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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...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
National Academy of Sciences
2022
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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. |
format | Online Article Text |
id | pubmed-9245617 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | National Academy of Sciences |
record_format | MEDLINE/PubMed |
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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