Proportional classifications of COPD phenotypes

S. E. Marsh, J. Travers, M. Weatherall, M. V. Williams, S. Aldington, P. M. Shirtcliffe, A. L. Hansell, M. R. Nowitz, A. A. McNaughton, J. B. Soriano, R. W. Beasley

Research output: Contribution to journalArticlepeer-review

189 Citations (Scopus)

Abstract

Background: Chronic obstructive pulmonary disease (COPD) encompasses a group of disorders characterised by the presence of incompletely reversible airflow obstruction with overlapping subsets of different phenotypes including chronic bronchitis, emphysema or asthma. The aim of this study was to determine the proportion of adult subjects aged >50 years within each phenotypic subgroup of COPD, defined as a post-bronchodilator ratio of forced expiratory volume in 1 s/forced vital capacity (FEV1/FVC) <0.7, in accordance with current international guidelines. Methods: Adults aged >50 years derived from a random population-based survey undertook detailed questionnaires, pulmonary function tests and chest CT scans. The proportion of subjects in each of 16 distinct phenotypes was determined based on combinations of chronic bronchitis, emphysema and asthma, with and without incompletely reversible airflow obstruction defined by a post-bronchodilator FEV1/FVC ratio of 0.7. Results: A total of 469 subjects completed the investigative modules, 96 of whom (20.5%) had COPD. Diagrams were constructed to demonstrate the relative proportions of the phenotypic subgroups in subjects with and without COPD. 18/96 subjects with COPD (19%) had the classical phenotypes of chronic bronchitis and/or emphysema but no asthma; asthma was the predominant COPD phenotype, being present in 53/96 (55%). When COPD was defined as a post-bronchodilator FEV1/FVC less than the lower limit of normal, there were one-third fewer subjects with COPD and a smaller proportion without a defined emphysema, chronic bronchitis or asthma phenotype. Conclusion: This study provides proportional classifications of the phenotypic subgroups of COPD which can be used as the basis for further research into the pathogenesis and treatment of this heterogeneous disorder.

Original languageEnglish
Pages (from-to)761-767
Number of pages7
JournalThorax
Volume63
Issue number9
DOIs
Publication statusPublished - Sep 2008
Externally publishedYes

Bibliographical note

Funding Information:
Funding: The study was funded by a research grant from GlaxoSmithKline. ALH is a Wellcome Trust Intermediate Clinical Fellow supported by Grant Number 075883.

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