The notion that severe asthma is a heterogeneous condition that may benefit from phenotyping is becoming more widely accepted.1
No present system of subgrouping has achieved all requirements of a true phenotype.
Phenotyping patients with asthma has become a part of the diagnostic workup for patients who do not respond satisfactorily to standard therapy with inhaled corticosteroids (ICS).1,3,4
The notion of distinct phenotypes in severe asthma is gaining acceptance.
Further identification of asthma phenotypes is being explored for disease management.
Emerging data from large cohorts support heterogeneity in severe asthma, with increasing acceptance of the presence of distinct phenotypes4
Phenotyping may potentially allow for better understanding of disease heterogeneity and facilitate individualization of patient management by grouping patients with common clinical features6
The future of disease management may be impacted by identification of causal pathways as they apply to the different asthma phenotypes5
However, the stability of phenotypes identified in cluster analyses and their use in predicting long-term outcomes and responses to therapy is still uncertain6
May allow for better understanding of disease heterogeneity and facilitate individualization of patient management by grouping patients with common clinical features2
A goal of phenotyping is to individualize and optimize therapy1
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Wenzel SE. Asthma phenotypes: the evolution from clinical to molecular approaches.
de Groot JC, ten Brinke A, Bel EHD. Management of the patient with eosinophilic asthma: a new era begins.
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Wenzel S. Severe asthma: from characteristics to phenotypes to endotypes.
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Middleton's Allergy Principles and Practice.
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Bourdin A, Molinari N, Vachier I, et al. Prognostic value of of cluster analysis of severe asthma phenotypes.
J Allergy Clin Immunol.