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Antibiotic use and risk of colorectal cancer: a systematic review and dose–response meta-analysis

BACKGROUND: It is understudied whether the posed association of oral antibiotics with colorectal cancer (CRC) varies between antibiotic spectrums, colorectal continuum, and if a non-linear dose-dependent relationship is present. DESIGN: Three electronic databases and a trial platform were searched f...

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Autores principales: Simin, Johanna, Fornes, Romina, Liu, Qing, Olsen, Renate Slind, Callens, Steven, Engstrand, Lars, Brusselaers, Nele
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7722751/
https://www.ncbi.nlm.nih.gov/pubmed/32968205
http://dx.doi.org/10.1038/s41416-020-01082-2
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author Simin, Johanna
Fornes, Romina
Liu, Qing
Olsen, Renate Slind
Callens, Steven
Engstrand, Lars
Brusselaers, Nele
author_facet Simin, Johanna
Fornes, Romina
Liu, Qing
Olsen, Renate Slind
Callens, Steven
Engstrand, Lars
Brusselaers, Nele
author_sort Simin, Johanna
collection PubMed
description BACKGROUND: It is understudied whether the posed association of oral antibiotics with colorectal cancer (CRC) varies between antibiotic spectrums, colorectal continuum, and if a non-linear dose-dependent relationship is present. DESIGN: Three electronic databases and a trial platform were searched for all relevant studies, from inception until February 2020, without restrictions. Random-effects meta-analyses provided pooled effect-sizes (ES) with 95% confidence intervals (CI). Dose–response analyses modelling the relationship between number of days exposed to antibiotics and CRC risk were extended to non-linear multivariable random-effects models. RESULTS: Of 6483 identified publications ten were eligible, including 4.1 million individuals and over 73,550 CRC cases. The pooled CRC risk was increased among individuals who ever-used antibiotics (ES = 1.17, 95%CI 1.05–1.30), particularly for broad-spectrum antibiotics (ES = 1.70, 95%CI 1.26–2.30), but not for narrow-spectrum antibiotic (ES = 1.11, 95% 0.93–1.32). The dose–response analysis did not provide strong evidence of any particular dose–response association, and the risk patterns were rather similar for colon and rectal cancer. DISCUSSION: The antibiotic use associated CRC risk seemingly differs between broad- and narrow-spectrum antibiotics, and possibly within the colorectal continuum. It remains unclear whether this association is causal, requiring more mechanistic studies and further clarification of drug–microbiome interactions.
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spelling pubmed-77227512021-09-24 Antibiotic use and risk of colorectal cancer: a systematic review and dose–response meta-analysis Simin, Johanna Fornes, Romina Liu, Qing Olsen, Renate Slind Callens, Steven Engstrand, Lars Brusselaers, Nele Br J Cancer Article BACKGROUND: It is understudied whether the posed association of oral antibiotics with colorectal cancer (CRC) varies between antibiotic spectrums, colorectal continuum, and if a non-linear dose-dependent relationship is present. DESIGN: Three electronic databases and a trial platform were searched for all relevant studies, from inception until February 2020, without restrictions. Random-effects meta-analyses provided pooled effect-sizes (ES) with 95% confidence intervals (CI). Dose–response analyses modelling the relationship between number of days exposed to antibiotics and CRC risk were extended to non-linear multivariable random-effects models. RESULTS: Of 6483 identified publications ten were eligible, including 4.1 million individuals and over 73,550 CRC cases. The pooled CRC risk was increased among individuals who ever-used antibiotics (ES = 1.17, 95%CI 1.05–1.30), particularly for broad-spectrum antibiotics (ES = 1.70, 95%CI 1.26–2.30), but not for narrow-spectrum antibiotic (ES = 1.11, 95% 0.93–1.32). The dose–response analysis did not provide strong evidence of any particular dose–response association, and the risk patterns were rather similar for colon and rectal cancer. DISCUSSION: The antibiotic use associated CRC risk seemingly differs between broad- and narrow-spectrum antibiotics, and possibly within the colorectal continuum. It remains unclear whether this association is causal, requiring more mechanistic studies and further clarification of drug–microbiome interactions. Nature Publishing Group UK 2020-09-24 2020-12-08 /pmc/articles/PMC7722751/ /pubmed/32968205 http://dx.doi.org/10.1038/s41416-020-01082-2 Text en © The Author(s), under exclusive licence to Cancer Research UK 2020 https://creativecommons.org/licenses/by/4.0/Note This work is published under the standard license to publish agreement. After 12 months the work will become freely available and the license terms will switch to a Creative Commons Attribution 4.0 International (CC BY 4.0).
spellingShingle Article
Simin, Johanna
Fornes, Romina
Liu, Qing
Olsen, Renate Slind
Callens, Steven
Engstrand, Lars
Brusselaers, Nele
Antibiotic use and risk of colorectal cancer: a systematic review and dose–response meta-analysis
title Antibiotic use and risk of colorectal cancer: a systematic review and dose–response meta-analysis
title_full Antibiotic use and risk of colorectal cancer: a systematic review and dose–response meta-analysis
title_fullStr Antibiotic use and risk of colorectal cancer: a systematic review and dose–response meta-analysis
title_full_unstemmed Antibiotic use and risk of colorectal cancer: a systematic review and dose–response meta-analysis
title_short Antibiotic use and risk of colorectal cancer: a systematic review and dose–response meta-analysis
title_sort antibiotic use and risk of colorectal cancer: a systematic review and dose–response meta-analysis
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7722751/
https://www.ncbi.nlm.nih.gov/pubmed/32968205
http://dx.doi.org/10.1038/s41416-020-01082-2
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