Michael S Bloom, Sudhi Upadhyaya, Adaeze W Nzegwu, Jordan R Kuiper, Jessie P Buckley, Judy Aschner, Dana Barr, Emily S Barrett, Deborah H Bennett, Dana Dabelea, Anne L Dunlop, Alma Fuller, Margaret Karagas, Donghai Liang, John Meeker, Rachel Miller, Thomas G O'Connor, Megan E Romano, Sheela Sathyanarayana, Anne P Starling, Annemarie Stroustrup, Deborah J Watkins
{"title":"Racial and ethnic differences in prenatal exposure to environmental phenols and parabens in the ECHO Cohort.","authors":"Michael S Bloom, Sudhi Upadhyaya, Adaeze W Nzegwu, Jordan R Kuiper, Jessie P Buckley, Judy Aschner, Dana Barr, Emily S Barrett, Deborah H Bennett, Dana Dabelea, Anne L Dunlop, Alma Fuller, Margaret Karagas, Donghai Liang, John Meeker, Rachel Miller, Thomas G O'Connor, Megan E Romano, Sheela Sathyanarayana, Anne P Starling, Annemarie Stroustrup, Deborah J Watkins","doi":"10.1038/s41370-025-00750-w","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>Research suggests racial/ethnic disparities in prenatal exposure to endocrine disrupting environmental phenols (EPs) in limited populations. However, no studies have investigated racial/ethnic disparities in prenatal EP exposure across the U.S.</p><p><strong>Objectives: </strong>To estimate demographic differences in prenatal urinary EPs among participants in the Environmental influences on Child Health Outcomes (ECHO) Cohort.</p><p><strong>Methods: </strong>An analysis of 4006 pregnant ECHO participants was performed, with 7854 specimens collected from 1999-2020. Racial/ethnic identity was self-reported. Urinary levels of 2,4-dichlorophenol (2,4-DCP), 2,5-dichlorophenol (2,5-DCP), benzophenone-3 (BP-3), bisphenols A (BPA), F (BPF), and S (BPS), and methyl- (MePb), ethyl- (EtPb), propyl- (PrPb), and butyl- (BuPb) parabens were measured at one or more time points during pregnancy. Effect estimates were adjusted for age, pre-pregnancy body mass index, educational level, gestational age and season at urine collection, and ECHO cohort.</p><p><strong>Results: </strong>Participants were classified as Hispanic of any race (n = 1658), non-Hispanic White (n = 1478), non-Hispanic Black (n = 490), and non-Hispanic Other (n = 362), which included individuals of multiple races. Urinary 2,4-DCP and 2,5-DCP concentrations were 2- to 4-fold higher among Hispanic, non-Hispanic Black, and non-Hispanic Other participants relative to non-Hispanic White participants. MePb was ~2-fold higher among non-Hispanic Black (95% confidence interval (CI): 1.7-3.1) and non-Hispanic Other (95% CI: 1.5-2.8) participants. PrPb was similarly higher among non-Hispanic Black (95% CI: 1.7-3.7) and non-Hispanic Other (95% CI: 1.3-3.1) participants. EtPb was higher among non-Hispanic Black participants (3.1-fold; 95% CI 1.7-5.8). BP-3 was lower in Hispanic (0.7-fold; 95% CI: 0.5-0.9), non-Hispanic Black (0.4-fold; 95% CI: 0.3-0.5), and non-Hispanic Other (0.5-fold; 95% CI: 0.4-0.7) participants. Urinary BuPb, BPA, BPF, and BPS were similar across groups.</p><p><strong>Impact statement: </strong>This multisite, observational cohort study investigated whether there are racial and ethnic differences in prenatal exposure to endocrine disrupting environmental phenols and parabens. Among 4006 participants from multiple U.S. cohorts who provided urine specimens during pregnancy, those who self-reported a racial and ethnic identity other than non-Hispanic White had higher urinary concentrations of 2,4-dichlorophenol, 2,5-dichlorophenol, methyl paraben, ethyl paraben, and propyl paraben and lower urinary concentrations of benzophenone-3 than those reporting as non-Hispanic White. These data show differences in prenatal concentrations of endocrine disrupting environmental phenols and parabens by racial and ethnic identity.</p>","PeriodicalId":15684,"journal":{"name":"Journal of Exposure Science and Environmental Epidemiology","volume":" ","pages":""},"PeriodicalIF":4.1000,"publicationDate":"2025-02-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Exposure Science and Environmental Epidemiology","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1038/s41370-025-00750-w","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"ENVIRONMENTAL SCIENCES","Score":null,"Total":0}
引用次数: 0
Abstract
Background: Research suggests racial/ethnic disparities in prenatal exposure to endocrine disrupting environmental phenols (EPs) in limited populations. However, no studies have investigated racial/ethnic disparities in prenatal EP exposure across the U.S.
Objectives: To estimate demographic differences in prenatal urinary EPs among participants in the Environmental influences on Child Health Outcomes (ECHO) Cohort.
Methods: An analysis of 4006 pregnant ECHO participants was performed, with 7854 specimens collected from 1999-2020. Racial/ethnic identity was self-reported. Urinary levels of 2,4-dichlorophenol (2,4-DCP), 2,5-dichlorophenol (2,5-DCP), benzophenone-3 (BP-3), bisphenols A (BPA), F (BPF), and S (BPS), and methyl- (MePb), ethyl- (EtPb), propyl- (PrPb), and butyl- (BuPb) parabens were measured at one or more time points during pregnancy. Effect estimates were adjusted for age, pre-pregnancy body mass index, educational level, gestational age and season at urine collection, and ECHO cohort.
Results: Participants were classified as Hispanic of any race (n = 1658), non-Hispanic White (n = 1478), non-Hispanic Black (n = 490), and non-Hispanic Other (n = 362), which included individuals of multiple races. Urinary 2,4-DCP and 2,5-DCP concentrations were 2- to 4-fold higher among Hispanic, non-Hispanic Black, and non-Hispanic Other participants relative to non-Hispanic White participants. MePb was ~2-fold higher among non-Hispanic Black (95% confidence interval (CI): 1.7-3.1) and non-Hispanic Other (95% CI: 1.5-2.8) participants. PrPb was similarly higher among non-Hispanic Black (95% CI: 1.7-3.7) and non-Hispanic Other (95% CI: 1.3-3.1) participants. EtPb was higher among non-Hispanic Black participants (3.1-fold; 95% CI 1.7-5.8). BP-3 was lower in Hispanic (0.7-fold; 95% CI: 0.5-0.9), non-Hispanic Black (0.4-fold; 95% CI: 0.3-0.5), and non-Hispanic Other (0.5-fold; 95% CI: 0.4-0.7) participants. Urinary BuPb, BPA, BPF, and BPS were similar across groups.
Impact statement: This multisite, observational cohort study investigated whether there are racial and ethnic differences in prenatal exposure to endocrine disrupting environmental phenols and parabens. Among 4006 participants from multiple U.S. cohorts who provided urine specimens during pregnancy, those who self-reported a racial and ethnic identity other than non-Hispanic White had higher urinary concentrations of 2,4-dichlorophenol, 2,5-dichlorophenol, methyl paraben, ethyl paraben, and propyl paraben and lower urinary concentrations of benzophenone-3 than those reporting as non-Hispanic White. These data show differences in prenatal concentrations of endocrine disrupting environmental phenols and parabens by racial and ethnic identity.
期刊介绍:
Journal of Exposure Science and Environmental Epidemiology (JESEE) aims to be the premier and authoritative source of information on advances in exposure science for professionals in a wide range of environmental and public health disciplines.
JESEE publishes original peer-reviewed research presenting significant advances in exposure science and exposure analysis, including development and application of the latest technologies for measuring exposures, and innovative computational approaches for translating novel data streams to characterize and predict exposures. The types of papers published in the research section of JESEE are original research articles, translation studies, and correspondence. Reported results should further understanding of the relationship between environmental exposure and human health, describe evaluated novel exposure science tools, or demonstrate potential of exposure science to enable decisions and actions that promote and protect human health.