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A Comprehensive Assessment of Associations between Prenatal Phthalate Exposure and the Placental Transcriptomic Landscape. | LitMetric

AI Article Synopsis

  • Phthalates, which are common endocrine-disrupting chemicals, can affect placental function and fetal development when pregnant women are exposed during the second and third trimesters.
  • The study analyzed urine samples from 760 pregnant women to link specific phthalate metabolites to changes in placental gene and lncRNA expression at birth, revealing significant associations with multiple genes and biological pathways.
  • Findings showed that certain phthalates, particularly in the second and third trimesters, correlated with altered expression of 18 genes and 27 biological pathways in the placenta, suggesting potential mechanisms for adverse health outcomes in children.

Article Abstract

Background: Phthalates are commonly used endocrine-disrupting chemicals that are ubiquitous in the general population. Prenatal phthalate exposure may alter placental physiology and fetal development, leading to adverse perinatal and childhood health outcomes.

Objective: We examined associations between prenatal phthalate exposure in the second and third trimesters and the placental transcriptome at birth, including genes and long noncoding RNAs (lncRNAs), to gain insight into potential mechanisms of action during fetal development.

Methods: The ECHO PATHWAYs consortium quantified 21 urinary phthalate metabolites from 760 women enrolled in the CANDLE study (Shelby County, TN) using high-performance liquid chromatography-tandem mass spectrometry. Placental transcriptomic data were obtained using paired-end RNA sequencing. Linear models were fitted to estimate separate associations between maternal urinary phthalate metabolite concentration during the second and third trimester and placental gene expression at birth, adjusted for confounding variables. Genes were considered differentially expressed at a Benjamini-Hochberg false discovery rate (FDR) . Associations between phthalate metabolites and biological pathways were identified using self-contained gene set testing and considered significantly altered with an FDR-adjusted .

Results: We observed significant associations between second-trimester phthalate metabolites mono (carboxyisooctyl) phthalate (MCIOP), mono-2-ethyl-5-carboxypentyl phthalate, and mono-2-ethyl-5-oxohexyl phthalate and 18 genes in total, including four lncRNAs. Specifically, placental expression of was associated with multiple phthalate metabolites. Third-trimester MCIOP and mono-isobutyl phthalate concentrations were significantly associated with placental expression of 18 genes and two genes, respectively. Expression of genes within 27 biological pathways was associated with mono-methyl phthalate, MCIOP, and monoethyl phthalate concentrations.

Discussion: To our knowledge, this is the first genome-wide assessment of the relationship between the placental transcriptome at birth and prenatal phthalate exposure in a large and diverse birth cohort. We identified numerous genes and lncRNAs associated with prenatal phthalate exposure. These associations mirror findings from other epidemiological and analyses and may provide insight into biological pathways affected by phthalate exposure. https://doi.org/10.1289/EHP8973.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8415559PMC
http://dx.doi.org/10.1289/EHP8973DOI Listing

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