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Microbiome-associated human genetic variants impact phenome-wide disease risk

Human genetic variation associates with the composition of the gut microbiome, yet its influence on clinical traits remains largely unknown. We analyzed the consequences of nearly a thousand gut microbiome-associated variants (MAVs) on phenotypes reported in electronic health records from tens of th...

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Autores principales: Markowitz, Robert H. George, LaBella, Abigail Leavitt, Shi, Mingjian, Rokas, Antonis, Capra, John A., Ferguson, Jane F., Mosley, Jonathan D., Bordenstein, Seth R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: National Academy of Sciences 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9245617/
https://www.ncbi.nlm.nih.gov/pubmed/35749358
http://dx.doi.org/10.1073/pnas.2200551119
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author Markowitz, Robert H. George
LaBella, Abigail Leavitt
Shi, Mingjian
Rokas, Antonis
Capra, John A.
Ferguson, Jane F.
Mosley, Jonathan D.
Bordenstein, Seth R.
author_facet Markowitz, Robert H. George
LaBella, Abigail Leavitt
Shi, Mingjian
Rokas, Antonis
Capra, John A.
Ferguson, Jane F.
Mosley, Jonathan D.
Bordenstein, Seth R.
author_sort Markowitz, Robert H. George
collection PubMed
description Human genetic variation associates with the composition of the gut microbiome, yet its influence on clinical traits remains largely unknown. We analyzed the consequences of nearly a thousand gut microbiome-associated variants (MAVs) on phenotypes reported in electronic health records from tens of thousands of individuals. We discovered and replicated associations of MAVs with neurological, metabolic, digestive, and circulatory diseases. Five significant MAVs in these categories correlate with the relative abundance of microbes down to the strain level. We also demonstrate that these relationships are independently observed and concordant with microbe by disease associations reported in case–control studies. Moreover, a selective sweep and population differentiation impacted some disease-linked MAVs. Combined, these findings establish triad relationships among the human genome, microbiome, and disease. Consequently, human genetic influences may offer opportunities for precision diagnostics of microbiome-associated diseases but also highlight the relevance of genetic background for microbiome modulation and therapeutics.
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spelling pubmed-92456172022-12-24 Microbiome-associated human genetic variants impact phenome-wide disease risk Markowitz, Robert H. George LaBella, Abigail Leavitt Shi, Mingjian Rokas, Antonis Capra, John A. Ferguson, Jane F. Mosley, Jonathan D. Bordenstein, Seth R. Proc Natl Acad Sci U S A Biological Sciences Human genetic variation associates with the composition of the gut microbiome, yet its influence on clinical traits remains largely unknown. We analyzed the consequences of nearly a thousand gut microbiome-associated variants (MAVs) on phenotypes reported in electronic health records from tens of thousands of individuals. We discovered and replicated associations of MAVs with neurological, metabolic, digestive, and circulatory diseases. Five significant MAVs in these categories correlate with the relative abundance of microbes down to the strain level. We also demonstrate that these relationships are independently observed and concordant with microbe by disease associations reported in case–control studies. Moreover, a selective sweep and population differentiation impacted some disease-linked MAVs. Combined, these findings establish triad relationships among the human genome, microbiome, and disease. Consequently, human genetic influences may offer opportunities for precision diagnostics of microbiome-associated diseases but also highlight the relevance of genetic background for microbiome modulation and therapeutics. National Academy of Sciences 2022-06-24 2022-06-28 /pmc/articles/PMC9245617/ /pubmed/35749358 http://dx.doi.org/10.1073/pnas.2200551119 Text en Copyright © 2022 the Author(s). Published by PNAS. https://creativecommons.org/licenses/by-nc-nd/4.0/This article is distributed under Creative Commons Attribution-NonCommercial-NoDerivatives License 4.0 (CC BY-NC-ND) (https://creativecommons.org/licenses/by-nc-nd/4.0/) .
spellingShingle Biological Sciences
Markowitz, Robert H. George
LaBella, Abigail Leavitt
Shi, Mingjian
Rokas, Antonis
Capra, John A.
Ferguson, Jane F.
Mosley, Jonathan D.
Bordenstein, Seth R.
Microbiome-associated human genetic variants impact phenome-wide disease risk
title Microbiome-associated human genetic variants impact phenome-wide disease risk
title_full Microbiome-associated human genetic variants impact phenome-wide disease risk
title_fullStr Microbiome-associated human genetic variants impact phenome-wide disease risk
title_full_unstemmed Microbiome-associated human genetic variants impact phenome-wide disease risk
title_short Microbiome-associated human genetic variants impact phenome-wide disease risk
title_sort microbiome-associated human genetic variants impact phenome-wide disease risk
topic Biological Sciences
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9245617/
https://www.ncbi.nlm.nih.gov/pubmed/35749358
http://dx.doi.org/10.1073/pnas.2200551119
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