Real-world phenotyping and risk assessment of childhood asthma burden using national registries

Kjell Erik Julius Håkansson*, Nada Alabdulkarim, Silvia Cabrera Guerrero, Vibeke Backer, Charlotte Suppli Ulrik, Deepa Rastogi

*Corresponding author af dette arbejde

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningpeer review

1 Citationer (Scopus)
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Abstract

Background
Phenotype classification contributes to risk assessment of asthma. Previous studies have applied this concept primarily to adult populations and in the setting of research protocol assessments which may not be applicable to clinical settings.
Objective
Exploring the value of routinely collected clinical data for phenotype classification and risk assessment of childhood asthma.
Methods
Using hospital and laboratory data, 29,851 children in a Danish nationwide database aged 2–17 years with ICS-treated asthma in 2015 followed for two years (730 days) were classified to have T2 (elevated blood eosinophils (>300 cells/μL) and/or elevated total- or specific-IgE), and/or non-T2 risk factors (in utero tobacco exposure and/or severe viral infections). Logistic regression was applied to quantify associations of risk factors with asthma severity, control, and exacerbation risk.
Results
In a complete case analysis, 85.8 % children had at least one T2 risk factor and 29.3 % had mixed T2/non-T2 risk factors. Elevated blood eosinophils and total/specific IgE were associated with exacerbations (ORs 1.55 (1.38–1.73) and 1.41 (1.20–1.66) and higher asthma severity (1.42 (1.24–1.63) and 1.31 (1.08–1.60)), respectively.
Dose-dependency was observed between blood eosinophil counts, total IgE levels, and risk of adverse outcomes. Furthermore, accumulation of risk factors demonstrated an increasing risk, with children with all four risk factors having a high risk of any adverse asthma-related outcome (OR 3.13 (2.03–4.82)
Conclusion
Asthma phenotypic markers defined in research protocols can be reliably applied in real-world settings by utilizing data collected during routine clinical care and enable better classification of risk of adverse asthma outcomes.
OriginalsprogEngelsk
Artikelnummer107808
TidsskriftRespiratory Medicine
Vol/bind234
Antal sider9
ISSN0954-6111
DOI
StatusUdgivet - 2024

Bibliografisk note

Funding Information:
This work was funded by B\u00F8rnelungefonden, the Respiratory Research Unit, Hvidovre Hospital, and an unrestricted research grant from Sanofi Genyzme.

Publisher Copyright:
© 2024

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