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. 2022 Jul 28;188(2):153-179.
doi: 10.1093/toxsci/kfac060.

Phthalate Exposures and Placental Health in Animal Models and Humans: A Systematic Review

Affiliations

Phthalate Exposures and Placental Health in Animal Models and Humans: A Systematic Review

Talia N Seymore et al. Toxicol Sci. .

Abstract

Phthalates are ubiquitous compounds known to leach from the plastic products that contain them. Due to their endocrine-disrupting properties, a wide range of studies have elucidated their effects on reproduction, metabolism, neurodevelopment, and growth. Additionally, their impacts during pregnancy and on the developing fetus have been extensively studied. Most recently, there has been interest in the impacts of phthalates on the placenta, a transient major endocrine organ critical to maintenance of the uterine environment and fetal development. Phthalate-induced changes in placental structure and function may have significant impacts on the course of pregnancy and ultimately, child health. Prior reviews have described the literature on phthalates and placental health; however to date, there has been no comprehensive, systematic review on this topic. Here, we review 35 papers (24 human and 11 animal studies) and summarize phthalate exposures in relation to an extensive set of placental measures. Phthalate-related alterations were reported for placental morphology, hormone production, vascularization, histopathology, and gene/protein expression. The most consistent changes were observed in vascular and morphologic endpoints, including cell composition. These changes have implications for pregnancy complications such as preterm birth and intrauterine growth restriction as well as potential ramifications for children's health. This comprehensive review of the literature, including common sources of bias, will inform the future work in this rapidly expanding field.

Keywords: endocrine disruptors; phthalates; placenta; pregnancy.

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Figures

Graphical Abstract
Graphical Abstract
Figure 1.
Figure 1.
PRISMA flow diagram.

References

    1. Adibi J. J., Buckley J. P., Lee M. K., Williams P. L., Just A. C., Zhao Y., Bhat H. K., Whyatt R. M. (2017). Maternal urinary phthalates and sex-specific placental mRNA levels in an urban birth cohort. Environ. Health 16, 35. - PMC - PubMed
    1. Adibi J. J., Layden A. J., Birru R. L., Miragaia A., Xun X., Smith M. C., Yin Q., Millenson M. E., O'Connor T. G., Barrett E. S., et al. (2021). First trimester mechanisms of gestational sac placental and foetal teratogenicity: A framework for birth cohort studies. Hum. Reprod. Update 27, 747–770. - PMC - PubMed
    1. Adibi J. J., Lee M. K., Naimi A. I., Barrett E., Nguyen R. H., Sathyanarayana S., Zhao Y., Thiet M. P., Redmon J. B., Swan S. H. (2015). Human chorionic gonadotropin partially mediates phthalate association with male and female anogenital distance. J. Clin. Endocrinol. Metab. 100, E1216–E1224. - PMC - PubMed
    1. Adibi J. J., Whyatt R. M., Hauser R., Bhat H. K., Davis B. J., Calafat A. M., Hoepner L. A., Perera F. P., Tang D., Williams P. L. (2010). Transcriptional biomarkers of steroidogenesis and trophoblast differentiation in the placenta in relation to prenatal phthalate exposure. Environ. Health Perspect. 118, 291–296. - PMC - PubMed
    1. Ádori C., Glück L., Barde S., Yoshitake T., Kovacs G. G., Mulder J., Maglóczky Z., Havas L., Bölcskei K., Mitsios N., et al. (2015). Critical role of somatostatin receptor 2 in the vulnerability of the central noradrenergic system: New aspects on Alzheimer’s disease. Acta Neuropathol. 129, 541–563. - PubMed

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