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Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations
The study of metabolomics and disease has enabled the discovery of new risk factors, diagnostic markers, and drug targets. For neurological and psychiatric phenotypes, the cerebrospinal fluid (CSF) is of particular importance. However, the CSF metabolome is difficult to study on a large scale due to...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7803963/ https://www.ncbi.nlm.nih.gov/pubmed/33437055 http://dx.doi.org/10.1038/s42003-020-01583-z |
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author | Panyard, Daniel J. Kim, Kyeong Mo Darst, Burcu F. Deming, Yuetiva K. Zhong, Xiaoyuan Wu, Yuchang Kang, Hyunseung Carlsson, Cynthia M. Johnson, Sterling C. Asthana, Sanjay Engelman, Corinne D. Lu, Qiongshi |
author_facet | Panyard, Daniel J. Kim, Kyeong Mo Darst, Burcu F. Deming, Yuetiva K. Zhong, Xiaoyuan Wu, Yuchang Kang, Hyunseung Carlsson, Cynthia M. Johnson, Sterling C. Asthana, Sanjay Engelman, Corinne D. Lu, Qiongshi |
author_sort | Panyard, Daniel J. |
collection | PubMed |
description | The study of metabolomics and disease has enabled the discovery of new risk factors, diagnostic markers, and drug targets. For neurological and psychiatric phenotypes, the cerebrospinal fluid (CSF) is of particular importance. However, the CSF metabolome is difficult to study on a large scale due to the relative complexity of the procedure needed to collect the fluid. Here, we present a metabolome-wide association study (MWAS), which uses genetic and metabolomic data to impute metabolites into large samples with genome-wide association summary statistics. We conduct a metabolome-wide, genome-wide association analysis with 338 CSF metabolites, identifying 16 genotype-metabolite associations (metabolite quantitative trait loci, or mQTLs). We then build prediction models for all available CSF metabolites and test for associations with 27 neurological and psychiatric phenotypes, identifying 19 significant CSF metabolite-phenotype associations. Our results demonstrate the feasibility of MWAS to study omic data in scarce sample types. |
format | Online Article Text |
id | pubmed-7803963 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-78039632021-01-21 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations Panyard, Daniel J. Kim, Kyeong Mo Darst, Burcu F. Deming, Yuetiva K. Zhong, Xiaoyuan Wu, Yuchang Kang, Hyunseung Carlsson, Cynthia M. Johnson, Sterling C. Asthana, Sanjay Engelman, Corinne D. Lu, Qiongshi Commun Biol Article The study of metabolomics and disease has enabled the discovery of new risk factors, diagnostic markers, and drug targets. For neurological and psychiatric phenotypes, the cerebrospinal fluid (CSF) is of particular importance. However, the CSF metabolome is difficult to study on a large scale due to the relative complexity of the procedure needed to collect the fluid. Here, we present a metabolome-wide association study (MWAS), which uses genetic and metabolomic data to impute metabolites into large samples with genome-wide association summary statistics. We conduct a metabolome-wide, genome-wide association analysis with 338 CSF metabolites, identifying 16 genotype-metabolite associations (metabolite quantitative trait loci, or mQTLs). We then build prediction models for all available CSF metabolites and test for associations with 27 neurological and psychiatric phenotypes, identifying 19 significant CSF metabolite-phenotype associations. Our results demonstrate the feasibility of MWAS to study omic data in scarce sample types. Nature Publishing Group UK 2021-01-12 /pmc/articles/PMC7803963/ /pubmed/33437055 http://dx.doi.org/10.1038/s42003-020-01583-z Text en © The Author(s) 2021 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 Panyard, Daniel J. Kim, Kyeong Mo Darst, Burcu F. Deming, Yuetiva K. Zhong, Xiaoyuan Wu, Yuchang Kang, Hyunseung Carlsson, Cynthia M. Johnson, Sterling C. Asthana, Sanjay Engelman, Corinne D. Lu, Qiongshi Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations |
title | Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations |
title_full | Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations |
title_fullStr | Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations |
title_full_unstemmed | Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations |
title_short | Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations |
title_sort | cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7803963/ https://www.ncbi.nlm.nih.gov/pubmed/33437055 http://dx.doi.org/10.1038/s42003-020-01583-z |
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