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Gut Dysbiosis Associated with Antibiotics and Disease Severity and Its Relation to Mortality in Critically Ill Patients

BACKGROUND: The gut microbiota are reported to be altered in critical illness. The pattern and impact of dysbiosis on prognosis has not been thoroughly investigated in the ICU setting. AIMS: We aimed to evaluate changes in the gut microbiota of ICU patients via 16S rRNA gene deep sequencing, assess...

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Autores principales: Ojima, Masahiro, Shimizu, Kentaro, Motooka, Daisuke, Ishihara, Takuma, Nakamura, Shota, Shintani, Ayumi, Ogura, Hiroshi, Iida, Tetsuya, Yoshiya, Kazuhisa, Shimazu, Takeshi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer US 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8090918/
https://www.ncbi.nlm.nih.gov/pubmed/33939152
http://dx.doi.org/10.1007/s10620-021-07000-7
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author Ojima, Masahiro
Shimizu, Kentaro
Motooka, Daisuke
Ishihara, Takuma
Nakamura, Shota
Shintani, Ayumi
Ogura, Hiroshi
Iida, Tetsuya
Yoshiya, Kazuhisa
Shimazu, Takeshi
author_facet Ojima, Masahiro
Shimizu, Kentaro
Motooka, Daisuke
Ishihara, Takuma
Nakamura, Shota
Shintani, Ayumi
Ogura, Hiroshi
Iida, Tetsuya
Yoshiya, Kazuhisa
Shimazu, Takeshi
author_sort Ojima, Masahiro
collection PubMed
description BACKGROUND: The gut microbiota are reported to be altered in critical illness. The pattern and impact of dysbiosis on prognosis has not been thoroughly investigated in the ICU setting. AIMS: We aimed to evaluate changes in the gut microbiota of ICU patients via 16S rRNA gene deep sequencing, assess the association of the changes with antibiotics use or disease severity, and explore the association of gut microbiota changes with ICU patient prognosis. METHODS: Seventy-one mechanically ventilated patients were included. Fecal samples were collected serially on days 1–2, 3–4, 5–7, 8–14, and thereafter when suitable. Microorganisms of the fecal samples were profiled by 16S rRNA gene deep sequencing. RESULTS: Proportions of the five major phyla in the feces were diverse in each patient at admission. Those of Bacteroidetes and Firmicutes especially converged and stabilized within the first week from admission with a reduction in α-diversity (p < 0.001). Significant differences occurred in the proportional change of Actinobacteria between the carbapenem and non-carbapenem groups (p = 0.030) and that of Actinobacteria according to initial SOFA score and changes in the SOFA score (p < 0.001). An imbalance in the ratio of Bacteroidetes to Firmicutes within seven days from admission was associated with higher mortality when the ratio was > 8 or < 1/8 (odds ratio: 5.54, 95% CI: 1.39–22.18, p = 0.015). CONCLUSIONS: Broad-spectrum antibiotics and disease severity may be associated with gut dysbiosis in the ICU. A progression of dysbiosis occurring in the gut of ICU patients might be associated with mortality. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s10620-021-07000-7.
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spelling pubmed-80909182021-05-03 Gut Dysbiosis Associated with Antibiotics and Disease Severity and Its Relation to Mortality in Critically Ill Patients Ojima, Masahiro Shimizu, Kentaro Motooka, Daisuke Ishihara, Takuma Nakamura, Shota Shintani, Ayumi Ogura, Hiroshi Iida, Tetsuya Yoshiya, Kazuhisa Shimazu, Takeshi Dig Dis Sci Original Article BACKGROUND: The gut microbiota are reported to be altered in critical illness. The pattern and impact of dysbiosis on prognosis has not been thoroughly investigated in the ICU setting. AIMS: We aimed to evaluate changes in the gut microbiota of ICU patients via 16S rRNA gene deep sequencing, assess the association of the changes with antibiotics use or disease severity, and explore the association of gut microbiota changes with ICU patient prognosis. METHODS: Seventy-one mechanically ventilated patients were included. Fecal samples were collected serially on days 1–2, 3–4, 5–7, 8–14, and thereafter when suitable. Microorganisms of the fecal samples were profiled by 16S rRNA gene deep sequencing. RESULTS: Proportions of the five major phyla in the feces were diverse in each patient at admission. Those of Bacteroidetes and Firmicutes especially converged and stabilized within the first week from admission with a reduction in α-diversity (p < 0.001). Significant differences occurred in the proportional change of Actinobacteria between the carbapenem and non-carbapenem groups (p = 0.030) and that of Actinobacteria according to initial SOFA score and changes in the SOFA score (p < 0.001). An imbalance in the ratio of Bacteroidetes to Firmicutes within seven days from admission was associated with higher mortality when the ratio was > 8 or < 1/8 (odds ratio: 5.54, 95% CI: 1.39–22.18, p = 0.015). CONCLUSIONS: Broad-spectrum antibiotics and disease severity may be associated with gut dysbiosis in the ICU. A progression of dysbiosis occurring in the gut of ICU patients might be associated with mortality. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s10620-021-07000-7. Springer US 2021-05-03 2022 /pmc/articles/PMC8090918/ /pubmed/33939152 http://dx.doi.org/10.1007/s10620-021-07000-7 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by-nc/4.0/Open AccessThis article is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License, which permits any non-commercial 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-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) .
spellingShingle Original Article
Ojima, Masahiro
Shimizu, Kentaro
Motooka, Daisuke
Ishihara, Takuma
Nakamura, Shota
Shintani, Ayumi
Ogura, Hiroshi
Iida, Tetsuya
Yoshiya, Kazuhisa
Shimazu, Takeshi
Gut Dysbiosis Associated with Antibiotics and Disease Severity and Its Relation to Mortality in Critically Ill Patients
title Gut Dysbiosis Associated with Antibiotics and Disease Severity and Its Relation to Mortality in Critically Ill Patients
title_full Gut Dysbiosis Associated with Antibiotics and Disease Severity and Its Relation to Mortality in Critically Ill Patients
title_fullStr Gut Dysbiosis Associated with Antibiotics and Disease Severity and Its Relation to Mortality in Critically Ill Patients
title_full_unstemmed Gut Dysbiosis Associated with Antibiotics and Disease Severity and Its Relation to Mortality in Critically Ill Patients
title_short Gut Dysbiosis Associated with Antibiotics and Disease Severity and Its Relation to Mortality in Critically Ill Patients
title_sort gut dysbiosis associated with antibiotics and disease severity and its relation to mortality in critically ill patients
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8090918/
https://www.ncbi.nlm.nih.gov/pubmed/33939152
http://dx.doi.org/10.1007/s10620-021-07000-7
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