi.org/10.4251/wjgo.v14.i7.1218 |
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