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Prenatal Omega-3 and Omega-6 Polyunsaturated Fatty Acids and Childhood Atopic Dermatitis
Kourtney G Gardner1, Tebeb Gebretsadik2, Terryl J Hartman3
1Division of Allergy, Immunology, and Pulmonology, Vanderbilt University Medical Center, Nashville, Tenn; Department of Medicine, Vanderbilt University Medical Center, Nashville, Tenn.
Insights
Higher prenatal omega-6 (n-6) polyunsaturated fatty acids (PUFAs) were linked to increased atopic dermatitis risk in children. This association was specific to mothers with a history of atopy, suggesting a potential modifiable risk factor.
Area of Science:
- Nutrition Science
- Dermatology
- Pediatrics
Background:
- Atopic dermatitis (AD) is a prevalent childhood skin condition.
- Prenatal nutrition, specifically polyunsaturated fatty acids (PUFAs), may influence AD development.
Purpose of the Study:
- To investigate the association between prenatal omega-6 (n-6) and omega-3 (n-3) PUFA levels and childhood atopic dermatitis.
- To explore potential effect modification by maternal atopic history, smoking, and child sex.
Main Methods:
- Analysis of mother-child dyads from a racially diverse cohort (n=1131).
- Measurement of second-trimester plasma n-3 and n-6 PUFA levels and their ratio.
- Assessment of child atopic dermatitis symptoms at ages 4-6 years using multivariable logistic regression.
Main Results:
- Higher prenatal n-6 PUFA levels were associated with increased odds of childhood atopic dermatitis (aOR: 1.25).
- This association was significant in children of mothers with a history of atopic disease.
- No significant association was found for prenatal n-3 PUFAs or the n-6:n-3 ratio.
Conclusions:
- Elevated second-trimester n-6 PUFAs are linked to atopic dermatitis in children born to mothers with atopy.
- PUFAs may be a modifiable risk factor for atopic dermatitis, especially in genetically predisposed individuals.
Background:
Atopic dermatitis is a common childhood disease, potentially influenced by prenatal nutritional exposures such as polyunsaturated fatty acids (PUFAs).
Objective:
In a racially diverse cohort, we hypothesized that childhood atopic dermatitis would be associated with higher prenatal omega-6 (n-6) and lower omega-3 (n-3) PUFAs.
Methods:
We included mother-child dyads, births 2006 to 2011, enrolled in the University of Tennessee Health Sciences Center Conditions Affecting Neurocognitive Development in Early Childhood cohort. Primary exposures included second trimester plasma n-3 and n-6 PUFA status and the ratio of the two (n-6:n-3). We assessed child current atopic dermatitis symptoms in the previous 12 months at age approximately 4 to 6 years. We investigated the association between PUFA exposures and atopic dermatitis using multivariable logistic regression, adjusting for potential confounders. We assessed for effect modification by maternal prenatal smoking, atopic disease history, and child sex.
Results:
Among 1131 women, 67% were African American and 42% had an atopic disease history; 17% of children had atopic dermatitis. Higher prenatal n-6 PUFAs were associated with increased relative odds of child atopic dermatitis (adjusted odds ratio: 1.25; confidence interval: 1.01-1.54 per interquartile range difference), and interaction models demonstrated that this association was seen in dyads in which the women had a history of atopic disease. Neither prenatal n-3 PUFAs nor n-6:n-3 were associated with child atopic dermatitis.
Conclusion:
In this racially diverse cohort, higher second trimester n-6 PUFAs were associated with atopic dermatitis in children of women with atopy. PUFAs may represent a modifiable risk factor for atopic dermatitis, particularly in individuals with a familial predisposition.
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