Asthma and lower airway disease
Biological clustering supports both “Dutch” and “British” hypotheses of asthma and chronic obstructive pulmonary disease

https://doi.org/10.1016/j.jaci.2014.06.035Get rights and content
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Background

Asthma and chronic obstructive pulmonary disease (COPD) are heterogeneous diseases.

Objective

We sought to determine, in terms of their sputum cellular and mediator profiles, the extent to which they represent distinct or overlapping conditions supporting either the “British” or “Dutch” hypotheses of airway disease pathogenesis.

Methods

We compared the clinical and physiological characteristics and sputum mediators between 86 subjects with severe asthma and 75 with moderate-to-severe COPD. Biological subgroups were determined using factor and cluster analyses on 18 sputum cytokines. The subgroups were validated on independent severe asthma (n = 166) and COPD (n = 58) cohorts. Two techniques were used to assign the validation subjects to subgroups: linear discriminant analysis, or the best identified discriminator (single cytokine) in combination with subject disease status (asthma or COPD).

Results

Discriminant analysis distinguished severe asthma from COPD completely using a combination of clinical and biological variables. Factor and cluster analyses of the sputum cytokine profiles revealed 3 biological clusters: cluster 1: asthma predominant, eosinophilic, high TH2 cytokines; cluster 2: asthma and COPD overlap, neutrophilic; cluster 3: COPD predominant, mixed eosinophilic and neutrophilic. Validation subjects were classified into 3 subgroups using discriminant analysis, or disease status with a binary assessment of sputum IL-1β expression. Sputum cellular and cytokine profiles of the validation subgroups were similar to the subgroups from the test study.

Conclusions

Sputum cytokine profiling can determine distinct and overlapping groups of subjects with asthma and COPD, supporting both the British and Dutch hypotheses. These findings may contribute to improved patient classification to enable stratified medicine.

Key words

Asthma and COPD overlap
cytokines
factor and cluster analyses

Abbreviations used

COPD
Chronic obstructive pulmonary disease
ROC
Receiver operating characteristic
ROC AUC
Area under the receiver operating characteristic curve

Cited by (0)

This study was supported by the Medical Research Council (G0601368), AstraZeneca, MedImmune, and Wellcome Trust Senior Fellowship (WT082265 to C.E.B.). The research was performed in laboratories funded in part by the European Regional Development Fund (grant no. ERDF 05567). This study was also supported in part by the National Institute for Health Research (NIHR) Leicester Respiratory Biomedical Research Unit, UK, and AirPROM (FP7-270194). The views expressed are those of the author(s) and not necessarily those of the National Health Service, the NIHR, or the Department of Health.

Disclosure of potential conflict of interest: M. Bafadhe has received research support from the Medical Research Council and has received travel support (for meeting expenses) from Almirall, Boehringer Ingelheim (BI), and GlaxoSmithKline (GSK). D. Desai has received travel support from BI and Chiesi. S. E. Cohen, P. Newbold, L. Rapley, J. Woods, and R. D. May are employed by and have stock/stock options in MedImmune. P. Rugman is employed by and has stock/stock options in AstraZeneca (AZ). I. D. Pavord reports payments for the recruitment of patients from UHL and personal fees from GSK, AZ, BI, Aerocrine, Boston Scientific, and Novartis. P. R. Burton has received research support from the University of Leicester. C. E. Brightling has received research support and consultancy fees from GSK, MedImmune, BI, Novartis, Roche, and Chiesi; has received travel support from BI, the American Thoracic Society, and Chiesi; and has received travel support from BI, the European Respiratory Society, and the American Thoracic Society. The rest of the authors declare that they have no relevant conflicts of interest.

These authors contributed equally to this work.

Joint senior authors.