Identification and prospective validation of clinically relevant chronic obstructive pulmonary disease (COPD) subtypes

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.date.updated2013-09-27T10:02:31Z
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.identifier.idgrec609851
dc.identifier.issn0040-6376
dc.identifier.pmid21177668
dc.identifier.urihttps://hdl.handle.net/2445/46391
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.rights.accessRightsinfo:eu-repo/semantics/openAccess
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

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