Phosphatidylethanol Levels in Postpartum Women and Their Newborns in Uruguay and Brazil

Aileen E Baldwin1, Nicole Hayes2, Erika Ostrander3

  • 1United States Drug Testing Laboratories, Inc., (AEB), Des Plaines, Illinois.

Insights

Newborn screening for phosphatidylethanol (PEth) may help identify infants affected by prenatal alcohol exposure. PEth levels were significantly higher in newborns than in their mothers, suggesting its potential for early detection of fetal alcohol spectrum disorder (FASD).

Area of Science:

  • Neonatal screening
  • Biomarkers of prenatal substance exposure
  • Public health interventions for FASD

Background:

  • Growing interest in early identification of fetal alcohol spectrum disorder (FASD) for timely intervention.
  • Phosphatidylethanol (PEth) is a promising biomarker for universal newborn screening.
  • Prenatal alcohol exposure poses significant risks to infant development.

Purpose of the Study:

  • To compare phosphatidylethanol (PEth) levels in postpartum women and their newborns.
  • To evaluate PEth as a potential universal newborn screening tool for prenatal alcohol exposure.
  • To assess PEth levels in Uruguay and Brazil.

Main Methods:

  • Study involved 1,140 postpartum women and their newborns in Uruguay and Brazil.
  • Collected self-reported alcohol use during pregnancy data.
  • Analyzed maternal and newborn dried blood spot samples for PEth levels.

Main Results:

  • Newborns exhibited significantly higher PEth levels than their mothers in both study sites.
  • In Uruguay, 86.8% of newborns and 45.8% of mothers had PEth ≥ 8 ng/ml.
  • In Brazil, 76.9% of newborns and 33.2% of mothers had PEth ≥ 8 ng/ml.
  • Discrepancy noted between self-reported alcohol use and positive maternal PEth levels.

Conclusions:

  • Newborn PEth screening could be valuable in high-risk populations with prevalent prenatal alcohol use.
  • The underlying mechanism for higher newborn PEth levels compared to maternal levels requires further investigation.
  • PEth shows potential as a biomarker for identifying infants affected by prenatal alcohol exposure.
Abstract