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Lack of eosinophilia can predict remission in wheezy infants?
J Just1, N Nicoloyanis, M Chauvin
1Centre de l'Asthme et des Allergies, Groupe Hospitalier Trousseau-La Roche Guyon, Assistance Publique, Hôpitaux de Paris, Université Pierre et Marie Curie, Paris, France. jocelyne.just@trs.aphp.fr
Insights
Lack of eosinophilia in wheezy infants can predict remission of childhood wheezing. This finding helps identify infants at lower risk for persistent respiratory symptoms into later childhood.
Area of Science:
- Pediatric Allergy and Immunology
- Respiratory Medicine
- Clinical Pediatrics
Background:
- Infant wheezing is a risk factor for adult asthma.
- Atopy history increases wheezing persistence, but relative importance is unclear.
Purpose of the Study:
- Determine critical thresholds for atopy markers predicting childhood wheezing persistence.
- Rank biological and clinical markers by association strength with wheezing persistence.
Main Methods:
- Cohort of infants (<30 months) with recurrent wheezing.
- Assessed respiratory symptoms and atopy markers.
- Re-evaluated wheezing remission at 6 years of age.
Main Results:
- Wheezing persisted in 27% of 219 subjects at age 6.
- Critical thresholds: blood eosinophilia count >= 470/mm(3) and total serum IgE level >= 45 IU/mL.
- Eosinophilia was the main predictor of wheezing remission (91% discrimination).
Conclusions:
- Lack of eosinophilia in wheezy infants (without infection) predicts remission in most cases.
- This marker aids in identifying infants likely to outgrow wheezing.
Background:
Early wheezing in infants is a potential risk factor for persistence of asthma into adulthood. Moreover, a personal or familial history of atopy are risk factors associated with persistence of pre-existing wheezing during childhood. However, their relative importance remains unclear.
Objectives:
Firstly to determine the critical thresholds of common biological markers of atopy in wheezy infants associated with persistence of wheezing into childhood and secondly to rank these biological markers together with clinical parameters according to the strength of their association with wheezing persistence.
Methods:
A cohort of infants less than 30 months old with recurrent wheezing was established in order to assess severity of respiratory symptoms and to look for the presence of atopy. At the age of 6 years, they were re-evaluated regarding remission of wheezing over the previous 12-months period.
Results:
Data were available for 219 subjects. In 27% of them, wheezing persisted at 6 years of age. Critical biological thresholds associated with the risk of wheezing persistence were: (1) a blood eosinophilia count >or=470/mm(3) (defining eosinophilia), and (2) a total serum IgE level >or=45 IU/mL (defining elevated IgE) during infancy. A multiple component factorial analysis identified a dimension associating eosinophilia, elevated IgE and allergic sensitization on the one hand with persistent wheezing at 6 years of age on the other (lambda=0.15). According to a segmentation analysis, the main discriminative parameter of wheezing persistence was eosinophilia. Thus a lack of eosinophilia alone could account for 91% of infants in remission, and when combined with absence of allergic sensitization, remission was correctly discriminated in 96.9% of the study population.
Conclusion:
Our data strongly suggest that the lack of eosinophilia in wheezy infants without ongoing infection could predict future remission of wheezing in a large majority of cases.
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