Abstract

The recent Lancet commission has highlighted that “asthma” should be used to describe a clinical syndrome of wheeze, breathlessness, chest tightness, and sometimes cough. The next step is to deconstruct the airway into components of fixed and variable airflow obstruction, inflammation, infection and altered cough reflex, setting the airway disease in the context of extra-pulmonary co-morbidities and social and environmental factors. The emphasis is always on delineating treatable traits, including variable airflow obstruction caused by airway smooth muscle constriction (treated with short- and long-acting β-2 agonists), eosinophilic airway inflammation (treated with inhaled corticosteroids) and chronic bacterial infection (treated with antibiotics with benefit if it is driving the disease). It is also important not to over-treat the untreatable, such as fixed airflow obstruction. These can all be determined using simple, non-invasive tests such as spirometry before and after acute administration of a bronchodilator (reversible airflow obstruction); peripheral blood eosinophil count, induced sputum, exhaled nitric oxide (airway eosinophilia); and sputum or cough swab culture (bacterial infection). Additionally, the pathophysiology of risk domains must be considered: these are risk of an asthma attack, risk of poor airway growth, and in pre-school children, risk of progression to eosinophilic school age asthma. Phenotyping the airway will allow more precise diagnosis and targeted treatment, but it is important to move to endotypes, especially in the era of increasing numbers of biologicals. Advances in -omics technology allow delineation of pathways, which will be particularly important in TH2 low eosinophilic asthma, and also pauci-inflammatory disease. It is very important to appreciate the difficulties of cluster analysis; a patient may have eosinophilic airway disease because of a steroid resistant endotype, because of non-adherence to basic treatment, and a surge in environmental allergen burden. Sophisticated –omics approaches will be reviewed in this manuscript, but currently they are not being used in clinical practice. However, even while they are being evaluated, management of the asthmas can and should be improved by considering the pathophysiologies of the different airway diseases lumped under that umbrella term, using simple, non-invasive tests which are readily available, and treating accordingly.

Highlights

  • APPROACHING AIRWAYS DISEASEThe recent Lancet Asthma Commission [1] was predicated on the assumption that the term “asthma” was no more a diagnosis than is “arthritis” or “anemia.” It is an umbrella term that should be used to describe a constellation of clinical symptoms, namely wheeze, breathlessness, chest tightness and cough, and should be followed by the question “what sort of asthma is this?” Dissecting out the individual asthmas is increasingly important as novel biologicals with different modes of action are increasingly being deployed

  • Is there any other chronic condition in which simple tests are available, but are routinely not performed before committing a child to long term treatment? We should use our knowledge of the pathophysiology of asthma to phenotype the airway, even in young children, focusing on the treatable traits

  • We have shown that the prescription of ICS in primary ciliary dyskinesia (PCD) is haphazard and bears no relationship to any marker of atopic sensitization or airway eosinophilia [96]

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Summary

Andrew Bush*

Departments of Paediatrics and Paediatric Respiratory Medicine, Royal Brompton Harefield NHS Foundation Trust and Imperial College, London, United Kingdom. It is important not to over-treat the untreatable, such as fixed airflow obstruction These can all be determined using simple, non-invasive tests such as spirometry before and after acute administration of a bronchodilator (reversible airflow obstruction); peripheral blood eosinophil count, induced sputum, exhaled nitric oxide (airway eosinophilia); and sputum or cough swab culture (bacterial infection). Sophisticated –omics approaches will be reviewed in this manuscript, but currently they are not being used in clinical practice. Even while they are being evaluated, management of the asthmas can and should be improved by considering the pathophysiologies of the different airway diseases lumped under that umbrella term, using simple, non-invasive tests which are readily available, and treating

AIRWAYS DISEASE
AIRWAY DISEASE
Treatable Trait of Airway Eosinophilia
Fixed and Variable Airflow Obstruction
Airway Infection and the Asthmas
Asthma Attacks
Adverse Trajectories of Lung Function
Risk of Progressive Disease
AIRWAY PHENOTYPING
Endoyping Asthma With Omics Technology
Omics Technology
Generating Studies
Endotypes of Inflammation
Airflow Limitation
Eosinophilic Airway Disease
IN PRACTICE?
Findings
SUMMARY AND CONCLUSIONS

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