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Gut bacterial microbiome composition and statin intake—A systematic review

Recently, the gut microbiome has become an important field of interest. Indeed, the microbiome has been associated to numerous drug interactions and it is thought to influence the efficacy of pharmacologic treatments. Although statins are widely prescribed medications, there remains considerable var...

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Autores principales: Dias, Andreia M., Cordeiro, Gonçalo, Estevinho, Maria M., Veiga, Rui, Figueira, Luis, Reina‐Couto, Marta, Magro, Fernando
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7261966/
https://www.ncbi.nlm.nih.gov/pubmed/32476298
http://dx.doi.org/10.1002/prp2.601
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author Dias, Andreia M.
Cordeiro, Gonçalo
Estevinho, Maria M.
Veiga, Rui
Figueira, Luis
Reina‐Couto, Marta
Magro, Fernando
author_facet Dias, Andreia M.
Cordeiro, Gonçalo
Estevinho, Maria M.
Veiga, Rui
Figueira, Luis
Reina‐Couto, Marta
Magro, Fernando
author_sort Dias, Andreia M.
collection PubMed
description Recently, the gut microbiome has become an important field of interest. Indeed, the microbiome has been associated to numerous drug interactions and it is thought to influence the efficacy of pharmacologic treatments. Although statins are widely prescribed medications, there remains considerable variability in its therapeutic response. In this context, we aimed to investigate how statins modulate the gut microbiome and, reversely, how can the microbiome influence the course of anti‐hypercholesterolemic treatment. We conducted a systematic review by searching four online databases, in accordance with PRISMA guidelines. Studies addressing gut microbiome changes following statin treatment and those assessing statins’ response and associating it with patients’ microbiome were included. Due to the limited number of results, we decided to include studies enrolling both humans and animals. We summarized information from three human and seven animal studies and aimed to assess the influence of gut microbiome composition on statin response (Outcome 1) and to evaluate the impact of statin treatment on the gut microbiome (Outcome 2). An association between a certain microbiome composition that promoted the lipid‐lowering effect of statins was found. However, what kind of microorganisms and how they can exert this effect remains uncertain. Furthermore, statins might have a role in the modulation of the gut microbiome, but then again, it is still unknown whether this change is directly caused by the drug or another metabolic mechanism. Even though gut microbiota may have several potential therapeutic implications, its use as a personalized predictive biomarker requires further studies.
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spelling pubmed-72619662020-06-01 Gut bacterial microbiome composition and statin intake—A systematic review Dias, Andreia M. Cordeiro, Gonçalo Estevinho, Maria M. Veiga, Rui Figueira, Luis Reina‐Couto, Marta Magro, Fernando Pharmacol Res Perspect Reviews Recently, the gut microbiome has become an important field of interest. Indeed, the microbiome has been associated to numerous drug interactions and it is thought to influence the efficacy of pharmacologic treatments. Although statins are widely prescribed medications, there remains considerable variability in its therapeutic response. In this context, we aimed to investigate how statins modulate the gut microbiome and, reversely, how can the microbiome influence the course of anti‐hypercholesterolemic treatment. We conducted a systematic review by searching four online databases, in accordance with PRISMA guidelines. Studies addressing gut microbiome changes following statin treatment and those assessing statins’ response and associating it with patients’ microbiome were included. Due to the limited number of results, we decided to include studies enrolling both humans and animals. We summarized information from three human and seven animal studies and aimed to assess the influence of gut microbiome composition on statin response (Outcome 1) and to evaluate the impact of statin treatment on the gut microbiome (Outcome 2). An association between a certain microbiome composition that promoted the lipid‐lowering effect of statins was found. However, what kind of microorganisms and how they can exert this effect remains uncertain. Furthermore, statins might have a role in the modulation of the gut microbiome, but then again, it is still unknown whether this change is directly caused by the drug or another metabolic mechanism. Even though gut microbiota may have several potential therapeutic implications, its use as a personalized predictive biomarker requires further studies. John Wiley and Sons Inc. 2020-05-31 /pmc/articles/PMC7261966/ /pubmed/32476298 http://dx.doi.org/10.1002/prp2.601 Text en © 2020 The Authors. Pharmacology Research & Perspectives published by John Wiley & Sons Ltd, British Pharmacological Society and American Society for Pharmacology and Experimental Therapeutics. This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Reviews
Dias, Andreia M.
Cordeiro, Gonçalo
Estevinho, Maria M.
Veiga, Rui
Figueira, Luis
Reina‐Couto, Marta
Magro, Fernando
Gut bacterial microbiome composition and statin intake—A systematic review
title Gut bacterial microbiome composition and statin intake—A systematic review
title_full Gut bacterial microbiome composition and statin intake—A systematic review
title_fullStr Gut bacterial microbiome composition and statin intake—A systematic review
title_full_unstemmed Gut bacterial microbiome composition and statin intake—A systematic review
title_short Gut bacterial microbiome composition and statin intake—A systematic review
title_sort gut bacterial microbiome composition and statin intake—a systematic review
topic Reviews
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7261966/
https://www.ncbi.nlm.nih.gov/pubmed/32476298
http://dx.doi.org/10.1002/prp2.601
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