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Published on: September 26, 2019
Skin biomarkers predict development of atopic dermatitis in infancy
Maria Rasmussen Rinnov1, Anne-Sofie Halling1,2, Trine Gerner1
1Department of Dermatology and Allergy, Herlev and Gentofte Hospital, University of Copenhagen, Hellerup, Denmark.
Infant lipid alterations, including lower phytosphingosine, predict atopic dermatitis (AD) risk. Specific sphingoid base chain lengths and higher TARC/CCL17 also indicate future AD development.
Area of Science:
- Dermatology
- Biochemistry
- Pediatrics
Background:
- Pediatric atopic dermatitis (AD) lacks predictive biomarkers for early onset.
- Understanding early skin barrier differences is crucial for predicting AD.
Purpose of the Study:
- To identify early biomarkers predicting the onset of pediatric atopic dermatitis (AD).
- To investigate skin barrier components in infants before AD manifestation.
Main Methods:
- Analysis of tape strips from infants at 2 months of age.
- Measurement of Natural moisturizing factor (NMF), corneocyte surface, cytokines, free sphingoid bases (SBs), and ceramides.
- Utilized liquid chromatography, atomic force microscopy, and mass spectrometry.
Main Results:
- Significantly lower phytosphingosine ([P]) levels observed in infants who developed AD (240 pmol/mg vs. 540 pmol/mg).
- Differences noted in sphingoid base chain lengths (C17, C18, C20) between groups.
- Phytosphingosine achieved 75.6% prediction accuracy; a lipid ratio combination reached 89.4%.
Conclusions:
- Altered lipid levels and sphingoid base chain lengths in infants are associated with later AD development.
- Elevated TARC/CCL17 levels were also observed in infants who developed AD.
- These findings offer potential biomarkers for predicting pediatric atopic dermatitis.
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