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Metabolomic Biomarkers in a Model of Asthma Exacerbation: Urine Nuclear Magnetic Resonance
Airway obstruction in patients with asthma is associated with airway dysfunction and inflammation. Objective measurements including sputum analysis can guide therapy, but this is often not possible in typical clinical settings. Metabolomics is the study of molecules generated by metabolic pathways....
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Published in: | American journal of respiratory and critical care medicine 2009-01, Vol.179 (1), p.25-34 |
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creator | Saude, Erik J Obiefuna, Idongesit P Somorjai, Ray L Ajamian, Farnam Skappak, Christopher Ahmad, Taisir Dolenko, Brion K Sykes, Brian D Moqbel, Redwan Adamko, Darryl J |
description | Airway obstruction in patients with asthma is associated with airway dysfunction and inflammation. Objective measurements including sputum analysis can guide therapy, but this is often not possible in typical clinical settings. Metabolomics is the study of molecules generated by metabolic pathways. We hypothesize that airway dysfunction and inflammation in an animal model of asthma would produce unique patterns of urine metabolites measured by multivariate statistical analysis of high-resolution proton nuclear magnetic resonance ((1)H NMR) spectroscopy data.
To develop a noninvasive means of monitoring asthma status by metabolomics and urine sampling.
Five groups of guinea pigs were studied: control, control treated with dexamethasone, sensitized (ovalbumin, administered intraperitoneally), sensitized and challenged (ovalbumin, administered intraperitoneally, plus ovalbumin aerosol), and sensitized-challenged with dexamethasone. Airway hyperreactivity (AHR) to histamine (administered intravenously) and inflammation were measured. Multivariate statistical analysis of NMR spectra based on a library of known urine metabolites was performed by partial least-squares discriminant analysis. In addition, the raw NMR spectra exported as xy-trace data underwent linear discriminant analysis.
Challenged guinea pigs developed AHR and increased inflammation compared with sensitized or control animals. Dexamethasone significantly improved AHR. Using concentration differences in metabolites, partial least-squares discriminant analysis could discriminate challenged animals with 90% accuracy. Using only three or four regions of the NMR spectra, linear discriminant analysis-based classification demonstrated 80-90% separation of the animal groups.
Urine metabolites correlate with airway dysfunction in an asthma model. Urine NMR analysis is a promising, noninvasive technique for monitoring asthma in humans. |
doi_str_mv | 10.1164/rccm.200711-1716OC |
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To develop a noninvasive means of monitoring asthma status by metabolomics and urine sampling.
Five groups of guinea pigs were studied: control, control treated with dexamethasone, sensitized (ovalbumin, administered intraperitoneally), sensitized and challenged (ovalbumin, administered intraperitoneally, plus ovalbumin aerosol), and sensitized-challenged with dexamethasone. Airway hyperreactivity (AHR) to histamine (administered intravenously) and inflammation were measured. Multivariate statistical analysis of NMR spectra based on a library of known urine metabolites was performed by partial least-squares discriminant analysis. In addition, the raw NMR spectra exported as xy-trace data underwent linear discriminant analysis.
Challenged guinea pigs developed AHR and increased inflammation compared with sensitized or control animals. Dexamethasone significantly improved AHR. Using concentration differences in metabolites, partial least-squares discriminant analysis could discriminate challenged animals with 90% accuracy. Using only three or four regions of the NMR spectra, linear discriminant analysis-based classification demonstrated 80-90% separation of the animal groups.
Urine metabolites correlate with airway dysfunction in an asthma model. Urine NMR analysis is a promising, noninvasive technique for monitoring asthma in humans.</description><identifier>ISSN: 1073-449X</identifier><identifier>EISSN: 1535-4970</identifier><identifier>DOI: 10.1164/rccm.200711-1716OC</identifier><identifier>PMID: 18931331</identifier><language>eng</language><publisher>New York, NY: Am Thoracic Soc</publisher><subject>Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy ; Animals ; Asthma - physiopathology ; Asthma - urine ; Biological and medical sciences ; Biomarkers ; Biomarkers - urine ; Chronic obstructive pulmonary disease, asthma ; Discriminant Analysis ; Female ; Guinea Pigs ; Intensive care medicine ; Least-Squares Analysis ; Magnetic Resonance Spectroscopy ; Medical sciences ; Metabolites ; Metabolomics ; Models, Animal ; NMR ; Nuclear magnetic resonance ; Pneumology ; Spectrum analysis</subject><ispartof>American journal of respiratory and critical care medicine, 2009-01, Vol.179 (1), p.25-34</ispartof><rights>2009 INIST-CNRS</rights><rights>Copyright American Thoracic Society Jan 1, 2009</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c391t-2992fdb0ffb5d0e8bfb1d507da979d36091e11207b83757fd6c28996fca702cb3</citedby><cites>FETCH-LOGICAL-c391t-2992fdb0ffb5d0e8bfb1d507da979d36091e11207b83757fd6c28996fca702cb3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,4024,27923,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=21005756$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/18931331$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Saude, Erik J</creatorcontrib><creatorcontrib>Obiefuna, Idongesit P</creatorcontrib><creatorcontrib>Somorjai, Ray L</creatorcontrib><creatorcontrib>Ajamian, Farnam</creatorcontrib><creatorcontrib>Skappak, Christopher</creatorcontrib><creatorcontrib>Ahmad, Taisir</creatorcontrib><creatorcontrib>Dolenko, Brion K</creatorcontrib><creatorcontrib>Sykes, Brian D</creatorcontrib><creatorcontrib>Moqbel, Redwan</creatorcontrib><creatorcontrib>Adamko, Darryl J</creatorcontrib><title>Metabolomic Biomarkers in a Model of Asthma Exacerbation: Urine Nuclear Magnetic Resonance</title><title>American journal of respiratory and critical care medicine</title><addtitle>Am J Respir Crit Care Med</addtitle><description>Airway obstruction in patients with asthma is associated with airway dysfunction and inflammation. Objective measurements including sputum analysis can guide therapy, but this is often not possible in typical clinical settings. Metabolomics is the study of molecules generated by metabolic pathways. We hypothesize that airway dysfunction and inflammation in an animal model of asthma would produce unique patterns of urine metabolites measured by multivariate statistical analysis of high-resolution proton nuclear magnetic resonance ((1)H NMR) spectroscopy data.
To develop a noninvasive means of monitoring asthma status by metabolomics and urine sampling.
Five groups of guinea pigs were studied: control, control treated with dexamethasone, sensitized (ovalbumin, administered intraperitoneally), sensitized and challenged (ovalbumin, administered intraperitoneally, plus ovalbumin aerosol), and sensitized-challenged with dexamethasone. Airway hyperreactivity (AHR) to histamine (administered intravenously) and inflammation were measured. Multivariate statistical analysis of NMR spectra based on a library of known urine metabolites was performed by partial least-squares discriminant analysis. In addition, the raw NMR spectra exported as xy-trace data underwent linear discriminant analysis.
Challenged guinea pigs developed AHR and increased inflammation compared with sensitized or control animals. Dexamethasone significantly improved AHR. Using concentration differences in metabolites, partial least-squares discriminant analysis could discriminate challenged animals with 90% accuracy. Using only three or four regions of the NMR spectra, linear discriminant analysis-based classification demonstrated 80-90% separation of the animal groups.
Urine metabolites correlate with airway dysfunction in an asthma model. Urine NMR analysis is a promising, noninvasive technique for monitoring asthma in humans.</description><subject>Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy</subject><subject>Animals</subject><subject>Asthma - physiopathology</subject><subject>Asthma - urine</subject><subject>Biological and medical sciences</subject><subject>Biomarkers</subject><subject>Biomarkers - urine</subject><subject>Chronic obstructive pulmonary disease, asthma</subject><subject>Discriminant Analysis</subject><subject>Female</subject><subject>Guinea Pigs</subject><subject>Intensive care medicine</subject><subject>Least-Squares Analysis</subject><subject>Magnetic Resonance Spectroscopy</subject><subject>Medical sciences</subject><subject>Metabolites</subject><subject>Metabolomics</subject><subject>Models, Animal</subject><subject>NMR</subject><subject>Nuclear magnetic resonance</subject><subject>Pneumology</subject><subject>Spectrum analysis</subject><issn>1073-449X</issn><issn>1535-4970</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2009</creationdate><recordtype>article</recordtype><recordid>eNpdkE1rFTEUQIMotlb_gAsJguJmam4ymUzc1Uf9gD4LYkHchCST9OWZmdRkBvXfm8c8FFzlLs49NxyEngI5B-ja19na8ZwSIgAaENBdb-6hU-CMN60U5H6diWBN28qvJ-hRKXtCgPZAHqIT6CUDxuAUfdu6WZsU0xgsfhvSqPN3lwsOE9Z4mwYXcfL4osy7UePLX9q6bPQc0vQG3-QwOfxpsdHpjLf6dnJzlXx2JU16su4xeuB1LO7J8T1DN-8uv2w-NFfX7z9uLq4ayyTMDZWS-sEQ7w0fiOuNNzBwIgYthRxYRyQ4AEqE6Zngwg-dpb2UnbdaEGoNO0MvV-9dTj8WV2Y1hmJdjHpyaSmq60QrOGUVfP4fuE9LnurfFFQh6aHnFaIrZHMqJTuv7nKoVX4rIOqQXR2yqzW7WrPXpWdH82JGN_xbOXauwIsjoIvV0ecaKJS_HAVCuOBd5V6t3C7c7n6G7FQZdYxVC0rvD5dBSAWKcvYH5H-ZDg</recordid><startdate>20090101</startdate><enddate>20090101</enddate><creator>Saude, Erik J</creator><creator>Obiefuna, Idongesit P</creator><creator>Somorjai, Ray L</creator><creator>Ajamian, Farnam</creator><creator>Skappak, Christopher</creator><creator>Ahmad, Taisir</creator><creator>Dolenko, Brion K</creator><creator>Sykes, Brian D</creator><creator>Moqbel, Redwan</creator><creator>Adamko, Darryl J</creator><general>Am Thoracic Soc</general><general>American Thoracic Society</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7RV</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8C1</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AN0</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>KB0</scope><scope>M0S</scope><scope>M1P</scope><scope>NAPCQ</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope></search><sort><creationdate>20090101</creationdate><title>Metabolomic Biomarkers in a Model of Asthma Exacerbation: Urine Nuclear Magnetic Resonance</title><author>Saude, Erik J ; Obiefuna, Idongesit P ; Somorjai, Ray L ; Ajamian, Farnam ; Skappak, Christopher ; Ahmad, Taisir ; Dolenko, Brion K ; Sykes, Brian D ; Moqbel, Redwan ; Adamko, Darryl J</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c391t-2992fdb0ffb5d0e8bfb1d507da979d36091e11207b83757fd6c28996fca702cb3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2009</creationdate><topic>Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy</topic><topic>Animals</topic><topic>Asthma - physiopathology</topic><topic>Asthma - urine</topic><topic>Biological and medical sciences</topic><topic>Biomarkers</topic><topic>Biomarkers - urine</topic><topic>Chronic obstructive pulmonary disease, asthma</topic><topic>Discriminant Analysis</topic><topic>Female</topic><topic>Guinea Pigs</topic><topic>Intensive care medicine</topic><topic>Least-Squares Analysis</topic><topic>Magnetic Resonance Spectroscopy</topic><topic>Medical sciences</topic><topic>Metabolites</topic><topic>Metabolomics</topic><topic>Models, Animal</topic><topic>NMR</topic><topic>Nuclear magnetic resonance</topic><topic>Pneumology</topic><topic>Spectrum analysis</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Saude, Erik J</creatorcontrib><creatorcontrib>Obiefuna, Idongesit P</creatorcontrib><creatorcontrib>Somorjai, Ray L</creatorcontrib><creatorcontrib>Ajamian, Farnam</creatorcontrib><creatorcontrib>Skappak, Christopher</creatorcontrib><creatorcontrib>Ahmad, Taisir</creatorcontrib><creatorcontrib>Dolenko, Brion K</creatorcontrib><creatorcontrib>Sykes, Brian D</creatorcontrib><creatorcontrib>Moqbel, Redwan</creatorcontrib><creatorcontrib>Adamko, Darryl J</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>ProQuest Nursing and Allied Health Journals</collection><collection>ProQuest Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>ProQuest Public Health Database</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central UK/Ireland</collection><collection>British Nursing Database</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Database (Alumni Edition)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>PML(ProQuest Medical Library)</collection><collection>Nursing & Allied Health Premium</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>MEDLINE - Academic</collection><jtitle>American journal of respiratory and critical care medicine</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Saude, Erik J</au><au>Obiefuna, Idongesit P</au><au>Somorjai, Ray L</au><au>Ajamian, Farnam</au><au>Skappak, Christopher</au><au>Ahmad, Taisir</au><au>Dolenko, Brion K</au><au>Sykes, Brian D</au><au>Moqbel, Redwan</au><au>Adamko, Darryl J</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Metabolomic Biomarkers in a Model of Asthma Exacerbation: Urine Nuclear Magnetic Resonance</atitle><jtitle>American journal of respiratory and critical care medicine</jtitle><addtitle>Am J Respir Crit Care Med</addtitle><date>2009-01-01</date><risdate>2009</risdate><volume>179</volume><issue>1</issue><spage>25</spage><epage>34</epage><pages>25-34</pages><issn>1073-449X</issn><eissn>1535-4970</eissn><abstract>Airway obstruction in patients with asthma is associated with airway dysfunction and inflammation. Objective measurements including sputum analysis can guide therapy, but this is often not possible in typical clinical settings. Metabolomics is the study of molecules generated by metabolic pathways. We hypothesize that airway dysfunction and inflammation in an animal model of asthma would produce unique patterns of urine metabolites measured by multivariate statistical analysis of high-resolution proton nuclear magnetic resonance ((1)H NMR) spectroscopy data.
To develop a noninvasive means of monitoring asthma status by metabolomics and urine sampling.
Five groups of guinea pigs were studied: control, control treated with dexamethasone, sensitized (ovalbumin, administered intraperitoneally), sensitized and challenged (ovalbumin, administered intraperitoneally, plus ovalbumin aerosol), and sensitized-challenged with dexamethasone. Airway hyperreactivity (AHR) to histamine (administered intravenously) and inflammation were measured. Multivariate statistical analysis of NMR spectra based on a library of known urine metabolites was performed by partial least-squares discriminant analysis. In addition, the raw NMR spectra exported as xy-trace data underwent linear discriminant analysis.
Challenged guinea pigs developed AHR and increased inflammation compared with sensitized or control animals. Dexamethasone significantly improved AHR. Using concentration differences in metabolites, partial least-squares discriminant analysis could discriminate challenged animals with 90% accuracy. Using only three or four regions of the NMR spectra, linear discriminant analysis-based classification demonstrated 80-90% separation of the animal groups.
Urine metabolites correlate with airway dysfunction in an asthma model. Urine NMR analysis is a promising, noninvasive technique for monitoring asthma in humans.</abstract><cop>New York, NY</cop><pub>Am Thoracic Soc</pub><pmid>18931331</pmid><doi>10.1164/rccm.200711-1716OC</doi><tpages>10</tpages></addata></record> |
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subjects | Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy Animals Asthma - physiopathology Asthma - urine Biological and medical sciences Biomarkers Biomarkers - urine Chronic obstructive pulmonary disease, asthma Discriminant Analysis Female Guinea Pigs Intensive care medicine Least-Squares Analysis Magnetic Resonance Spectroscopy Medical sciences Metabolites Metabolomics Models, Animal NMR Nuclear magnetic resonance Pneumology Spectrum analysis |
title | Metabolomic Biomarkers in a Model of Asthma Exacerbation: Urine Nuclear Magnetic Resonance |
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