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Saccharomyces cerevisiae I-3856 in irritable bowel syndrome with predominant constipation
BACKGROUND: Probiotics are a promising solution for managing irritable bowel syndrome (IBS). Saccharomyces cerevisiae (S. cerevisiae) I-3856 has already demonstrated beneficial effects in IBS subjects, particularly in IBS with predominant constipation (IBS-C). AIM: To confirm the efficacy of S. cere...
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/PMC9258277/ https://www.ncbi.nlm.nih.gov/pubmed/35979259 http://dx.doi.org/10.3748/wjg.v28.i22.2509 |
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author | Mourey, Florian Decherf, Amélie Jeanne, Jean-François Clément-Ziza, Mathieu Grisoni, Marie-Lise Machuron, François Legrain-Raspaud, Sophie Bourreille, Arnaud Desreumaux, Pierre |
author_facet | Mourey, Florian Decherf, Amélie Jeanne, Jean-François Clément-Ziza, Mathieu Grisoni, Marie-Lise Machuron, François Legrain-Raspaud, Sophie Bourreille, Arnaud Desreumaux, Pierre |
author_sort | Mourey, Florian |
collection | PubMed |
description | BACKGROUND: Probiotics are a promising solution for managing irritable bowel syndrome (IBS). Saccharomyces cerevisiae (S. cerevisiae) I-3856 has already demonstrated beneficial effects in IBS subjects, particularly in IBS with predominant constipation (IBS-C). AIM: To confirm the efficacy of S. cerevisiae I-3856 in the management of gastrointestinal symptoms in IBS-C. METHODS: A randomized, double-blind, placebo-controlled clinical study was performed in a total of 456 subjects. After a run-in period, subjects were randomly assigned to the group receiving S. cerevisiae I-3856 (8 × 10(9 )CFU daily) or the placebo for 8 wk, and they performed daily self-evaluations of gastrointestinal symptoms. The primary objective was to assess the effect of the probiotic on abdominal pain. The secondary objectives were the evaluation of other gastrointestinal symptoms, bowel movement frequency and consistency, and quality of life (QOL). RESULTS: A significantly higher proportion of abdominal pain responders was reported in the Probiotic group (45.1% vs 33.9%, P = 0.017). A nonsignificant difference in the area under the curve for abdominal pain over the second month of supplementation was observed in subjects receiving probiotic vs placebo [P = 0.073, 95%CI: -0.59 (-1.23; 0.05)]. No statistically significant differences were reported in the evolution of bowel movement frequency and stool consistency between the groups. After 8 wk of supplementation, the overall QOL score was significantly higher in the Probiotic group than in the Placebo group [P = 0.047, 95%CI: 3.86 (0.52; 7.20)]. Furthermore, exploratory analyses showed statistically significant and clinically relevant improvements in QOL scores in abdominal pain responders vs nonresponders. CONCLUSION: The results of this clinical study confirmed the abdominal pain alleviation properties of S. cerevisiae I-3856 in IBS-C. Abdominal pain relief was associated with improved QOL. ClinicalTrials.gov identifier: NCT03150212. |
format | Online Article Text |
id | pubmed-9258277 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Baishideng Publishing Group Inc |
record_format | MEDLINE/PubMed |
spelling | pubmed-92582772022-08-16 Saccharomyces cerevisiae I-3856 in irritable bowel syndrome with predominant constipation Mourey, Florian Decherf, Amélie Jeanne, Jean-François Clément-Ziza, Mathieu Grisoni, Marie-Lise Machuron, François Legrain-Raspaud, Sophie Bourreille, Arnaud Desreumaux, Pierre World J Gastroenterol Randomized Controlled Trial BACKGROUND: Probiotics are a promising solution for managing irritable bowel syndrome (IBS). Saccharomyces cerevisiae (S. cerevisiae) I-3856 has already demonstrated beneficial effects in IBS subjects, particularly in IBS with predominant constipation (IBS-C). AIM: To confirm the efficacy of S. cerevisiae I-3856 in the management of gastrointestinal symptoms in IBS-C. METHODS: A randomized, double-blind, placebo-controlled clinical study was performed in a total of 456 subjects. After a run-in period, subjects were randomly assigned to the group receiving S. cerevisiae I-3856 (8 × 10(9 )CFU daily) or the placebo for 8 wk, and they performed daily self-evaluations of gastrointestinal symptoms. The primary objective was to assess the effect of the probiotic on abdominal pain. The secondary objectives were the evaluation of other gastrointestinal symptoms, bowel movement frequency and consistency, and quality of life (QOL). RESULTS: A significantly higher proportion of abdominal pain responders was reported in the Probiotic group (45.1% vs 33.9%, P = 0.017). A nonsignificant difference in the area under the curve for abdominal pain over the second month of supplementation was observed in subjects receiving probiotic vs placebo [P = 0.073, 95%CI: -0.59 (-1.23; 0.05)]. No statistically significant differences were reported in the evolution of bowel movement frequency and stool consistency between the groups. After 8 wk of supplementation, the overall QOL score was significantly higher in the Probiotic group than in the Placebo group [P = 0.047, 95%CI: 3.86 (0.52; 7.20)]. Furthermore, exploratory analyses showed statistically significant and clinically relevant improvements in QOL scores in abdominal pain responders vs nonresponders. CONCLUSION: The results of this clinical study confirmed the abdominal pain alleviation properties of S. cerevisiae I-3856 in IBS-C. Abdominal pain relief was associated with improved QOL. ClinicalTrials.gov identifier: NCT03150212. Baishideng Publishing Group Inc 2022-06-14 2022-06-14 /pmc/articles/PMC9258277/ /pubmed/35979259 http://dx.doi.org/10.3748/wjg.v28.i22.2509 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 | Randomized Controlled Trial Mourey, Florian Decherf, Amélie Jeanne, Jean-François Clément-Ziza, Mathieu Grisoni, Marie-Lise Machuron, François Legrain-Raspaud, Sophie Bourreille, Arnaud Desreumaux, Pierre Saccharomyces cerevisiae I-3856 in irritable bowel syndrome with predominant constipation |
title |
Saccharomyces cerevisiae I-3856 in irritable bowel syndrome with predominant constipation |
title_full |
Saccharomyces cerevisiae I-3856 in irritable bowel syndrome with predominant constipation |
title_fullStr |
Saccharomyces cerevisiae I-3856 in irritable bowel syndrome with predominant constipation |
title_full_unstemmed |
Saccharomyces cerevisiae I-3856 in irritable bowel syndrome with predominant constipation |
title_short |
Saccharomyces cerevisiae I-3856 in irritable bowel syndrome with predominant constipation |
title_sort | saccharomyces cerevisiae i-3856 in irritable bowel syndrome with predominant constipation |
topic | Randomized Controlled Trial |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9258277/ https://www.ncbi.nlm.nih.gov/pubmed/35979259 http://dx.doi.org/10.3748/wjg.v28.i22.2509 |
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