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Fecal microbiota transplantation for the treatment of irritable bowel syndrome: A systematic review and meta-analysis

BACKGROUND: Irritable bowel syndrome (IBS) is the most prevalent gastrointestinal disorder in developed countries and reduces patients’ quality of life, hinders their ability to work, and increases health care costs. A growing number of trials have demonstrated an aberrant gut microbiota composition...

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Autores principales: Halkjær, Sofie Ingdam, Lo, Bobby, Cold, Frederik, Højer Christensen, Alice, Holster, Savanne, König, Julia, Brummer, Robert Jan, Aroniadis, Olga C, Lahtinen, Perttu, Holvoet, Tom, Gluud, Lise Lotte, Petersen, Andreas Munk
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Baishideng Publishing Group Inc 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10280798/
https://www.ncbi.nlm.nih.gov/pubmed/37346153
http://dx.doi.org/10.3748/wjg.v29.i20.3185
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author Halkjær, Sofie Ingdam
Lo, Bobby
Cold, Frederik
Højer Christensen, Alice
Holster, Savanne
König, Julia
Brummer, Robert Jan
Aroniadis, Olga C
Lahtinen, Perttu
Holvoet, Tom
Gluud, Lise Lotte
Petersen, Andreas Munk
author_facet Halkjær, Sofie Ingdam
Lo, Bobby
Cold, Frederik
Højer Christensen, Alice
Holster, Savanne
König, Julia
Brummer, Robert Jan
Aroniadis, Olga C
Lahtinen, Perttu
Holvoet, Tom
Gluud, Lise Lotte
Petersen, Andreas Munk
author_sort Halkjær, Sofie Ingdam
collection PubMed
description BACKGROUND: Irritable bowel syndrome (IBS) is the most prevalent gastrointestinal disorder in developed countries and reduces patients’ quality of life, hinders their ability to work, and increases health care costs. A growing number of trials have demonstrated an aberrant gut microbiota composition in IBS, also known as ‘gut dysbiosis’. Fecal microbiota transplantation (FMT) has been suggested as a treatment for IBS. AIM: To assess the efficacy and safety of FMT for the treatment of IBS. METHODS: We searched Cochrane Central, MEDLINE, EMBASE and Web of Science up to 24 October 2022 for randomised controlled trials (RCTs) investigating the effectiveness of FMT compared to placebo (including autologous FMT) in treating IBS. The primary outcome was the number of patients with improvements of symptoms measured using a validated, global IBS symptoms score. Secondary outcomes were changes in quality-of-life scores, non-serious and serious adverse events. Risk ratios (RR) and corresponding 95%CI were calculated for dichotomous outcomes, as were the mean differences (MD) and 95%CI for continuous outcomes. The Cochrane risk of bias tool was used to assess the quality of the trials. GRADE criteria were used to assess the overall quality of the evidence. RESULTS: Eight RCTs (484 participants) were included in the review. FMT resulted in no significant benefit in IBS symptoms three months after treatment compared to placebo (RR 1.19, 95%CI: 0.68-2.10). Adverse events were reported in 97 participants in the FMT group and in 45 participants in the placebo group (RR 1.17, 95%CI: 0.63-2.15). One serious adverse event occurred in the FMT group and two in the placebo group (RR 0.42, 95%CI: 0.07-2.60). Endoscopic FMT delivery resulted in a significant improvement in symptoms, while capsules did not. FMT did not improve the quality of life of IBS patients but, instead, appeared to reduce it, albeit non significantly (MD -6.30, 95%CI: -13.39-0.79). The overall quality of the evidence was low due to moderate-high inconsistency, the small number of patients in the studies, and imprecision. CONCLUSION: We found insufficient evidence to support or refute the use of FMT for IBS. Larger trials are needed.
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spelling pubmed-102807982023-06-21 Fecal microbiota transplantation for the treatment of irritable bowel syndrome: A systematic review and meta-analysis Halkjær, Sofie Ingdam Lo, Bobby Cold, Frederik Højer Christensen, Alice Holster, Savanne König, Julia Brummer, Robert Jan Aroniadis, Olga C Lahtinen, Perttu Holvoet, Tom Gluud, Lise Lotte Petersen, Andreas Munk World J Gastroenterol Meta-Analysis BACKGROUND: Irritable bowel syndrome (IBS) is the most prevalent gastrointestinal disorder in developed countries and reduces patients’ quality of life, hinders their ability to work, and increases health care costs. A growing number of trials have demonstrated an aberrant gut microbiota composition in IBS, also known as ‘gut dysbiosis’. Fecal microbiota transplantation (FMT) has been suggested as a treatment for IBS. AIM: To assess the efficacy and safety of FMT for the treatment of IBS. METHODS: We searched Cochrane Central, MEDLINE, EMBASE and Web of Science up to 24 October 2022 for randomised controlled trials (RCTs) investigating the effectiveness of FMT compared to placebo (including autologous FMT) in treating IBS. The primary outcome was the number of patients with improvements of symptoms measured using a validated, global IBS symptoms score. Secondary outcomes were changes in quality-of-life scores, non-serious and serious adverse events. Risk ratios (RR) and corresponding 95%CI were calculated for dichotomous outcomes, as were the mean differences (MD) and 95%CI for continuous outcomes. The Cochrane risk of bias tool was used to assess the quality of the trials. GRADE criteria were used to assess the overall quality of the evidence. RESULTS: Eight RCTs (484 participants) were included in the review. FMT resulted in no significant benefit in IBS symptoms three months after treatment compared to placebo (RR 1.19, 95%CI: 0.68-2.10). Adverse events were reported in 97 participants in the FMT group and in 45 participants in the placebo group (RR 1.17, 95%CI: 0.63-2.15). One serious adverse event occurred in the FMT group and two in the placebo group (RR 0.42, 95%CI: 0.07-2.60). Endoscopic FMT delivery resulted in a significant improvement in symptoms, while capsules did not. FMT did not improve the quality of life of IBS patients but, instead, appeared to reduce it, albeit non significantly (MD -6.30, 95%CI: -13.39-0.79). The overall quality of the evidence was low due to moderate-high inconsistency, the small number of patients in the studies, and imprecision. CONCLUSION: We found insufficient evidence to support or refute the use of FMT for IBS. Larger trials are needed. Baishideng Publishing Group Inc 2023-05-28 2023-05-28 /pmc/articles/PMC10280798/ /pubmed/37346153 http://dx.doi.org/10.3748/wjg.v29.i20.3185 Text en ©The Author(s) 2023. 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.
spellingShingle Meta-Analysis
Halkjær, Sofie Ingdam
Lo, Bobby
Cold, Frederik
Højer Christensen, Alice
Holster, Savanne
König, Julia
Brummer, Robert Jan
Aroniadis, Olga C
Lahtinen, Perttu
Holvoet, Tom
Gluud, Lise Lotte
Petersen, Andreas Munk
Fecal microbiota transplantation for the treatment of irritable bowel syndrome: A systematic review and meta-analysis
title Fecal microbiota transplantation for the treatment of irritable bowel syndrome: A systematic review and meta-analysis
title_full Fecal microbiota transplantation for the treatment of irritable bowel syndrome: A systematic review and meta-analysis
title_fullStr Fecal microbiota transplantation for the treatment of irritable bowel syndrome: A systematic review and meta-analysis
title_full_unstemmed Fecal microbiota transplantation for the treatment of irritable bowel syndrome: A systematic review and meta-analysis
title_short Fecal microbiota transplantation for the treatment of irritable bowel syndrome: A systematic review and meta-analysis
title_sort fecal microbiota transplantation for the treatment of irritable bowel syndrome: a systematic review and meta-analysis
topic Meta-Analysis
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10280798/
https://www.ncbi.nlm.nih.gov/pubmed/37346153
http://dx.doi.org/10.3748/wjg.v29.i20.3185
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