Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2025 Jan 1:958:178116.
doi: 10.1016/j.scitotenv.2024.178116. Epub 2024 Dec 17.

Prenatal exposure to phthalates and phthalate replacements in relation to chorionic plate surface vasculature at delivery

Emily S Barrett  1 , David Skrill  2 , Elaine Zhou  3 , Sally W Thurston  4 , Theresa Girardi  5 , Jessica Brunner  6 , Hai-Wei Liang  7 , Richard K Miller  8 , Carolyn M Salafia  9 , Thomas G O'Connor  10 , Jennifer J Adibi  7
Affiliations

Prenatal exposure to phthalates and phthalate replacements in relation to chorionic plate surface vasculature at delivery

Emily S Barrett et al. Sci Total Environ. .

Abstract

Pregnant people are ubiquitously exposed to endocrine-disrupting phthalates through consumer products and food. The placenta may be particularly vulnerable to the adverse effects of phthalates, with evidence from animal models suggesting impacts on placental development and vascularization. We translate this research to humans, examining gestational exposure to phthalates and phthalate replacements in relation to novel markers of chorionic plate surface vascularization. Phthalate and phthalate replacement metabolites were measured in first trimester urine from pregnant participants in the Understanding Pregnancy Signals and Infant Development (UPSIDE) cohort (n = 154). At delivery, placentae underwent specialized 2D and 3D digital imaging to quantify chorionic plate surface vasculature. Using weighted quantile g-computation mixtures methods as well as multivariable linear regression models examining individual metabolites, we evaluated associations with overall chorionic plate surface area and five chorionic plate surface vascular measures, adjusting for covariates. We additionally examined interactions with placental sex. Exposure to a phthalate mixture was associated with longer total arterial arc length (β = 9.64 cm; 95%CI: 1.68, 17.59), shorter mean arterial arc length (β = -0.07 cm; 95%CI: -0.14, -0.01), and more arterial branch points (β = 5.77; 95%CI: 1.56, 9.98), but not chorionic plate surface area. In models considering individual metabolites and their molar sums, results were strongest for the metabolites of Di-isobutyl phthalate (DiBP), Di-isononyl phthalate (DiNP), and Di(2-ethylhexyl) phthalate (DEHP). Associations with metabolites of phthalate replacements tended to be in the same direction but weaker. Few sex differences were observed. Gestational phthalate exposure may be associated with alterations in placental chorionic plate surface vasculature characterized by more branching and shorter segments. These alterations may have implications for placental perfusion and suggest a placental mechanism by which phthalates may impact fetal development.

Keywords: Chorionic plate vasculature; Phthalate replacements; Phthalates; Placenta; Pregnancy.

PubMed Disclaimer

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: Emily Barrett reports financial support was provided by Rutgers School of Public Health. 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.

References

    1. Adibi JJ, Layden AJ, Birru RL, Miragaia A, Xun X, Smith MC, et al. First trimester mechanisms of gestational sac placental and foetal teratogenicity: a framework for birth cohort studies. Hum Reprod Update 2021; 27: 747–770. - PMC - PubMed
    1. Ahbab MA, Güven C, Koçkaya EA, Barlas N. Comparative developmental toxicity evaluation of di- n-hexyl phthalate and dicyclohexyl phthalate in rats. Toxicol Ind Health 2017; 33: 696–716. - PubMed
    1. Barakat R, Seymore T, Lin PP, Park CJ, Ko CJ. Prenatal exposure to an environmentally relevant phthalate mixture disrupts testicular steroidogenesis in adult male mice. Environ Res 2019; 172: 194–201. - PMC - PubMed
    1. Barrett ES, Corsetti M, Day D, Thurston SW, Loftus CT, Karr CJ, et al. Prenatal phthalate exposure in relation to placental corticotropin releasing hormone (pCRH) in the CANDLE cohort. Environ Int 2022; 160: 107078. - PMC - PubMed
    1. Bedell SM, Lyden GR, Sathyanarayana S, Barrett ES, Ferguson KK, Santilli A, et al. First- and Third-Trimester Urinary Phthalate Metabolites in the Development of Hypertensive Diseases of Pregnancy. Int J Environ Res Public Health 2021; 18. - PMC - PubMed

LinkOut - more resources