Prenatal exposure to environmental bisphenols over time and their association with childhood asthma, allergic rhinitis and atopic dermatitis in the ECHO consortium
- PMID: 39615574
- PMCID: PMC12120670
- DOI: 10.1016/j.envpol.2024.125415
Prenatal exposure to environmental bisphenols over time and their association with childhood asthma, allergic rhinitis and atopic dermatitis in the ECHO consortium
Abstract
Concerns persist about the potential impact of prenatal exposure to bisphenols (BP) and their replacement analogues on childhood asthma and allergies. Previous studies on single and small cohorts had limited statistical power, few investigated analogues BPF and BPS, and even fewer examined atopic outcomes. Our objective was to assess whether prenatal exposures to individual environmental bisphenols (BPA, BPF, BPS) influence risk of childhood asthma, allergic rhinitis, and atopic dermatitis. Data from the U.S. Environmental Influences on Child Health Outcomes (ECHO) consortium were harmonized on measures of prenatal urinary BPA, BPF and BPS and asthma and allergic rhinitis (ages 5-9 years) and atopic dermatitis (up to age 3 years) from 1905 mother-child pairs that were collected between 1998 and 2017. Across the 2012 federal ban of BPA from certain infant products, median BPA levels decreased from 1.11 ng/ml to 0.86 ng/ml; median BPF levels decreased from 0.51 ng/ml to 0.39 ng/ml; and median BPS levels increased from 0.23 ng/ml to 0.31 ng/ml (dilution adjusted; p < 0.001 for all three median comparisons). Prenatal measures of BPA, BPF, and BPS were unrelated to the risk of childhood asthma, allergic rhinitis, or atopic dermatitis in the total population. Modest sex-dependent effects were observed: only among girls, second tertile levels of BPF was associated with a reduced odds of asthma (odds ratio (OR) 0.27, 95% confidence interval (CI) 0.08, 0.93); a continuous index of prenatal BPS was associated with reduced odds of atopic dermatitis (OR 0.64, 95% CI 0.44, 0.93). The ongoing and changing patterns of exposure to bisphenols in the U.S. population require further study with additional attention to time windows of exposure and co-occurring social determinants of health, to continue to inform current policies and evaluate the importance of limiting exposure to BPA and its analogues on childhood asthma, allergic rhinitis, and atopic dermatitis.
Keywords: Bisphenols; Childhood allergy; Childhood asthma; Environmental influences on child health outcomes; Prenatal chemical exposure.
Copyright © 2024 Elsevier Ltd. All rights reserved.
Conflict of interest statement
Declaration of competing interest The authors declare the following financial interests/personal relationships which may be considered as potential competing interests:Scott Weiss reports financial support was provided by National Institutes of Health. Scott Weiss reports financial support was provided by UptoDate Inc. Rachel L. Miller reports financial support was provided by National Institutes of Health. Yuyan Wang reports financial support was provided by National Institutes of Health. Jenny Aalborg reports financial support was provided by National Institutes of Health. Akram N. Alshawabkeh reports financial support was provided by National Institutes of Health. Deborah H. Bennett reports financial support was provided by National Institutes of Health. Carrie V. Breton reports financial support was provided by National Institutes of Health. Jessie P. Buckley reports financial support was provided by National Institutes of Health. Dana Dabelea reports financial support was provided by National Institutes of Health. Anne L. Dunlop reports financial support was provided by National Institutes of Health. Assiamira Ferrara reports financial support was provided by National Institutes of Health. Griffith Gao reports financial support was provided by National Institutes of Health. Abigail Gaylord reports financial support was provided by National Institutes of Health. Diane R. Gold reports financial support was provided by National Institutes of Health. Tina Hartert reports financial support was provided by National Institutes of Health. Irva Hertz-Picciotto reports financial support was provided by National Institutes of Health. Lori A. Hoepner reports financial support was provided by National Institutes of Health. Margaret Karagas reports financial support was provided by National Institutes of Health. Catherine J. Karr reports financial support was provided by National Institutes of Health. Rachel S. Kelly reports financial support was provided by National Institutes of Health. Camilo Khatchikian reports financial support was provided by National Institute of Health. Mengling Liu reports financial support was provided by National Institutes of Health. John D. Meeker reports financial support was provided by National Institutes of Health. Thomas G. OConnor reports financial support was provided by National Institutes of Health. Alicia K. Peterson reports financial support was provided by National Institutes of Health. Sheela Sathyanarayana reports financial support was provided by National Institutes of Health. Joanne Sordillo reports financial support was provided by National Institutes of Health. Leonardo Trasande reports financial support was provided by National Institutes of Health. Yeyi Zhu reports financial support was provided by National Institutes of Health. Rachel L. Miller reports a relationship with UptoDate Inc that includes: consulting or advisory. Scott Weiss is on the Board of Histolix a digital pathology company. If there are other authors, they declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.
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