<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Kolmert J</submitter><funding>Medical Research Council</funding><funding>National Institute for Health Research (NIHR)</funding><pagination>37-53</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC7781128</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>203(1)</volume><pubmed_abstract>&lt;b>Rationale:&lt;/b> New approaches are needed to guide personalized treatment of asthma.&lt;b>Objectives:&lt;/b> To test if urinary eicosanoid metabolites can direct asthma phenotyping.&lt;b>Methods:&lt;/b> Urinary metabolites of prostaglandins (PGs), cysteinyl leukotrienes (CysLTs), and isoprostanes were quantified in the U-BIOPRED (Unbiased Biomarkers for the Prediction of Respiratory Diseases Outcomes) study including 86 adults with mild-to-moderate asthma (MMA), 411 with severe asthma (SA), and 100 healthy control participants. Validation was performed internally in 302 participants with SA followed up after 12-18 months and externally in 95 adolescents with asthma.&lt;b>Measurement and Main Results:&lt;/b> Metabolite concentrations in healthy control participants were unrelated to age, body mass index, a</pubmed_abstract><journal>American journal of respiratory and critical care medicine</journal><pubmed_title>Urinary Leukotriene E&amp;lt;sub&amp;gt;4&amp;lt;/sub&amp;gt; and Prostaglandin D&amp;lt;sub&amp;gt;2&amp;lt;/sub&amp;gt; Metabolites Increase in Adult and Childhood Severe Asthma Characterized by Type 2 Inflammation. A Clinical Observational Study.</pubmed_title><pmcid>PMC7781128</pmcid><funding_grant_id>NIHR200199</funding_grant_id><funding_grant_id>MR/N005953/1</funding_grant_id><pubmed_authors>Hedlin G</pubmed_authors><pubmed_authors>D'Amico A</pubmed_authors><pubmed_authors>Boedigheimer MJ</pubmed_authors><pubmed_authors>Guo Y</pubmed_authors><pubmed_authors>James A</pubmed_authors><pubmed_authors>Gomez C</pubmed_authors><pubmed_authors>Cunoosamy D</pubmed_authors><pubmed_authors>Pratico G</pubmed_authors><pubmed_authors>Rowe A</pubmed_authors><pubmed_authors>Skipp PJ</pubmed_authors><pubmed_authors>Caruso M</pubmed_authors><pubmed_authors>Ahmed H</pubmed_authors><pubmed_authors>Pavlidis S</pubmed_authors><pubmed_authors>Postle A</pubmed_authors><pubmed_authors>Bonnelykke K</pubmed_authors><pubmed_authors>Adcock IM</pubmed_authors><pubmed_authors>Brinkman P</pubmed_authors><pubmed_authors>Erzen D</pubmed_authors><pubmed_authors>Pahus L</pubmed_authors><pubmed_authors>Chanez 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A Clinical Observational Study.</name><description>&lt;b>Rationale:&lt;/b> New approaches are needed to guide personalized treatment of asthma.&lt;b>Objectives:&lt;/b> To test if urinary eicosanoid metabolites can direct asthma phenotyping.&lt;b>Methods:&lt;/b> Urinary metabolites of prostaglandins (PGs), cysteinyl leukotrienes (CysLTs), and isoprostanes were quantified in the U-BIOPRED (Unbiased Biomarkers for the Prediction of Respiratory Diseases Outcomes) study including 86 adults with mild-to-moderate asthma (MMA), 411 with severe asthma (SA), and 100 healthy control participants. Validation was performed internally in 302 participants with SA followed up after 12-18 months and externally in 95 adolescents with asthma.&lt;b>Measurement and Main Results:&lt;/b> Metabolite concentrations in healthy control participants were unrelated to age, body mass index, a</description><dates><release>2021-01-01T00:00:00Z</release><publication>2021 Jan</publication><modification>2026-06-02T16:19:45.32Z</modification><creation>2022-02-09T17:36:40.447Z</creation></dates><accession>S-EPMC7781128</accession><cross_references><pubmed>32667261</pubmed><doi>10.1164/rccm.201909-1869OC</doi></cross_references></HashMap>