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

被引:227
作者
Garcia-Aymerich, Judith [1 ,2 ,3 ,4 ]
Gomez, Federico P. [5 ,6 ]
Benet, Marta [1 ,2 ,4 ]
Farrero, Eva [7 ]
Basagana, Xavier [1 ,2 ,4 ]
Gayete, Angel [8 ]
Pare, Carles [9 ]
Freixa, Xavier [9 ]
Ferrer, Jaume [6 ,10 ]
Ferrer, Antoni [2 ,6 ,11 ,16 ]
Roca, Josep [5 ,6 ]
Galdiz, Juan B. [12 ]
Sauleda, Jaume [6 ,13 ,14 ]
Monso, Eduard [6 ,11 ,15 ]
Gea, Joaquim [2 ,3 ,6 ,16 ]
Barbera, Joan A. [5 ,6 ]
Agusti, Alvar [5 ,6 ,14 ]
Anto, Josep M. [1 ,2 ,3 ,4 ]
机构
[1] Ctr Res Environm Epidemiol CREAL, Barcelona 08003, Catalonia, Spain
[2] Hosp del Mar, Municipal Inst Med Res, IMIM, Barcelona, Spain
[3] Univ Pompeu Fabra, Dept Expt & Hlth Sci, Barcelona, Spain
[4] CIBERESP, Barcelona, Spain
[5] Univ Barcelona, Dept Pneumol, Inst Torax, Hosp Clin,IDIBAPS, Barcelona, Spain
[6] CIBER Enfermedades Resp CIBERES, Bunyola, Spain
[7] Hosp Univ Bellvitge, Dept Pneumol, Inst Invest Biomed Bellvitge IDIBEL, Lhospitalet De Llobregat, Spain
[8] Hosp del Mar, IMIM, Dept Radiol, Barcelona, Spain
[9] Univ Barcelona, Dept Cardiol, Hosp Clin, IDIBAPS, Barcelona, Spain
[10] Hosp Gen Univ Vall Hebron, Dept Pneumol, Barcelona, Spain
[11] Hosp Sabadell, Dept Pneumol, Corporacio Parc Tauli, Sabadell, Spain
[12] Hosp Univ Cruces, Dept Pneumol, Upv, Barakaldo, Spain
[13] Hosp Univ Son Dureta, Dept Pneumol, Palma de Mallorca, Spain
[14] Fundacio Caubet Cimera, Bunyola, Spain
[15] Hosp Badalona Germans Trias & Pujol, Dept Pneumol, Badalona, Spain
[16] Hosp del Mar, IMIM, Dept Pneumol, Barcelona, Spain
关键词
QUALITY-OF-LIFE; LUNG-FUNCTION; EXERCISE CAPACITY; CLUSTER-ANALYSIS; DYSPNEA RATINGS; PHENOTYPES; VARIABLES; PROGNOSIS; INDEX;
D O I
10.1136/thx.2010.154484
中图分类号
R56 [呼吸系及胸部疾病];
学科分类号
摘要
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 (FEV1) 38% predicted) and worse performance in most of the respiratory domains of the disease; group 2 (n=125, 69 years) showed milder airflow limitation (FEV1 63% predicted); and group 3 (n=91, 67 years) combined a similarly milder airflow limitation (FEV1 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'.
引用
收藏
页码:430 / 437
页数:8
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