Jul 2026· Journal of the Endocrine Society· Vol 10· 0 citations· 58 references
Medicine
TL;DR
Certain urinary phthalate biomarkers, particularly MEP and ΣPCP, were associated with higher blood pressure levels in pregnancy, with implications for HDP.
Abstract
Abstract Introduction Some phthalates and their replacements are endocrine disrupting chemicals (EDCs) found in consumer products and linked to hypertensive disorders of pregnancy (HDP). Few studies have evaluated associations between EDCs and gestational blood pressure. Objective To evaluate associations between EDC biomarkers with gestational blood pressure. Methods The Environmental Reproductive and Glucose Outcomes study (N = 338) measured urinary concentrations of 18 phthalate and replacement metabolites and systolic (SBP) and diastolic (DBP) blood pressure at 3 pregnancy study visits (median: 12, 19, and 26 weeks’ gestation). Individual metabolite concentrations and summary measures based on common source or mechanism (eg, ΣPersonal care products [ΣPCP]) were log2-transformed, specific-gravity corrected, and modeled continuously and in quartiles. We estimated covariate-adjusted associations of individual metabolites and, summary measures with blood pressure using linear regression, and with HDP using log-binomial regression, assessing metabolite mixtures using Bayesian Kernel Machine Regression. Results HDP prevalence was 12.7%. Higher concentrations of monoethyl phthalate (MEP) and ΣPCP were most consistently associated with SBP and DBP elevations at visit 3. Higher concentrations of MEP (Q4 vs Q1) were associated with 4.59 mmHg higher SBP (95% CI: 0.04, 9.15), and higher ΣPCP (Q3 vs Q1) were associated with 5.78 mmHg (95% CI: 1.59, 9.97). Higher MEP and ΣPCP (Q4 vs Q1) were positively linked to DBP elevations of 4.51 to 4.70 mmHg. Other phthalate biomarkers were associated with blood pressure at specific time points. Discussion Certain urinary phthalate biomarkers, particularly MEP and ΣPCP, were associated with higher blood pressure levels in pregnancy, with implications for HDP.
Co-exposure to specific PAE and BP metabolites, particularly MnBP and BP-8, is positively associated with EPT in girls, highlighting that co-exposure to specific PAE and BP metabolites is positively associated with EPT in girls.
Zhi Li, Jing-Yi Tang, Yang Chen et al.· Ecotoxicology and Environmen...· 0 citations
A bi-directional relationship between phthalate exposure and estradiol levels in US males aged 20 years and older was observed and Demographic factors of race and ethnicity, marital status, country of origin, body mass index, and smoking status were correlated with abnormal estradiol levels.
Humairat H. Rahman, Weston R. Stokey, S. Munson-McGee· Reproductive Toxicology· 0 citations
BACKGROUND
Synthetic phenolic antioxidants (SPAs) are widely used industrial additives. This prospective cohort study aimed to explore the associations between maternal SPA exposure and blood pressure level throughout pregnancy.
METHODS
Based on a prospective birth cohort enrolling 1368 pregnant women from Ma'anshan,...
Hualong Zhen, Han-xin Gong, Lu Chen et al.· Environmental Research· 0 citations
Introduction Phthalates (PAEs) are endocrine-disrupting chemicals, yet the association between prenatal PAE exposure and maternal blood immune cells remains unclear. Here, we enrolled 2,581 pregnant women, including 287 in the first trimester (gestational weeks 1–12), 807 in the second trimester (gestational weeks 13–2...
Yi Zhang, Lin Tao· Frontiers in Public Health· 0 citations
DII and DTAC may be related to inflammatory biomarker variability in late pregnancy, and urinary and estimated dietary BPA exposure in conjunction with DII and DTAC showed consistent adjusted associations with maternal oxidative stress or inflammatory biomarkers or significant associations with fetal/neonatal outcomes.
Low-density lipoprotein cholesterol and neutrophil-to-lymphocyte ratio were co-primary outcomes; systemic immune–inflammation index (SII) was secondary; Adjusted models used multiple imputation and false-discovery-rate (FDR) correction.
C. Buonerba, P. Montuori, E. Esposito et al.· Toxics· 1 citation
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