Please use this identifier to cite or link to this item: http://hdl.handle.net/2445/46391
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dc.contributor.authorGarcía Aymerich, Judith-
dc.contributor.authorGomez, Federico P.-
dc.contributor.authorBenet Mora, Marta-
dc.contributor.authorFarrero, Eva-
dc.contributor.authorBasagaña, Xavier-
dc.contributor.authorGayete, Àngel-
dc.contributor.authorPare i Bardera, J. Carles-
dc.contributor.authorFreixa, Xavier-
dc.contributor.authorFerrer, Jaume-
dc.contributor.authorFerrer Monreal, Antonio-
dc.contributor.authorRoca Elias, Josep-
dc.contributor.authorGaldiz, Juan B.-
dc.contributor.authorSauleda, Jaume-
dc.contributor.authorMonsó, Eduard-
dc.contributor.authorGea Guiral, Joaquim-
dc.contributor.authorBarberà i Mir, Joan Albert-
dc.contributor.authorAgustí García-Navarro, Àlvar-
dc.contributor.authorAntó i Boqué, Josep Maria-
dc.date.accessioned2013-09-27T10:02:31Z-
dc.date.available2013-09-27T10:02:31Z-
dc.date.issued2010-12-21-
dc.identifier.issn0040-6376-
dc.identifier.urihttp://hdl.handle.net/2445/46391-
dc.description.abstractBackground Chronic obstructive pulmonary disease (COPD) is increasingly considered a heterogeneous condition. It was hypothesised that COPD, as currently defined, includes different clinically relevant subtypes. Methods To identify and validate COPD subtypes, 342 subjects hospitalised for the first time because of a COPD exacerbation were recruited. Three months after discharge, when clinically stable, symptoms and quality of life, lung function, exercise capacity, nutritional status, biomarkers of systemic and bronchial inflammation, sputum microbiology, CT of the thorax and echocardiography were assessed. COPD groups were identified by partitioning cluster analysis and validated prospectively against cause-specific hospitalisations and all-cause mortality during a 4 year follow-up. Results Three COPD groups were identified: group 1 (n ¼ 126, 67 years) was characterised by severe airflow limitation (postbronchodilator forced expiratory volume in 1 s (FEV 1 ) 38% predicted) and worse performance in most of the respiratory domains of the disease; group 2 (n ¼ 125, 69 years) showed milder airflow limitation (FEV 1 63% predicted); and group 3 (n ¼ 91, 67 years) combined a similarly milder airflow limitation (FEV 1 58% predicted) with a high proportion of obesity, cardiovascular disorders, iabetes and systemic inflammation. During follow-up, group 1 had more frequent hospitalisations due to COPD (HR 3.28, p < 0.001) and higher all-cause mortality (HR 2.36, p ¼ 0.018) than the other two groups, whereas group 3 had more admissions due to cardiovascular disease (HR 2.87, p ¼ 0.014). Conclusions In patients with COPD recruited at their first hospitalisation, three different COPD subtypes were identified and prospectively validated:"severe respiratory COPD","moderate respiratory COPD", and"systemic COPD'-
dc.format.extent9 p.-
dc.format.mimetypeapplication/pdf-
dc.language.isoeng-
dc.publisherBMJ Publishing Group-
dc.relation.isformatofReproducció del document publicat a: http://dx.doi.org/10.1136/thx.2010.154484-
dc.relation.ispartofThorax, 2010, vol. 66, p. 430-437-
dc.relation.urihttp://dx.doi.org/10.1136/thx.2010.154484-
dc.rights(c) BMJ Publishing Group, 2010-
dc.sourceArticles publicats en revistes (Medicina)-
dc.subject.classificationMalalties de l'aparell respiratori-
dc.subject.classificationMalalties pulmonars obstructives cròniques-
dc.subject.classificationAssaigs clínics-
dc.subject.otherRespiratory organs diseases-
dc.subject.otherChronic obstructive pulmonary diseases-
dc.subject.otherClinical trials-
dc.titleIdentification and prospective validation of clinically relevant chronic obstructive pulmonary disease (COPD) subtypes-
dc.typeinfo:eu-repo/semantics/article-
dc.typeinfo:eu-repo/semantics/publishedVersion-
dc.identifier.idgrec609851-
dc.date.updated2013-09-27T10:02:31Z-
dc.rights.accessRightsinfo:eu-repo/semantics/openAccess-
dc.identifier.pmid21177668-
Appears in Collections:Articles publicats en revistes (Medicina)

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