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Distal Gastrectomy with Billroth II Reconstruction is Associated with Oralization of Gut Microbiome and Intestinal Inflammation: A Proof-of-Concept Study

BACKGROUND: Subtotal gastrectomy with Billroth II reconstruction (SGB2) results in increased gastric pH and diminished gastric barrier. Increased gastric pH following PPI therapy has an impact on the gut microbiome, intestinal inflammation, and possibly patient health. If similar changes are present...

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Autores principales: Horvath, Angela, Bausys, Augustinas, Sabaliauskaite, Rasa, Stratilatovas, Eugenijus, Jarmalaite, Sonata, Schuetz, Burkhard, Stiegler, Philipp, Bausys, Rimantas, Stadlbauer, Vanessa, Strupas, Kestutis
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer International Publishing 2020
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Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7801296/
https://www.ncbi.nlm.nih.gov/pubmed/32504369
http://dx.doi.org/10.1245/s10434-020-08678-1
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author Horvath, Angela
Bausys, Augustinas
Sabaliauskaite, Rasa
Stratilatovas, Eugenijus
Jarmalaite, Sonata
Schuetz, Burkhard
Stiegler, Philipp
Bausys, Rimantas
Stadlbauer, Vanessa
Strupas, Kestutis
author_facet Horvath, Angela
Bausys, Augustinas
Sabaliauskaite, Rasa
Stratilatovas, Eugenijus
Jarmalaite, Sonata
Schuetz, Burkhard
Stiegler, Philipp
Bausys, Rimantas
Stadlbauer, Vanessa
Strupas, Kestutis
author_sort Horvath, Angela
collection PubMed
description BACKGROUND: Subtotal gastrectomy with Billroth II reconstruction (SGB2) results in increased gastric pH and diminished gastric barrier. Increased gastric pH following PPI therapy has an impact on the gut microbiome, intestinal inflammation, and possibly patient health. If similar changes are present after SGB2, these can be relevant for patient health and long-term outcomes after surgery. The aim of the study is to investigate whether SGB2 is associated with specific changes in gut microbiome composition and intestinal inflammation. PATIENTS AND METHODS: This cross-sectional proof-of-concept study includes patients after SGB2 (n = 14) for early gastric cancer and their nongastrectomized in-house relatives as controls (n = 8). Fecal microbiome composition, intestinal inflammation (fecal calprotectin), gut permeability (DAO, LBP, sCD14), systemic inflammation (CRP) markers, and gastrointestinal symptoms are investigated. This study is registered at ClinicalTrials.gov (NCT03418428). RESULTS: Microbiome oralization following SGB2 was defined by an increase in Escherichia–Shigella, Enterococcus, Streptococcus, and other typical oral cavity bacteria (Veillonella, Oribacterium, and Mogibacterium) abundance. The fecal calprotectin was increased in the SGB2 group [100.9 (52.1; 292) vs. 25.8 (17; 66.5); p = 0.014], and calprotectin levels positively correlated with the abundance of Streptococcus (r(s) = 0.639; p(adj) = 0.023). Gastrointestinal symptoms in SGB2 patients were associated with distinct taxonomic changes of the gut microbiome. CONCLUSIONS: SGB2 is associated with oralization of the gut microbiome; intestinal inflammation and microbiome changes were associated with gastrointestinal symptoms. These novel findings may open gut microbiome as a new target for therapy to improve quality of life and general patient health in long-term survivors after SGB2.
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spelling pubmed-78012962021-01-21 Distal Gastrectomy with Billroth II Reconstruction is Associated with Oralization of Gut Microbiome and Intestinal Inflammation: A Proof-of-Concept Study Horvath, Angela Bausys, Augustinas Sabaliauskaite, Rasa Stratilatovas, Eugenijus Jarmalaite, Sonata Schuetz, Burkhard Stiegler, Philipp Bausys, Rimantas Stadlbauer, Vanessa Strupas, Kestutis Ann Surg Oncol Translational Research and Biomarkers BACKGROUND: Subtotal gastrectomy with Billroth II reconstruction (SGB2) results in increased gastric pH and diminished gastric barrier. Increased gastric pH following PPI therapy has an impact on the gut microbiome, intestinal inflammation, and possibly patient health. If similar changes are present after SGB2, these can be relevant for patient health and long-term outcomes after surgery. The aim of the study is to investigate whether SGB2 is associated with specific changes in gut microbiome composition and intestinal inflammation. PATIENTS AND METHODS: This cross-sectional proof-of-concept study includes patients after SGB2 (n = 14) for early gastric cancer and their nongastrectomized in-house relatives as controls (n = 8). Fecal microbiome composition, intestinal inflammation (fecal calprotectin), gut permeability (DAO, LBP, sCD14), systemic inflammation (CRP) markers, and gastrointestinal symptoms are investigated. This study is registered at ClinicalTrials.gov (NCT03418428). RESULTS: Microbiome oralization following SGB2 was defined by an increase in Escherichia–Shigella, Enterococcus, Streptococcus, and other typical oral cavity bacteria (Veillonella, Oribacterium, and Mogibacterium) abundance. The fecal calprotectin was increased in the SGB2 group [100.9 (52.1; 292) vs. 25.8 (17; 66.5); p = 0.014], and calprotectin levels positively correlated with the abundance of Streptococcus (r(s) = 0.639; p(adj) = 0.023). Gastrointestinal symptoms in SGB2 patients were associated with distinct taxonomic changes of the gut microbiome. CONCLUSIONS: SGB2 is associated with oralization of the gut microbiome; intestinal inflammation and microbiome changes were associated with gastrointestinal symptoms. These novel findings may open gut microbiome as a new target for therapy to improve quality of life and general patient health in long-term survivors after SGB2. Springer International Publishing 2020-06-05 2021 /pmc/articles/PMC7801296/ /pubmed/32504369 http://dx.doi.org/10.1245/s10434-020-08678-1 Text en © The Author(s) 2020 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/.
spellingShingle Translational Research and Biomarkers
Horvath, Angela
Bausys, Augustinas
Sabaliauskaite, Rasa
Stratilatovas, Eugenijus
Jarmalaite, Sonata
Schuetz, Burkhard
Stiegler, Philipp
Bausys, Rimantas
Stadlbauer, Vanessa
Strupas, Kestutis
Distal Gastrectomy with Billroth II Reconstruction is Associated with Oralization of Gut Microbiome and Intestinal Inflammation: A Proof-of-Concept Study
title Distal Gastrectomy with Billroth II Reconstruction is Associated with Oralization of Gut Microbiome and Intestinal Inflammation: A Proof-of-Concept Study
title_full Distal Gastrectomy with Billroth II Reconstruction is Associated with Oralization of Gut Microbiome and Intestinal Inflammation: A Proof-of-Concept Study
title_fullStr Distal Gastrectomy with Billroth II Reconstruction is Associated with Oralization of Gut Microbiome and Intestinal Inflammation: A Proof-of-Concept Study
title_full_unstemmed Distal Gastrectomy with Billroth II Reconstruction is Associated with Oralization of Gut Microbiome and Intestinal Inflammation: A Proof-of-Concept Study
title_short Distal Gastrectomy with Billroth II Reconstruction is Associated with Oralization of Gut Microbiome and Intestinal Inflammation: A Proof-of-Concept Study
title_sort distal gastrectomy with billroth ii reconstruction is associated with oralization of gut microbiome and intestinal inflammation: a proof-of-concept study
topic Translational Research and Biomarkers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7801296/
https://www.ncbi.nlm.nih.gov/pubmed/32504369
http://dx.doi.org/10.1245/s10434-020-08678-1
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