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ABSTRACT: Background
Acetaminophen is a commonly used medication by pregnant women and is known to cross the placenta. However, little is known about the biological mechanisms that regulate acetaminophen in the developing offspring. Cytochrome 2E1 (CYP2E1) is the primary enzyme responsible for the conversion of acetaminophen to its toxic metabolite. Ex vivo studies have shown that the CYP2E1 gene expression in human fetal liver and placenta is largely controlled by DNA methylation (DNAm) at CpG sites located in the gene body of CYP2E1 at the 5' end. To date, no population studies have examined the association between acetaminophen metabolite and fetal DNAm of CYP2E1 at birth.Methods
We utilized data from the Boston Birth Cohort (BBC) which represents an urban, low-income, racially an
SUBMITTER: Li Y
PROVIDER: S-EPMC10439592 | biostudies-literature | 2023 Aug
REPOSITORIES: biostudies-literature