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Biomarkers for Severe Asthma: Lessons From Longitudinal Cohort Studies
Youngsoo Lee1, Quang Luu Quoc1,2, Hae Sim Park1,3
1Department of Allergy and Clinical Immunology, Ajou University School of Medicine, Suwon, Korea.
Severe asthma is complex, with advances focusing on type 2 inflammation. Research is expanding to understand non-type 2 asthma phenotypes and discover new biomarkers for better treatment outcomes.
Area of Science:
- Pulmonology
- Immunology
- Biomarker Discovery
Background:
- Severe asthma (SA) is a complex, heterogeneous respiratory disease.
- Advances in understanding SA pathophysiology have led to targeted biologic therapies, primarily for type 2-high asthma.
- Type 2 inflammatory biomarkers (e.g., IgE, IL-4, IL-5, IL-13, eosinophils, FeNO) are crucial for diagnosis and predicting treatment response.
Purpose of the Study:
- To explore the heterogeneity of severe asthma, including type 2-low and mixed phenotypes.
- To investigate novel biomarkers for severe asthma.
- To highlight the value of real-world cohort studies in addressing unmet needs in SA research.
Main Methods:
- Review of cross-sectional studies, randomized clinical trials, and real-world cohort studies.
- Analysis of type 2 inflammatory biomarkers and their correlation with SA characteristics.
- Investigation into non-type 2 asthma phenotypes.
Main Results:
- Type 2 biomarkers are established predictors of inflammation, symptoms, exacerbations, and treatment efficacy in SA.
- Type 2-low and mixed asthma phenotypes contribute significantly to SA heterogeneity.
- Real-world cohort studies are emerging as valuable tools for SA research.
Conclusions:
- Understanding SA heterogeneity, including non-type 2 phenotypes, is critical.
- Continued research into novel biomarkers is necessary to address the unmet needs in severe asthma management.
- Real-world evidence complements clinical trials in advancing SA knowledge.
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