Limits of usual biochemical alcohol markers in cord blood at term: a fetal/maternal population-based study

Clin Chem Lab Med. 2007;45(4):546-8. doi: 10.1515/CCLM.2007.098.

Abstract

Background: After maternal alcohol consumption during pregnancy, many neonates affected by less apparent forms of fetal alcohol syndrome disorder (FASD) do not receive proper diagnosis or treatment. There is thus a need for laboratory markers for early detection of alcohol-exposed neonates. The aim of our study was to assess the efficiency of the usual alcohol biomarkers measured in cord blood to identify alcohol-exposed neonates immediately after birth.

Methods: A 1-year study was conducted in the labor wards of the maternity units of the Auvergne, Central France at the time of term delivery. The patients answered an anonymous self-completion survey concerning alcohol use (Alcohol Use Disorder Identification Test; AUDIT) during their pregnancy. Aspartate aminotransferase, alanine aminotransferase, and gamma-glutamyltransferase concentrations and the percentage of carbohydrate-deficient transferrin were measured in maternal and cord blood.

Results: We collected 870 maternal-fetal sample pairs. Two cases (0.2%) of typical FASD were detected. We report a non-significant correlation between maternal and cord blood biomarkers. None of the cord blood biomarkers differed significantly between newborns of alcohol-exposed and unexposed mothers.

Conclusions: We demonstrate that the usual alcohol biomarkers are not effective in cord blood for identifying alcohol-exposed neonates.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Biomarkers / blood*
  • Ethanol / blood*
  • Female
  • Fetal Blood / chemistry*
  • Humans
  • Infant, Newborn
  • Neonatal Screening*
  • Pregnancy
  • Prospective Studies

Substances

  • Biomarkers
  • Ethanol