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    Por favor, use este identificador para citar o enlazar este ítem:https://uvadoc.uva.es/handle/10324/74595

    Título
    Urinary Leukotriene E4 and Prostaglandin D2 Metabolites Increase in Adult and Childhood Severe Asthma Characterized by Type 2 Inflammation. A Clinical Observational Study
    Autor
    Kolmert, Johan
    Gómez, Cristina
    Balgoma Hernando, DavidAutoridad UVA Orcid
    Sjödin, Marcus
    Bood, Johan
    Konradsen, Jon R.
    Ericsson, Magnus
    Thörngren, John-Olof
    James, Anna
    Mikus, Maria
    Sousa, Ana R.
    Riley, John H.
    Bates, Stewart
    Bakke, Per S.
    Pandis, Ioannis
    Caruso, Massimo
    Chanez, Pascal
    Fowler, Stephen J.
    Geiser, Thomas
    Howarth, Peter
    Horváth, Ildikó
    Krug, Norbert
    Montuschi, Paolo
    Sanak, Marek
    Behndig, Annelie
    Shaw, Dominick E.
    Knowles, Richard G.
    Holweg, Cécile T. J.
    Wheelock, Åsa M.
    Dahlén, Barbro
    Nordlund, Björn
    Alving, Kjell
    Hedlin, Gunilla
    Chung, Kian Fan
    Adcock, Ian M.
    Sterk, Peter J.
    Djukanovic, Ratko
    Dahlén, Sven-Erik
    Wheelock, Craig E.
    Ahmed, H.
    Auffray, C.
    Bansal, A. T.
    Bel, E. H.
    Bigler, J.
    Billing, B.
    Baribaud, F.
    Bisgaard, H.
    Boedigheimer, M. J.
    Bønnelykke, K.
    Brandsma, J.
    Brinkman, P.
    Bucchioni, E.
    Burg, D.
    Bush, A.
    Chaiboonchoe, A.
    Compton, C. H.
    Corfield, J.
    Cunoosamy, D.
    D’Amico, A.
    De Meulder, B.
    Erpenbeck, V. J.
    Erzen, D.
    Fichtner, K.
    Fitch, N.
    Fleming, L. J.
    Formaggio, E.
    Frey, U.
    Gahlemann, M.
    Goss, V.
    Guo, Y.
    Hashimoto, S.
    Haughney, J.
    Hekking, P. W.
    Higenbottam, T.
    Hohlfeld, J. M.
    Knox, A. J.
    Lazarinis, N.
    Lefaudeux, D.
    Loza, M. J.
    Lutter, R.
    Manta, A.
    Masefield, S.
    Matthews, J. G.
    Mazein, A.
    Meiser, A.
    Middelveld, R. J. M.
    Miralpeix, M.
    Mores, N.
    Murray, C. S.
    Musial, J.
    Myles, D.
    Pahus, L.
    Pavlidis, S.
    Postle, A.
    Powel, P.
    Praticò, G.
    PuigValls, M.
    Rao, N.
    Roberts, A.
    Roberts, G.
    Rowe, A.
    Sandström, T.
    Schofield, J. P. R.
    Seibold, W.
    Selby, A.
    Sigmund, R.
    Singer, F.
    Skipp, P. J.
    Smicker, M.
    Sun, K.
    Thornton, B.
    Uddin, M.
    van Aalderen, W. M.
    van Geest, M.
    Vestbo, J.
    Vissing, N. H.
    Wagener, A. H.
    Wagers, S. S.
    Weiszhart, Z.
    Wilson, S. J.
    Östling, J.
    Año del Documento
    2021
    Editorial
    American Thoracic Society
    Descripción
    Producción Científica
    Documento Fuente
    Am J Respir Crit Care Med. 2021 Jan 1;203(1):37-53
    Resumen
    Rationale: New approaches are needed to guide personalized treatment of asthma.Objectives: To test if urinary eicosanoid metabolites can direct asthma phenotyping.Methods: 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.Measurement and Main Results: Metabolite concentrations in healthy control participants were unrelated to age, body mass index, and sex, except for the PGE2 pathway. Eicosanoid concentrations were generally greater in participants with MMA relative to healthy control participants, with further elevations in participants with SA. However, PGE2 metabolite concentrations were either the same or lower in male nonsmokers with asthma than in healthy control participants. Metabolite concentrations were unchanged in those with asthma who adhered to oral corticosteroid treatment as documented by urinary prednisolone detection, whereas those with SA treated with omalizumab had lower concentrations of LTE4 and the PGD2 metabolite 2,3-dinor-11β-PGF2α. High concentrations of LTE4 and PGD2 metabolites were associated with lower lung function and increased amounts of exhaled nitric oxide and eosinophil markers in blood, sputum, and urine in U-BIOPRED participants and in adolescents with asthma. These type 2 (T2) asthma associations were reproduced in the follow-up visit of the U-BIOPRED study and were found to be as sensitive to detect T2 inflammation as the established biomarkers.Conclusions: Monitoring of urinary eicosanoids can identify T2 asthma and introduces a new noninvasive approach for molecular phenotyping of adult and adolescent asthma.Clinical trial registered with www.clinicaltrials.gov (NCT01976767).
    ISSN
    1073-449X
    Revisión por pares
    SI
    DOI
    10.1164/RCCM.201909-1869OC
    Patrocinador
    Identification of the Molecular Mechanisms of non-response to Treatments, Relapses and Remission in Autoimmune, Inflammatory, and Allergic Conditions Funder: European Commission (EC) Grant agreement ID: 831434-Rcn: 224791-Project acronym: 3TR-DOI: 10.3030/831434
    Version del Editor
    https://www.atsjournals.org/doi/10.1164/rccm.201909-1869OC
    Idioma
    spa
    URI
    https://uvadoc.uva.es/handle/10324/74595
    Tipo de versión
    info:eu-repo/semantics/publishedVersion
    Derechos
    openAccess
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