- Letter to the Editor
- Open Access
Asthma-COPD overlap is not a homogeneous disorder: further supporting data
© The Author(s). 2017
- Received: 23 June 2017
- Accepted: 17 October 2017
- Published: 2 November 2017
Asthma-COPD ovelap (ACO) is an umbrella term that encompasses patients with COPD and eosinophilic inflammation (e-COPD) and smoking asthmatics with non-fully reversible airflow obstruction (SA). We compared the clinical characteristics and the inflammatory profile of e-COPD and SA. Patients classified as e-COPD were older and more often male and showed significantly impaired pulmonary function (likely explained by a heavier smoking habit). On the contrary, SA had more atopic features, more reversibility of airflow obstruction and higher IgE levels. The concentrations of IL-5, IL-13, IL-8, IL-6, TNF-α, IL17 in serum were similar between the 2 groups. However, Th2-related biomarkers (periostin, FeNO and blood eosinophils) shower higher median values in e-COPD patients. Our findings reinforce the notion that ACO is a heterogeneous disorder and, as a consequence, it might be unacceptable to offer the same treatment for two related but different conditions.
- Asthma-COPD overlap
We have read with great interest the letter by Kolsum et al.  and we fully agree that eosinophilic COPD (e-COPD) patients have distinct characteristics compared to smoking asthmatics (SA) who develop non-fully reversible airflow obstruction. Both entities are commonly encompassed under an umbrella term , the so-called Asthma-COPD overlap (ACO), but, in the age of personalized medicine , it might be unacceptable to offer the same treatment for two related but different conditions. Studies that focus on identifying ACO’s phenotypes are scarce, but Lange et al. found that individuals with ACO and asthma onset before the age of 40 years have better prognosis than those whose asthma starts after this age . On the other hand, given that asthma and COPD are themselves heterogeneous diseases, one could argue whether it is necessary to define their overlap as a new entity. All these problems could be sorted out by identifying endotypes of obstructive lung disease (OLD) that would allow a personalized approach to therapy. In this regard, we have recently published a study that postulated the extinction of ACO and the use of a Th2 inflammation biomarker to differentiate a pooled population of patients with OLD . With this letter, we would like to provide additional information to support the differentiation between e-COPD and SA.
We have performed a cross-sectional, observational, multicenter study carried out in 23 out-patient clinics from tertiary hospitals in Spain. The details of the design are described elsewhere . Two hundred and ninety-two patients with OLD were included in the study: 94 non-smoking asthmatics, 89 non-eosinophilic COPD, 44 SA and 65 e-COPD. All investigators were asked to prospectively recruit 12 consecutive eligible patients with OLD from their clinics.
Patients were labelled as SA if they had been previously diagnosed with asthma according to GINA guidelines  and, after having smoked >20 pack-years, they subsequently developed non-fully reversible airflow obstruction (FEV1/FVC <70% post-bronchodilator). The diagnosis of e-COPD was made in patients who were previously diagnosed with COPD according to GOLD recommendations , in the absence of a clinical suspicion for asthma and in the presence of a blood eosinophil count >200 eosinophils/μl.
Demographics, clinical and functional characteristics of patients
Number of subjects
Gender (% female)
Age of onset (yrs)
Patients with nocturnal symptoms (%)
-Arterial hypertension (%)
-Ischemic heart disease (%)
-Heart failure (%)
-Psychiatric disorders (8%)
-Gastro-esophageal Reflux (%)
Prebd FEV1d (%)
112 (4, 1340)
These results are well in accordance with those found by Kolsum et al., and the most remarkable difference is that we were unable to observe any difference between groups in the exacerbation rate in the 12 months prior to study entry, while they found AS to be more prone to suffer exacerbations. To explain this discordance, we must take into account that our patients were fairly well-controlled as assessed by the CAT and ACT questionnaires and the low exacerbation rate.
Differences in the inflammatory profile between the 2 groups
Smoking asthmatics n = 44
e-COPD n = 65
Blood Eos (cels/μl)
It has been largely debated whether asthma and COPD are distinct entities generated by different mechanisms  or, on the contrary, they are in fact expressions of one basic disease in which the combined endogenous (host) and exogenous (environmental) factors shape the patient’s clinical profile . Irrespective of that, a current perspective of classification and therapeutic management of OLD patients should take into account the growing knowledge on molecular pathways that has allowed the development of novel therapeutic strategies that target specific components of the underlying inflammatory process. Previous attempts to define ACO [2, 6, 7, 13] do not consider the biological heterogeneity that we, and Kolsum et al., have found, which might potentially lead to inadequate therapeutic approaches. Any useful definition of ACO should offer guidance to make therapeutic decisions, particularly to effectively select who of them can benefit from inhaled corticosteroids treatment (or even anti-Th2 biological drugs in the near future).
In conclusion, our findings reinforce the notion that ACO is a heterogeneous disorder. In fact, OLD is heterogeneous and classical diagnostic categories are unable to fully explain the great complexity of the underlying inflammatory process that ultimately determines the response to treatment. Therefore, we must advance step by step towards a more personalized medicine.
CHACOS collaboration group: Amanda Iglesias1, Natividad de las Cuevas2, Juan Jose Soler-Cataluña3,1, Jose Luis Izquierdo4, Jose Luis López-Campos5,1, Carmen Calero6, Vicente Plaza6,1, Marc Miravitlles7,1, Alfons Torrego6, Eva Martínez Moragón8, Joan B Soriano9, Antolin Lopez Viña10 and Irina Bobolea11.
All of them gave the authors permission to acknowledge.
1. CIBER de Enfermedades Respiratorias (CIBERES). Instituto de Salud Carlos III, Madrid
2. Department of Allergy, hospital 12 de Octubre, Madrid, Spain
3. Department of Respiratory Medicine, hospital Arnau de Vilanova, Valencia, Spain
4. Department of Respiratory Medicine, hospital Universitario de Guadalajara, Guadalajara, Spain
5. Department of Respiratory Medicine, Hospital Virgen del Rocío, Sevilla, Spain.
6. Department of Respiratory Medicine, Hospital de la Santa Creu y Sant Pau, Barcelona; Institut d’Investigació Biomédica Sant Pau (IIB Sant Pau); Universitat Autònoma de Barcelona, Department of Medicine, Barcelona, Spain.
7. Department of Respiratory Medicine, Hospital Universitari Vall d’Hebron, Barcelona, Spain.
8. Department of Respiratory Medicine, Hospital Dr. Peset, Valencia, Spain.
9. Instituto de Investigación Hospital de la Princesa, Universidad Autónoma de Madrid, Madrid, Spain.
10. Department of Respiratory Medicine, Hospital Puerta de Hierro, Madrid, Spain.
11. Servei de Pneumologia i Alergia. Hospital Clinic. Barcelona.
The project was endorsed by the COPD and Asthma Research Board (PII de EPOC y asma) of the Spanish Society of Pneumology and Thoracic Surgery (SEPAR). The project was partially funded by the Fondo de Investigaciones Sanitarias, Instituto de Salud Carlos III, Ministerio de Economia y Competitividad (FIS 15/01263) and by an unrestricted grant from Chiesi España S.A.U.
Availability of data and materials
The datasets used and/or analysed during the current study are available from the corresponding author on reasonable request.
LPLL and BC made substantial contributions to conception and design of the study, and analysis and interpretation of data. They have both been involved in drafting the manuscript and revising it critically for important intellectual content. Both authors have read and approved the final manuscript.
Ethics approval and consent to participate
The data presented here were extracted from a cross-sectional, observational, multicenter study carried out in 23 out-patient clinics from tertiary hospitals in Spain run by expert respiratory physicians. All participants gave a signed informed consent. The study was approved by the Research Ethics Committee of the Balearic Islands (Cod: IB2499/15). Additionally, an independent Ethics committee or institutional review board for each study centre approved the final protocol.
Consent for publication
A consent form will be be made available to the Editor if requested.
The authors declare that they have no competing interests.
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Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
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