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The metabolomics of asthma control: a promising link between genetics and disease

Short-acting β agonists (e.g., albuterol) are the most commonly used medications for asthma, a disease that affects over 300 million people in the world. Metabolomic profiling of asthmatics taking β agonists presents a new and promising resource for identifying the molecular determinants of asthma c...

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Autores principales: McGeachie, Michael J, Dahlin, Amber, Qiu, Weiliang, Croteau-Chonka, Damien C, Savage, Jessica, Wu, Ann Chen, Wan, Emily S, Sordillo, Joanne E, Al-Garawi, Amal, Martinez, Fernando D, Strunk, Robert C, Lemanske, Robert F, Liu, Andrew H, Raby, Benjamin A, Weiss, Scott, Clish, Clary B, Lasky-Su, Jessica A
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons, Ltd 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4578522/
https://www.ncbi.nlm.nih.gov/pubmed/26421150
http://dx.doi.org/10.1002/iid3.61
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author McGeachie, Michael J
Dahlin, Amber
Qiu, Weiliang
Croteau-Chonka, Damien C
Savage, Jessica
Wu, Ann Chen
Wan, Emily S
Sordillo, Joanne E
Al-Garawi, Amal
Martinez, Fernando D
Strunk, Robert C
Lemanske, Robert F
Liu, Andrew H
Raby, Benjamin A
Weiss, Scott
Clish, Clary B
Lasky-Su, Jessica A
author_facet McGeachie, Michael J
Dahlin, Amber
Qiu, Weiliang
Croteau-Chonka, Damien C
Savage, Jessica
Wu, Ann Chen
Wan, Emily S
Sordillo, Joanne E
Al-Garawi, Amal
Martinez, Fernando D
Strunk, Robert C
Lemanske, Robert F
Liu, Andrew H
Raby, Benjamin A
Weiss, Scott
Clish, Clary B
Lasky-Su, Jessica A
author_sort McGeachie, Michael J
collection PubMed
description Short-acting β agonists (e.g., albuterol) are the most commonly used medications for asthma, a disease that affects over 300 million people in the world. Metabolomic profiling of asthmatics taking β agonists presents a new and promising resource for identifying the molecular determinants of asthma control. The objective is to identify novel genetic and biochemical predictors of asthma control using an integrative “omics” approach. We generated lipidomic data by liquid chromatography tandem mass spectrometry (LC-MS), ­ using plasma samples from 20 individuals with asthma. The outcome of interest was a binary indicator of asthma control defined by the use of albuterol inhalers in the preceding week. We integrated metabolomic data with genome-wide genotype, gene expression, and methylation data of this cohort to identify genomic and molecular indicators of asthma control. A Conditional Gaussian Bayesian Network (CGBN) was generated using the strongest predictors from each of these analyses. Integrative and metabolic pathway over-representation analyses (ORA) identified enrichment of known biological pathways within the strongest molecular determinants. Of the 64 metabolites measured, 32 had known identities. The CGBN model based on four SNPs (rs9522789, rs7147228, rs2701423, rs759582) and two metabolites—monoHETE_0863 and sphingosine-1-phosphate (S1P) could predict asthma control with an AUC of 95%. Integrative ORA identified 17 significantly enriched pathways related to cellular immune response, interferon signaling, and cytokine-related signaling, for which arachidonic acid, PGE2 and S1P, in addition to six genes (CHN1, PRKCE, GNA12, OASL, OAS1, and IFIT3) appeared to drive the pathway results. Of these predictors, S1P, GNA12, and PRKCE were enriched in the results from integrative and metabolic ORAs. Through an integrative analysis of metabolomic, genomic, and methylation data from a small cohort of asthmatics, we implicate altered metabolic pathways, related to sphingolipid metabolism, in asthma control. These results provide insight into the pathophysiology of asthma control.
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spelling pubmed-45785222015-09-29 The metabolomics of asthma control: a promising link between genetics and disease McGeachie, Michael J Dahlin, Amber Qiu, Weiliang Croteau-Chonka, Damien C Savage, Jessica Wu, Ann Chen Wan, Emily S Sordillo, Joanne E Al-Garawi, Amal Martinez, Fernando D Strunk, Robert C Lemanske, Robert F Liu, Andrew H Raby, Benjamin A Weiss, Scott Clish, Clary B Lasky-Su, Jessica A Immun Inflamm Dis Original Research Short-acting β agonists (e.g., albuterol) are the most commonly used medications for asthma, a disease that affects over 300 million people in the world. Metabolomic profiling of asthmatics taking β agonists presents a new and promising resource for identifying the molecular determinants of asthma control. The objective is to identify novel genetic and biochemical predictors of asthma control using an integrative “omics” approach. We generated lipidomic data by liquid chromatography tandem mass spectrometry (LC-MS), ­ using plasma samples from 20 individuals with asthma. The outcome of interest was a binary indicator of asthma control defined by the use of albuterol inhalers in the preceding week. We integrated metabolomic data with genome-wide genotype, gene expression, and methylation data of this cohort to identify genomic and molecular indicators of asthma control. A Conditional Gaussian Bayesian Network (CGBN) was generated using the strongest predictors from each of these analyses. Integrative and metabolic pathway over-representation analyses (ORA) identified enrichment of known biological pathways within the strongest molecular determinants. Of the 64 metabolites measured, 32 had known identities. The CGBN model based on four SNPs (rs9522789, rs7147228, rs2701423, rs759582) and two metabolites—monoHETE_0863 and sphingosine-1-phosphate (S1P) could predict asthma control with an AUC of 95%. Integrative ORA identified 17 significantly enriched pathways related to cellular immune response, interferon signaling, and cytokine-related signaling, for which arachidonic acid, PGE2 and S1P, in addition to six genes (CHN1, PRKCE, GNA12, OASL, OAS1, and IFIT3) appeared to drive the pathway results. Of these predictors, S1P, GNA12, and PRKCE were enriched in the results from integrative and metabolic ORAs. Through an integrative analysis of metabolomic, genomic, and methylation data from a small cohort of asthmatics, we implicate altered metabolic pathways, related to sphingolipid metabolism, in asthma control. These results provide insight into the pathophysiology of asthma control. John Wiley & Sons, Ltd 2015-09 2015-05-07 /pmc/articles/PMC4578522/ /pubmed/26421150 http://dx.doi.org/10.1002/iid3.61 Text en © 2015 The Authors. Immunity, Inflammation and Disease Published by John Wiley & Sons Ltd. http://creativecommons.org/licenses/by/4.0/ This is an open access article under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Research
McGeachie, Michael J
Dahlin, Amber
Qiu, Weiliang
Croteau-Chonka, Damien C
Savage, Jessica
Wu, Ann Chen
Wan, Emily S
Sordillo, Joanne E
Al-Garawi, Amal
Martinez, Fernando D
Strunk, Robert C
Lemanske, Robert F
Liu, Andrew H
Raby, Benjamin A
Weiss, Scott
Clish, Clary B
Lasky-Su, Jessica A
The metabolomics of asthma control: a promising link between genetics and disease
title The metabolomics of asthma control: a promising link between genetics and disease
title_full The metabolomics of asthma control: a promising link between genetics and disease
title_fullStr The metabolomics of asthma control: a promising link between genetics and disease
title_full_unstemmed The metabolomics of asthma control: a promising link between genetics and disease
title_short The metabolomics of asthma control: a promising link between genetics and disease
title_sort metabolomics of asthma control: a promising link between genetics and disease
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4578522/
https://www.ncbi.nlm.nih.gov/pubmed/26421150
http://dx.doi.org/10.1002/iid3.61
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