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Association between antibiotics and gut microbiome dysbiosis in children: systematic review and meta-analysis

Antibiotics in childhood have been linked with diseases including asthma, juvenile arthritis, type 1 diabetes, Crohn’s disease and mental illness. The underlying mechanisms are thought related to dysbiosis of the gut microbiome. We conducted a systematic review of the association between antibiotics...

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Autores principales: McDonnell, Lucy, Gilkes, Alexander, Ashworth, Mark, Rowland, Victoria, Harries, Timothy Hugh, Armstrong, David, White, Patrick
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7928022/
https://www.ncbi.nlm.nih.gov/pubmed/33651651
http://dx.doi.org/10.1080/19490976.2020.1870402
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author McDonnell, Lucy
Gilkes, Alexander
Ashworth, Mark
Rowland, Victoria
Harries, Timothy Hugh
Armstrong, David
White, Patrick
author_facet McDonnell, Lucy
Gilkes, Alexander
Ashworth, Mark
Rowland, Victoria
Harries, Timothy Hugh
Armstrong, David
White, Patrick
author_sort McDonnell, Lucy
collection PubMed
description Antibiotics in childhood have been linked with diseases including asthma, juvenile arthritis, type 1 diabetes, Crohn’s disease and mental illness. The underlying mechanisms are thought related to dysbiosis of the gut microbiome. We conducted a systematic review of the association between antibiotics and disruption of the pediatric gut microbiome. Searches used MEDLINE, EMBASE and Web of Science. Eligible studies: association between antibiotics and gut microbiome dysbiosis; children 0–18 years; molecular techniques of assessment; outcomes of microbiome richness, diversity or composition. Quality assessed by Newcastle–Ottawa Scale or Cochrane Risk of Bias Tool. Meta-analysis where possible. A total of 4,668 publications identified: 12 in final analysis (5 randomized controlled trials (RCTs), 5 cohort studies, 2 cross-sectional studies). Microbiome richness was measured in 3 studies, species diversity in 6, and species composition in 10. Quality of evidence was good or fair. 5 studies found a significant reduction in diversity and 3 a significant reduction in richness. Macrolide exposure was associated with reduced richness for twice as long as penicillin. Significant reductions were seen in Bifidobacteria (5 studies) and Lactobacillus (2 studies), and significant increases in Proteobacteria such as E. coli (4 studies). A meta-analysis of RCTs of the effect of macrolide (azithromycin) exposure on the gut microbiome found a significant reduction in alpha-diversity (Shannon index: mean difference −0.86 (95% CI −1.59, −0.13). Antibiotic exposure was associated with reduced microbiome diversity and richness, and with changes in bacterial abundance. The potential for dysbiosis in the microbiome should be taken into account when prescribing antibiotics for children. Systematic review registration number: CRD42018094188
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spelling pubmed-79280222021-03-05 Association between antibiotics and gut microbiome dysbiosis in children: systematic review and meta-analysis McDonnell, Lucy Gilkes, Alexander Ashworth, Mark Rowland, Victoria Harries, Timothy Hugh Armstrong, David White, Patrick Gut Microbes Research Paper Antibiotics in childhood have been linked with diseases including asthma, juvenile arthritis, type 1 diabetes, Crohn’s disease and mental illness. The underlying mechanisms are thought related to dysbiosis of the gut microbiome. We conducted a systematic review of the association between antibiotics and disruption of the pediatric gut microbiome. Searches used MEDLINE, EMBASE and Web of Science. Eligible studies: association between antibiotics and gut microbiome dysbiosis; children 0–18 years; molecular techniques of assessment; outcomes of microbiome richness, diversity or composition. Quality assessed by Newcastle–Ottawa Scale or Cochrane Risk of Bias Tool. Meta-analysis where possible. A total of 4,668 publications identified: 12 in final analysis (5 randomized controlled trials (RCTs), 5 cohort studies, 2 cross-sectional studies). Microbiome richness was measured in 3 studies, species diversity in 6, and species composition in 10. Quality of evidence was good or fair. 5 studies found a significant reduction in diversity and 3 a significant reduction in richness. Macrolide exposure was associated with reduced richness for twice as long as penicillin. Significant reductions were seen in Bifidobacteria (5 studies) and Lactobacillus (2 studies), and significant increases in Proteobacteria such as E. coli (4 studies). A meta-analysis of RCTs of the effect of macrolide (azithromycin) exposure on the gut microbiome found a significant reduction in alpha-diversity (Shannon index: mean difference −0.86 (95% CI −1.59, −0.13). Antibiotic exposure was associated with reduced microbiome diversity and richness, and with changes in bacterial abundance. The potential for dysbiosis in the microbiome should be taken into account when prescribing antibiotics for children. Systematic review registration number: CRD42018094188 Taylor & Francis 2021-03-02 /pmc/articles/PMC7928022/ /pubmed/33651651 http://dx.doi.org/10.1080/19490976.2020.1870402 Text en © 2021 The Author(s). Published with license by Taylor & Francis Group, LLC. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Paper
McDonnell, Lucy
Gilkes, Alexander
Ashworth, Mark
Rowland, Victoria
Harries, Timothy Hugh
Armstrong, David
White, Patrick
Association between antibiotics and gut microbiome dysbiosis in children: systematic review and meta-analysis
title Association between antibiotics and gut microbiome dysbiosis in children: systematic review and meta-analysis
title_full Association between antibiotics and gut microbiome dysbiosis in children: systematic review and meta-analysis
title_fullStr Association between antibiotics and gut microbiome dysbiosis in children: systematic review and meta-analysis
title_full_unstemmed Association between antibiotics and gut microbiome dysbiosis in children: systematic review and meta-analysis
title_short Association between antibiotics and gut microbiome dysbiosis in children: systematic review and meta-analysis
title_sort association between antibiotics and gut microbiome dysbiosis in children: systematic review and meta-analysis
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7928022/
https://www.ncbi.nlm.nih.gov/pubmed/33651651
http://dx.doi.org/10.1080/19490976.2020.1870402
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