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Published on: March 6, 2018
Prenatal exposure to bisphenol A and risk of allergic diseases in early life
Aifen Zhou1,2, Huailong Chang1, Wenqian Huo1
1Key Laboratory of Environment and Health, Ministry of Education &Ministry of Environmental Protection, and State Key Laboratory of Environmental Health, School of Public Health, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China.
Insights
Prenatal exposure to bisphenol A (BPA) is linked to a higher risk of allergic diseases in infants. This association was particularly noted in female infants born to younger mothers.
Area of Science:
- Environmental health
- Pediatric allergy
- Toxicology
Background:
- Prenatal bisphenol A (BPA) exposure impacts the immune system, potentially promoting allergies and asthma.
- Human studies on prenatal BPA exposure and infant allergies are limited.
Purpose of the Study:
- To investigate the association between prenatal BPA exposure and the risk of allergic diseases in infants.
- To explore potential sex-specific and age-related differences in this association.
Main Methods:
- Maternal urine samples (n=412) were collected at delivery in Wuhan, China, to measure BPA concentrations.
- Infant allergic diseases (eczema, wheeze) were assessed at 6 months via questionnaires.
- Logistic regression analysis was used to determine the association between BPA levels and allergic disease risk.
Main Results:
- Mothers of infants with allergies had significantly higher urinary BPA levels compared to controls.
- Higher creatinine-adjusted maternal urinary BPA concentrations were associated with increased infant allergy risk.
- This association was significant in female infants (OR=1.36) and infants of mothers younger than 25 (OR=1.90).
Conclusions:
- Prenatal BPA exposure may increase the risk of allergic diseases in early life.
- The risk appears more pronounced in female infants and those born to younger mothers.
Background:
Prenatal exposure to bisphenol A (BPA) affects immune system and promotes allergy and asthma in mice, but findings in human studies are limited. We investigated whether prenatal exposure to BPA is associated with increased risk of allergic diseases in infants.
Methods:
We measured BPA concentrations in maternal urine samples collected at delivery from 412 women in Wuhan, China. The occurrence of allergic diseases including eczema and wheeze were assessed at age 6 mo through questionnaires. We used logistic regression to evaluate the association between urinary BPA levels and the risk of allergic diseases.
Results:
Mothers of infants with allergic diseases had significantly higher urinary BPA levels than those of infants without allergic diseases (median: 2.35 vs. 4.55 µg/l, P = 0.03). Increased risk of infant allergic diseases was associated with creatinine-adjusted maternal urinary BPA concentrations. And this association was limited to females (odds ratio (OR) = 1.36; 95% confidence interval (CI): 1.10-1.79) rather than males. After stratification by maternal age, the association was only significant in infants of mothers who were younger than 25 y old (OR = 1.90; 95% CI: 1.09-3.29).
Conclusion:
Prenatal exposure to BPA may potentially increase the risk of allergic diseases at very early life in female infants.
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