Related Experiment Video
Updated: Aug 25, 2026

Noninvasive Sampling of Mucosal Lining Fluid for the Quantification of In Vivo Upper Airway Immune-mediator Levels
Published on: August 7, 2017
Salivary OMICS factors associated with atopic dermatitis in early infancy
Nora Alomeir1, Ellen Chinchilli2, Chloe Terio3
1Eastman Institute for Oral Health, University of Rochester Medical Center, Rochester, New York, USA.
Insights
Early detection of atopic dermatitis (AD) in infants is possible using noninvasive salivary biomarkers. Hormonal and cytokine levels, along with oral microbiome profiles, can indicate infants at risk for developing AD.
Area of Science:
- Pediatric Allergy and Immunology
- Microbiome Research
- Biomarker Discovery
Background:
- Atopic dermatitis (AD) is a common childhood condition with limited early noninvasive detection methods.
- Identifying infants at risk for AD is crucial for timely intervention and management.
Purpose of the Study:
- To investigate the association between salivary biomarkers (hormones, cytokines) and oral microbiota with AD onset in infants.
- To determine if these oral biomarkers can serve as early indicators for AD risk.
Main Methods:
- Prospective cohort study of 119 infants from birth to 24 months.
- Saliva samples analyzed for hormones, cytokines (multiplex immunoassays), and microbiome (metagenomic sequencing).
- AD diagnoses confirmed via electronic health records.
Main Results:
- Nearly half of infants developed AD by age 2; peak incidence between 2-4 months.
- Infants with AD showed altered salivary estradiol, progesterone, cortisol, sIL-1ra, IL-9, and IL-1α levels at specific early time points.
- Significant differences in salivary microbiome diversity and reduced abundance of specific bacteria (Bifidobacterium breve, Veillonella atypica) were observed in infants who developed AD.
Conclusions:
- Early-life salivary hormonal, cytokine, and microbiome signatures show potential as noninvasive indicators for identifying infants at risk of early AD onset.
- These findings support the development of novel diagnostic tools for predicting AD in infancy.
Background:
Atopic dermatitis (AD) often develops in early childhood and may persist into adulthood. Noninvasive measures to identify infants at risk for AD are limited. We investigated whether oral biomarkers and oral microbiota are associated with AD onset within the first 2 years of life.
Methods:
In this prospective cohort study, we followed 119 infants residing in Upstate New York from birth to 24 months (2018-2023). AD diagnoses were obtained from electronic health records. Saliva samples were collected at seven time points (1, 2, 4, 6, 12, 18, and 24 months) and analyzed for 5 hormones and 23 cytokines using multiplex immunoassays. Salivary microbiome profiles were characterized via metagenomic sequencing.
Results:
Nearly half (48%) of infants developed AD by age 2, with most cases manifesting by 12 months (42%) and peak incidence occurring between months 2-4. Infants who developed AD by 1 year demonstrated significantly elevated estradiol (p = .007) and progesterone (p = .046) at 1 month, and a significantly lower salivary cortisol level (p = .019) at 6 months. Additionally, these infants exhibited higher sIL-1ra (p = .024) and IL-9 (p = .034) in saliva at 4 months and lower IL-1α (p = .038) at 6 months. Salivary microbiome beta diversity differed significantly at 2 months between infants with and without AD by 1 year (p = .038), with lower differential abundances of Bifidobacterium breve and Veillonella atypica in early infancy prior to AD onset.
Conclusion:
Early-life salivary biomarkers, including hormonal, cytokine, and microbiome signatures, may serve as noninvasive indicators of infants at risk for early AD onset.
Related Concept Videos
Development of the Oral Microbiota
Development of Immunocompetence
The initial cells that migrate from the fetal thymus settle within the skin and epithelial tissues lining the mouth, digestive tract, and in females, the uterus and vagina. These cells, including skin-based dendritic cells, serve as antigen-presenting cells, playing a key role in T cell activation.
Subsequent T...
