4.7 Article

Prenatal Exposure to Bisphenols and Phthalates and Postpartum Depression: The Role of Neurosteroid Hormone Disruption

Journal

JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM
Volume 106, Issue 7, Pages 1887-1899

Publisher

ENDOCRINE SOC
DOI: 10.1210/clinem/dgab199

Keywords

Postpartum depression; phthalate; bisphenol; progesterone; allopregnanolone

Funding

  1. NYU Center for the Investigation of Environmental Hazards pilot project program
  2. National Institutes of Health Office of the Director grant [UG3/UH3OD023305]
  3. National Institutes of Environmental Health Sciences [P30ES000260]

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The study investigated the associations between urinary bisphenols and phthalates in early and midpregnancy with serum hormone concentrations and postpartum depression symptoms. The results suggested that certain phthalates were related to lower progesterone levels and increased odds of PPD, indicating a potential influence of endocrine disrupting chemicals on hormonal shifts during pregnancy and PPD.
Context: Postpartum depression (PPD) is a serious psychiatric disorder. While causes remain poorly understood, perinatal sex hormone fluctuations are an important factor, and allopregnanolone in particular has emerged as a key determinant. Although synthetic environmental chemicals such as bisphenols and phthalates are known to affect sex hormones, no studies have measured allopregnanolone and the consequences of these hormonal changes on PPD have not been interrogated. Objective: To investigate associations of repeated measures of urinary bisphenols and phthalates in early and midpregnancy with serum pregnenolone, progesterone, allopregnanolone, and pregnanolone concentrations in midpregnancy and PPD symptoms at 4 months postpartum. Methods: Prospective cohort study of 139 pregnant women recruited between 2016 and 2018. Bisphenols and phthalates were measured in early and midpregnancy urine samples. Serum sex steroid hormone concentrations were measured in midpregnancy. PPD was assessed at 4 months postpartum using the Edinburgh Postnatal Depression Scale (EPDS). Multiple informant models were fit using generalized estimating equations. Serum levels of allopregnanolone, progesterone, pregnanolone, and pregnenolone were examined as log-transformed continuous variables. PPD symptoms were examined as continuous EPDS scores and dichotomously with scores >= 10 defined as PPD. Results: Di-n-octyl phthalate (DnOP) and diisononyl phthalate (DiNP) metabolites were associated with reduced progesterone concentrations. Log-unit increases in Sigma DnOP and Sigma DiNP predicted 8.1% (95% CI -15.2%, -0.4%) and 7.7% (95% CI -13.3%, -1.7%) lower progesterone, respectively. Sigma DnOP was associated with increased odds of PPD (odds ratio 1.48; 95% CI 1.04, 2.11). Conclusion: Endocrine disrupting chemicals may influence hormonal shifts during pregnancy as well as contribute to PPD.

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