4.5 Article

Biomarkers in asthma in the context of atopic dermatitis in young children

Journal

PEDIATRIC ALLERGY AND IMMUNOLOGY
Volume 33, Issue 7, Pages -

Publisher

WILEY
DOI: 10.1111/pai.13823

Keywords

asthma; atopic dermatitis; biomarkers; CCL18; NMF; sensitization; TSLP

Funding

  1. Region of Southern Denmark
  2. University of Southern Denmark
  3. Gangstedfonden
  4. Kongelig Hofbuntmager Aage Bangs Fond
  5. Aase og Ejnar Danielsens Fond
  6. A.P. Moller Foundation for the Advancement of Medical Science
  7. Odense University Hospital Free Research Fund
  8. Ingemann O. Bucks Legat
  9. Hans Christian Andersen Children's Hospital Research Unit, Odense University Hospital

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The clinical and molecular characteristics of an AD+asthma phenotype were investigated and compared with AD, asthma, and control groups. The study found an increased number of IgE sensitizations and elevated levels of Pro-Th-2 cytokines in the AD+asthma group. NMF levels were decreased in AD. These findings suggest potential biomarkers and provide insights into the pathogenesis of AD+asthma.
Background Diverse pathways stemming from a history of atopic dermatitis (AD) might modulate different biomarkers associated with the development of asthma. Biomarkers associated with AD and asthma separately have been investigated, but none have characterized a combined AD+asthma phenotype. We investigated the clinical and molecular characteristics associated with an AD+asthma phenotype compared with AD, asthma and controls. Methods From a prospective birth cohort and the outpatient allergy clinic, we included four groups of 6-12-year-old children: (1) healthy controls (2) previous, current, or present AD without asthma, (3) previous, current, or present AD and current asthma and (4) current asthma without AD. We performed clinical examinations and interviews and measured serum IgE, natural moisturizing factors (NMF), and plasma cytokine levels. Results We found an increased number of IgE sensitizations in AD+asthma, prominent after stratifying for food allergens (p < .05). Pro-Th-2 cytokines CCL18, TSLP, and Eotaxin-3 were elevated in AD+asthma, though not significantly higher than asthma, and elevated in asthma compared with controls. NMF levels were decreased in AD compared with asthma and control groups (p = .019, p < .001, respectively). NMF levels correlated negatively to sensitization (p = .026), though nonsignificant with only the patient groups. Conclusion Our results indicate that Th-2 cytokines and increased number of sensitizations are associated with AD + asthma phenotypes compared with AD alone and that skin barrier impairment as well as decreased airway epithelial integrity may play a role in sensitization and immune modulation. Our findings suggest candidate biomarkers that should be further explored for their functional roles and prognostic potential.

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