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Impact of commonly used drugs on the composition and metabolic function of the gut microbiota

The human gut microbiota has now been associated with drug responses and efficacy, while chemical compounds present in these drugs can also impact the gut bacteria. However, drug–microbe interactions are still understudied in the clinical context, where polypharmacy and comorbidities co-occur. Here,...

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Autores principales: Vich Vila, Arnau, Collij, Valerie, Sanna, Serena, Sinha, Trishla, Imhann, Floris, Bourgonje, Arno R., Mujagic, Zlatan, Jonkers, Daisy M. A. E., Masclee, Ad A. M., Fu, Jingyuan, Kurilshikov, Alexander, Wijmenga, Cisca, Zhernakova, Alexandra, Weersma, Rinse K.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6969170/
https://www.ncbi.nlm.nih.gov/pubmed/31953381
http://dx.doi.org/10.1038/s41467-019-14177-z
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author Vich Vila, Arnau
Collij, Valerie
Sanna, Serena
Sinha, Trishla
Imhann, Floris
Bourgonje, Arno R.
Mujagic, Zlatan
Jonkers, Daisy M. A. E.
Masclee, Ad A. M.
Fu, Jingyuan
Kurilshikov, Alexander
Wijmenga, Cisca
Zhernakova, Alexandra
Weersma, Rinse K.
author_facet Vich Vila, Arnau
Collij, Valerie
Sanna, Serena
Sinha, Trishla
Imhann, Floris
Bourgonje, Arno R.
Mujagic, Zlatan
Jonkers, Daisy M. A. E.
Masclee, Ad A. M.
Fu, Jingyuan
Kurilshikov, Alexander
Wijmenga, Cisca
Zhernakova, Alexandra
Weersma, Rinse K.
author_sort Vich Vila, Arnau
collection PubMed
description The human gut microbiota has now been associated with drug responses and efficacy, while chemical compounds present in these drugs can also impact the gut bacteria. However, drug–microbe interactions are still understudied in the clinical context, where polypharmacy and comorbidities co-occur. Here, we report relations between commonly used drugs and the gut microbiome. We performed metagenomics sequencing of faecal samples from a population cohort and two gastrointestinal disease cohorts. Differences between users and non-users were analysed per cohort, followed by a meta-analysis. While 19 of 41 drugs are found to be associated with microbial features, when controlling for the use of multiple medications, proton-pump inhibitors, metformin, antibiotics and laxatives show the strongest associations with the microbiome. We here provide evidence for extensive changes in taxonomy, metabolic potential and resistome in relation to commonly used drugs. This paves the way for future studies and has implications for current microbiome studies by demonstrating the need to correct for multiple drug use.
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spelling pubmed-69691702020-01-21 Impact of commonly used drugs on the composition and metabolic function of the gut microbiota Vich Vila, Arnau Collij, Valerie Sanna, Serena Sinha, Trishla Imhann, Floris Bourgonje, Arno R. Mujagic, Zlatan Jonkers, Daisy M. A. E. Masclee, Ad A. M. Fu, Jingyuan Kurilshikov, Alexander Wijmenga, Cisca Zhernakova, Alexandra Weersma, Rinse K. Nat Commun Article The human gut microbiota has now been associated with drug responses and efficacy, while chemical compounds present in these drugs can also impact the gut bacteria. However, drug–microbe interactions are still understudied in the clinical context, where polypharmacy and comorbidities co-occur. Here, we report relations between commonly used drugs and the gut microbiome. We performed metagenomics sequencing of faecal samples from a population cohort and two gastrointestinal disease cohorts. Differences between users and non-users were analysed per cohort, followed by a meta-analysis. While 19 of 41 drugs are found to be associated with microbial features, when controlling for the use of multiple medications, proton-pump inhibitors, metformin, antibiotics and laxatives show the strongest associations with the microbiome. We here provide evidence for extensive changes in taxonomy, metabolic potential and resistome in relation to commonly used drugs. This paves the way for future studies and has implications for current microbiome studies by demonstrating the need to correct for multiple drug use. Nature Publishing Group UK 2020-01-17 /pmc/articles/PMC6969170/ /pubmed/31953381 http://dx.doi.org/10.1038/s41467-019-14177-z 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Vich Vila, Arnau
Collij, Valerie
Sanna, Serena
Sinha, Trishla
Imhann, Floris
Bourgonje, Arno R.
Mujagic, Zlatan
Jonkers, Daisy M. A. E.
Masclee, Ad A. M.
Fu, Jingyuan
Kurilshikov, Alexander
Wijmenga, Cisca
Zhernakova, Alexandra
Weersma, Rinse K.
Impact of commonly used drugs on the composition and metabolic function of the gut microbiota
title Impact of commonly used drugs on the composition and metabolic function of the gut microbiota
title_full Impact of commonly used drugs on the composition and metabolic function of the gut microbiota
title_fullStr Impact of commonly used drugs on the composition and metabolic function of the gut microbiota
title_full_unstemmed Impact of commonly used drugs on the composition and metabolic function of the gut microbiota
title_short Impact of commonly used drugs on the composition and metabolic function of the gut microbiota
title_sort impact of commonly used drugs on the composition and metabolic function of the gut microbiota
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6969170/
https://www.ncbi.nlm.nih.gov/pubmed/31953381
http://dx.doi.org/10.1038/s41467-019-14177-z
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