Does a 'reverse' atopic march exist?
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Published on: July 5, 2011
G Barberio1, G B Pajno, D Vita
1Department of Pediatrics, Allergy Unit, University of Messina, Italy.
Insights
The atopic march, a common allergy progression, may not always start with atopic dermatitis. This study found children with asthma alone can develop atopic dermatitis later, challenging the traditional pathway.
Area of Science:
- Allergy and Immunology
- Pediatric Respiratory Medicine
- Dermatology
Background:
- The classical atopic march describes a progression from atopic dermatitis to asthma.
- This established pathway has been increasingly questioned in recent research.
Purpose of the Study:
- To investigate the onset of atopic dermatitis in children who initially presented with asthma alone.
- To evaluate the characteristics of children developing atopic dermatitis after a baseline diagnosis of asthma.
Main Methods:
- A prospective observational study followed 745 children (6-9 years) with asthma but no prior atopic dermatitis or food allergy.
- Children were monitored for 9 years, with 692 completing the observation period.
- Retrospective analysis compared demographic, familial, and sensitization profiles of children who developed atopic dermatitis versus those who did not.
Main Results:
- 20% of children initially diagnosed with asthma alone developed atopic dermatitis over the 9-year follow-up.
- No significant baseline differences in demographics or family history were found between groups.
- Children who developed atopic dermatitis showed a higher proportion of single sensitization to mites and lower polysensitization compared to controls.
Conclusions:
- The development of atopic dermatitis can occur in children with asthma as the initial allergic manifestation.
- These findings challenge the rigid, classical paradigm of the atopic march.
- Allergic disease progression may be more variable than previously understood.
Abstract:
The classical description of the atopic march usually refers to the progression from atopic dermatitis towards asthma, but this pathway has been questioned. We assessed in a prospective observation the possible onset of atopic dermatitis in children with asthma alone at baseline, and evaluated retrospectively their characteristics. Seven hundred and forty-five children (360 male, 6-9 years of age) with asthma alone, without food allergy or atopic dermatitis, were followed-up with regular visits for 9 years. 692 children completed the 9-year observation, and 20% of them were found to have developed atopic dermatitis at 9 years. Comparing retrospectively the children who developed AD with the remaining, no significant difference existed at baseline concerning the demographic characteristics and family history. There was a significantly higher proportion ( chi2 = 0.01) of subjects with single sensitization to mites and a significantly lower proportion of polysensitized subjects ( chi2 = 0.01) within the children who developed AD. Sensitization to foods appeared in 9% of children who developed AD and in 3.8% in the other children (NS). According to these observations, the development of a particular allergic disease does not necessarily follow the classical paradigm of the atopic march.
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