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The Utility of Nasal Challenges to Phenotype Asthma Patients

期刊

出版社

MDPI
DOI: 10.3390/ijms23094838

关键词

asthma phenotypes; nasal challenge; biomarker; allergic asthma; NSAID-exacerbated respiratory disease

资金

  1. Instituto de Salud Carlos III (ISCIII) of the Spanish Ministry of Science and Competitiveness [PI20/01715]
  2. European Regional Development Fund
  3. Regional Ministry of Education of Andalucia [P20_00405]
  4. Rio Hortega contract by ISCIII [CM20/00160]
  5. Juan Rodes contract by ISCIII
  6. ISCIII
  7. European Regional Development Fund through its program of Redes de Investigacion Cooperativa Orientadas al Resultado en Salud (RICORS): Enfermedades Inflamatorias [RD21/0002/0008]

向作者/读者索取更多资源

Asthma is a heterogeneous disease in terms of both phenotype and response to therapy. Currently available biomarkers have limitations in asthma phenotyping. The united airway concept has been widely applied in patient management and treatment, but its diagnostic implications have been less explored.
Asthma is a heterogeneous disease in terms of both phenotype and response to therapy. Therefore, there is a great need for clinically applicable tools allowing for improved patient classification, and selection for specific management approaches. Some interventions are highly helpful in selected patients (e.g., allergen immunotherapy or aspirin desensitization), but they are costly and/or difficult to implement. Currently available biomarkers measurable in peripheral blood or exhaled air display many limitations for asthma phenotyping and cannot identify properly the specific triggers of the disease (e.g., aeroallergens or NSAID). The united airway concept illustrates the relevant epidemiological and pathophysiological links between the upper and lower airways. This concept has been largely applied to patient management and treatment, but its diagnostic implications have been less often explored. Of note, a recent document by the European Academy of Allergy and Clinical Immunology proposes the use of nasal allergen challenge to confirm the diagnosis of allergic asthma. Similarly, the nasal challenge with lysine acetylsalicylate (L-ASA) can be used to identify aspirin-sensitive asthma patients. In this review, we will summarize the main features of allergic asthma and aspirin-exacerbated respiratory disease and will discuss the methodology of nasal allergen and L-ASA challenges with a focus on their capacity to phenotype the inflammatory disease affecting both the upper and lower airways.

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