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Published on: August 7, 2017
Measuring inflammation in paediatric severe asthma: biomarkers in clinical practice
Amelia Licari1,2, Sara Manti3,2, Riccardo Castagnoli1
1Pediatric Clinic, Fondazione IRCCS Policlinico San Matteo, University of Pavia, Pavia, Italy.
Insights
Identifying biomarkers for severe asthma in children is crucial for personalized treatment. Current non-invasive markers primarily detect type 2 inflammation, but non-type 2 asthma requires further research.
Area of Science:
- Pediatric Pulmonology
- Immunology
- Biomarker Discovery
Background:
- Severe asthma in children is heterogeneous, with diverse phenotypes and endotypes.
- Personalized therapy requires identifying non-invasive biomarkers for treatment response prediction.
- Current biomarkers mainly indicate type 2 inflammation, leaving non-type 2 asthma diagnosed by exclusion.
Purpose of the Study:
- To review recent evidence on biomarkers for severe pediatric asthma.
- To discuss the clinical implementation of these biomarkers for patient identification and treatment guidance.
Main Methods:
- Literature review of current research on severe asthma biomarkers in children.
- Analysis of non-invasive biomarkers reflecting airway inflammation (eosinophils, IgE, nitric oxide).
- Discussion of clinical utility in guiding treatment decisions and patient stratification.
Main Results:
- Established biomarkers like blood/sputum eosinophils, serum IgE, and exhaled nitric oxide are key indicators of type 2 inflammation.
- The identification and understanding of biomarkers for non-type 2 asthma remain limited.
- Clinical implementation strategies for existing biomarkers are discussed.
Conclusions:
- Biomarkers are essential for managing heterogeneous severe asthma in children.
- Further research is needed to identify reliable biomarkers for non-type 2 pediatric asthma.
- Clinical practice can benefit from current biomarkers to guide personalized therapeutic approaches.
Abstract:
Severe asthma in children is a highly heterogeneous disorder, encompassing different clinical characteristics (phenotypes) and immunopathological pathways (endotypes). Research is focusing on the identification of noninvasive biomarkers able to predict treatment response and assist in designing personalised therapies for severe asthma. Blood and sputum eosinophils, serum IgE and exhaled nitric oxide fraction mostly reflect type 2 airway inflammation in children. However, in the absence of available point-of-care biomarkers, the diagnosis of non-type 2 asthma is still reached by exclusion. In this review, we present the most recent evidence on biomarkers for severe asthma and discuss their implementation in clinical practice. We address the methods for guiding treatment decisions and patient identification, focusing on the paediatric age group.
Key Points:
Severe asthma in children is a highly heterogeneous disorder, encompassing different clinical characteristics (phenotypes) and immunopathological pathways (endotypes).Research is focusing on the identification of noninvasive biomarkers able to predict treatment response and assist in designing personalised therapies for severe asthma.Blood and sputum eosinophils, serum IgE and exhaled nitric oxide fraction mostly reflect type 2 airway inflammation in children. However, knowledge regarding non-type 2 inflammation and related biomarkers is still lacking.
Educational Aims:
To summarise the most recent evidence on biomarkers for severe asthma in children.To discuss their implementation in clinical practice through guiding patient identification and treatment decisions.
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