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Association between skin barrier development and early-onset atopic dermatitis: A longitudinal birth cohort study
John Chittock1, Linda Kay1, Kirsty Brown1
1Sheffield Dermatology Research, Division of Clinical Medicine, University of Sheffield Medical School, Sheffield, United Kingdom.
Insights
Infant skin barrier development shows subtle differences, but genetic factors and early biomarkers like reduced natural moisturizing factor are key indicators for atopic dermatitis (AD) risk. This study highlights potential for improved early AD risk assessment.
Area of Science:
- Dermatology
- Genetics
- Pediatrics
Background:
- Atopic dermatitis (AD) is a common infant diagnosis, but the role of skin barrier development in its onset is unclear.
- Understanding early skin barrier maturation is crucial for identifying infants at risk of developing AD.
Purpose of the Study:
- To assess the feasibility of remote skin testing from birth.
- To monitor skin barrier maturation and its association with AD diagnosis by 12 months.
- To investigate genetic predispositions and early biomarkers for AD.
Main Methods:
- Biophysical testing and infrared spectroscopy were performed in homes and maternity wards.
- Tape stripping analyzed desquamatory protease and natural moisturizing factor (NMF).
- Screening for common European filaggrin risk alleles was conducted.
Main Results:
- Subtle differences in skin barrier development were observed between infant subgroups.
- Filaggrin risk alleles strongly correlated with early-onset AD, reducing NMF and water content.
- Reduced NMF, higher lipid/protein ratio, and lower protease activity at birth, along with family history, predicted AD.
Conclusions:
- Skin barrier dysfunction in AD appears inherent rather than acquired.
- A combination of tests at birth can potentially improve early AD risk evaluation.
- Remote monitoring and a portfolio of tests show promise for community-based AD risk assessment.
Background:
A diagnosis of atopic dermatitis (AD) is common during infancy; however, it is unclear whether differential skin barrier development defines this period and signals disease onset in predisposed individuals.
Objective:
We sought to study (NCT03143504) and assess the feasibility of remote skin testing from birth to monitor skin barrier maturation and model association with an AD diagnosis by age 12 months.
Methods:
Biophysical testing and infrared spectroscopy were conducted at the maternity ward and family home. Tape stripping collected samples for desquamatory protease and natural moisturizing factor analysis. The 4 common European filaggrin risk alleles were screened.
Results:
A total of 128 infants completed the study, with 20% developing mild disease. Significant changes in permeability barrier function, desquamatory protease activity, and molecular composition assessed spectroscopically were observed longitudinally, but only subtle evidence of differential skin barrier development was noted between infant subgroups. Common filaggrin risk alleles were strongly associated with early-onset disease and conferred a significant reduction in natural moisturizing factor and water content by age 4 weeks. Accounting for a family history of atopy, these parameters alongside a greater lipid/protein ratio and reduced chymotrypsin-like activity at birth were associated with AD. Measured in ambient conditions, transepidermal water loss did not signal disease risk at any stage.
Conclusions:
Skin barrier dysfunction lacked an acquired modality but was considered proportional to cohort severity and suggests that a portfolio of tests used in a community setting has the potential to improve current AD risk evaluations from birth.
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