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

Open access
Garcia-Aymerich, J., Gomez, F. P., Benet, M., Farrero, E., Basagana, X., Gayete, A., Pare, C., Freixa, X., Ferrer, J., Ferrer, A., Roca, J., Galdiz, J. B., Sauleda, J., Monso, E., Gea, J., Barbera, J. A., Agusti, A., Anto, J. M., on behalf of the PAC-COPD Study Group·2011·Thorax

Abstract

BACKGROUND: 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=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=125, 69 years) showed milder airflow limitation (FEV(1) 63% predicted); and group 3 (n=91, 67 years) combined a similarly milder airflow limitation (FEV(1) 58% predicted) with a high proportion of obesity, cardiovascular disorders, diabetes 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=0.018) than the other two groups, whereas group 3 had more admissions due to cardiovascular disease (HR 2.87, p=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'.

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Metadata

Authors
Garcia-Aymerich, J., Gomez, F. P., Benet, M., Farrero, E., Basagana, X., Gayete, A., Pare, C., Freixa, X., Ferrer, J., Ferrer, A., Roca, J., Galdiz, J. B., Sauleda, J., Monso, E., Gea, J., Barbera, J. A., Agusti, A., Anto, J. M., & on behalf of the PAC-COPD Study Group
Venue
Thorax
Publisher
BMJ
Published
2010-12-21
Volume
66
Issue
5
Pages
430-437
ISSN
0040-6376 (ISSN-L)
OpenAlex
W2109676782
Cited by
319
References
3
FWCI
19.92
Type
journal article
Language
en
Open access
bronze

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CoChat. (2026). Citation check: Identification and prospective validation of clinically relevant chronic obstructive pulmonary disease (COPD) subtypes. https://app.cochat.ai/papers/10.1136/thx.2010.154484
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Garcia-Aymerich, J., Gomez, F. P., Benet, M., Farrero, E., Basagana, X., Gayete, A., Pare, C., Freixa, X., Ferrer, J., Ferrer, A., Roca, J., Galdiz, J. B., Sauleda, J., Monso, E., Gea, J., Barbera, J. A., Agusti, A., Anto, J. M., & on behalf of the PAC-COPD Study Group. (2011). Identification and prospective validation of clinically relevant chronic obstructive pulmonary disease (COPD) subtypes. Thorax. https://doi.org/10.1136/thx.2010.154484

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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.