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. 2023 Nov;131(11):117006.
doi: 10.1289/EHP11377. Epub 2023 Nov 14.

Prenatal Exposure to PFAS, Associations with Preterm Birth and Modification by Maternal Estrogen Levels: The Maoming Birth Study

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Prenatal Exposure to PFAS, Associations with Preterm Birth and Modification by Maternal Estrogen Levels: The Maoming Birth Study

Xiao-Di Qin et al. Environ Health Perspect. 2023 Nov.

Abstract

Background: Estrogens play a critical role in parturition, and poly- and perfluoroalkyl substances (PFAS), which have estrogenic effects, have been associated with preterm birth. However, the impact of estrogens on the association between PFAS and preterm birth is unknown.

Objective: The objective of this study is to investigate if estrogens modified the association between PFAS and preterm birth, using a nested case-control study design.

Methods: A total of 371 preterm births and 508 controls were selected from a birth cohort study in China between 2016 and 2018. Perfluorobutanoic acid (PFBA), perfluorohexanesulfonic acid (PFHxS) and its branched isomer, perfluorooctanoic acid (PFOA), perfluorooctanesulfonic acid (PFOS) and its branched isomer, and perfluorononanoic acid (PFNA) were quantified in maternal serum (mean gestational age of 32 wk). Estradiol and estriol were quantified in cord serum. Preterm birth was defined as live delivery at <37 gestational weeks. Causal mediation analysis was used to estimate the mediation and interaction effects of estrogen on the association between PFAS and preterm birth. Latent profile analysis was used to identify important estrogen profiles. Multiple linear regression was used to estimate associations between PFAS and preterm birth and interactions between PFAS and estrogens on preterm birth.

Results: Overall, higher odds ratios (ORs) of preterm birth were associated with each 1 ln-unit PFAS increase: PFBA [1.20, 95% confidence interval (CI): 1.14, 1.26], PFNA (1.30, 95% CI: 1.21, 1.39), PFOA (1.98, 95% CI: 1.54, 2.55), and PFOS (1.91, 95% CI: 1.76, 2.07) and its branched isomer (1.91, 95% CI: 1.90, 1.92). We detected statistically significant interactions between cord estradiol and PFAS on preterm birth, while no mediation effects of cord estrogen were observed. The ORs of PFOS (4.29, 95% CI: 1.31, 8.25), its branched isomer (6.71, 95% CI: 1.06, 11.91), and preterm birth were greater for participants with high cord estrogen levels than for participants with low cord estrogen levels.

Discussion: Our findings suggest that estrogen modified the association between maternal PFAS exposure and preterm birth. Further studies on maternal PFAS exposure and preterm birth, taking interaction effects of cord estrogens into account, are warranted. https://doi.org/10.1289/EHP11377.

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Figures

Figures 1 (a) and (b) are error bar graphs, plotting odds ratio for preterm birth, ranging from 0 to 10 in increments of 2 and odds ratio for preterm birth, ranging from 0 to 15 in increments of 5 (y-axis) across 736 cases of least estrogen; 120 cases of high estriol, perfluorooctanesulfonic acid; and 23 cases high estradiol; and 736 cases of least estrogen; 120 cases of high estriol, branched-perfluorooctanesulfonic acid; and 23 cases high estradiol (x-axis) for uppercase italic p for interaction.
Figure 1.
Logistic regression models for associations between preterm birth and serum PFOS (A) and br-PFOS (B) stratified by cord serum estrogen profile using latent profile analysis; least estrogen (n=736), high estriol (n=120), and high estradiol (n=23). All models were adjusted for age, maternal BMI, maternal education, infant sex, parity, environmental tobacco smoke, alcohol intake, household income, date of delivery, and biospecimen collection time during pregnancy. Additional details about the association from the analysis are in Table S12. Blue boxes indicate odds ratios; black bars indicate 95% confidence intervals. P for interaction test of estrogen profile by PFAS cross-product term. Note: BMI, body mass index; br, branch-; PFOS, perfluorooctanesulfonic acid.

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