Please use this identifier to cite or link to this item: http://hdl.handle.net/2445/177028
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dc.contributor.authorEgli, Adrian-
dc.contributor.authorMandal, Jyotshna-
dc.contributor.authorSchumann, Desiree M.-
dc.contributor.authorRoth, Michael-
dc.contributor.authorThomas, Brad-
dc.contributor.authorTyrrell, D. Lorne-
dc.contributor.authorBlasi, Francesco-
dc.contributor.authorKostikas, Kostantinos-
dc.contributor.authorBoersma, Wim-
dc.contributor.authorMilenkovic, Branislava-
dc.contributor.authorLacoma, Alicia-
dc.contributor.authorRentsch, Katharina-
dc.contributor.authorRohde, Gernot G. U.-
dc.contributor.authorLouis, Renaud-
dc.contributor.authorAerts, Joachim G.-
dc.contributor.authorWelte, Tobias-
dc.contributor.authorTorres Martí, Antoni-
dc.contributor.authorTamm, Michael-
dc.contributor.authorStolz, Daiana-
dc.date.accessioned2021-05-05T15:39:42Z-
dc.date.available2021-05-05T15:39:42Z-
dc.date.issued2018-03-21-
dc.identifier.issn1471-2466-
dc.identifier.urihttp://hdl.handle.net/2445/177028-
dc.description.abstractBackground: Interferon lambdas (IFNLs) have important anti-viral/bacterial and immunomodulatory functions in the respiratory tract. How do IFNLs impact COPD and its exacerbations? Methods: Five hundred twenty eight patients were recruited in a prospective observational multicentre cohort (PROMISE) study. The genetic polymorphisms (rs8099917 and rs12979860) within the IFNL3/4 gene region and circulating levels of IFNL3 in COPD patients were determined and associated with disease activity and outcome during a median follow-up of 24 months. Results: The GG genotype significantly influenced severe exacerbation rate (42 vs. 23%; p = 0.032) and time to severe exacerbation (HR = 2.260; p = 0.012). Compared to the TT or TG genotypes, the GG genotype was associated with severe dyspnoea (modified medical research council score ≥ median 3; 22 vs 42%, p = 0.030). The CC genotype of the rs12979860 SNP was associated with a poorer prognosis (body mass index, airflow obstruction, dyspnea and exercise capacity index ≥ median 4; 46 vs. 36% TC vs. 20.5% TT; p = 0.031). Patients with stable COPD and at exacerbation had significantly lower circulating IFNL3 compared to healthy controls (p < 0.001 and p < 0.001, respectively). Circulating IFNL3 correlated to post-bronchodilator FEV1%predicted and the tissue maturation biomarker Pro-collagen 3. Conclusion: IFNL3/4 polymorphisms and circulating IFNL3 may be associated with disease activity and outcomes in COPD. Trial registration: Clinical Trial registration http://www.isrctn.com/ identifier ISRCTN99586989 on 16 April 2008.-
dc.format.extent9 p.-
dc.format.mimetypeapplication/pdf-
dc.language.isoeng-
dc.publisherBioMed Central-
dc.relation.isformatofReproducció del document publicat a: https://doi.org/10.1186/s12890-018-0616-6-
dc.relation.ispartofBMC Pulmonary Medicine, 2018, vol. 18, num. 1, p. 51-
dc.relation.urihttps://doi.org/10.1186/s12890-018-0616-6-
dc.rightscc-by (c) Egli, Adrian et al., 2018-
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/es-
dc.sourceArticles publicats en revistes (Medicina)-
dc.subject.classificationMortalitat-
dc.subject.classificationMarcadors bioquímics-
dc.subject.classificationPolimorfisme genètic-
dc.subject.otherMortality-
dc.subject.otherBiochemical markers-
dc.subject.otherGenetic polymorphisms-
dc.titleIFN Lambda 3/4 locus polymorphisms and IFN Lambda 3 circulating levels are associated with COPD severity and outcomes-
dc.typeinfo:eu-repo/semantics/article-
dc.typeinfo:eu-repo/semantics/publishedVersion-
dc.identifier.idgrec697314-
dc.date.updated2021-05-05T15:39:42Z-
dc.rights.accessRightsinfo:eu-repo/semantics/openAccess-
Appears in Collections:Articles publicats en revistes (Medicina)

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