Fatty Acid Ethyl Esters in Meconium: Are They Biomarkers of Fetal Alcohol Exposure and Effect?

• Published in: Alcoholism, clinical and experimental research Vol. 30; no. 7; pp. 1152 - 1159
• Main Authors: Ostrea Jr, Enrique M., Hernandez, Joel D., Bielawski, Dawn M., Kan, Jack M., Leonardo, Gregorio M., Abela, Michelle Buda, Church, Michael W., Hannigan, John H., Janisse, James J., Ager, Joel W., Sokol, Robert J.
• Format: Journal Article
• Language: English
• Published: Malden, USA Blackwell Publishing Inc 01.07.2006; Lippincott Williams & Wilkins
• Subjects: Adult; Alcohol Drinking - metabolism; Alcoholism and acute alcohol poisoning; Arachidonic Acids - metabolism; Biological and medical sciences; Biomarkers - metabolism; Esters - metabolism; Ethanol - pharmacology; Ethyl Arachidonate; Ethyl Docosahexanoate; Ethyl Laurate; Ethyl Linoleate; Ethyl Linolenate; Ethyl Myristate; Ethyl Oleate; Ethyl Palmitate; Fatty Acid Ethyl Esters; Fatty Acids - metabolism; Female; Fetal Alcohol Syndrome; Fetus - drug effects; Gas Chromatography/Mass Spectroscopy; Humans; Infant, Newborn; Maternal Alcoholism; Meconium - metabolism; Medical sciences; Pregnancy; Toxicology; Fetal alcohol syndrome; Ethyl Linolenate; Maternal Alcoholism; Biological marker; Lipids; Alcoholic beverage; Ester; Gas Chromatography/Mass Spectroscopy; Mother; Fetus; Ethyl Docosahexanoate; Ethanol; Ethyl Linoleate; Fatty Acid Ethyl Esters; Ethyl Myristate; Alcoholism; Exposure; Fatty acids; Gas chromatography; Newborn diseases; Ethyl Palmitate; Ethyl Laurate; Meconium; Ethyl Oleate; Ethyl Arachidonate; Mass spectrometry
• ISSN: 0145-6008; 1530-0277
• DOI: 10.1111/j.1530-0277.2006.00131.x

Background: Biomarkers of fetal exposure to alcohol are important to establish so that early detection and intervention can be made on these infants to prevent undesirable outcomes. The aim of this study was to analyze long‐chain fatty acid ethyl esters (FAEEs) in meconium as potential biomarkers of fetal alcohol exposure and effect. Methods: Fatty acid ethyl esters were analyzed in the meconium of 124 singleton infants by positive chemical ionization gas chromatography/mass spectrometry (GC/MS) and correlated to maternal ethanol use. Results: A total of 124 mother/infant dyads were enrolled in the study: 31 were in the control group and 93 were in the alcohol‐exposed group. The incidence (28% vs 9.7%, p=0.037) of ethyl linoleate detected in meconium was significantly higher in the alcohol‐exposed groups than the control groups. Similarly, when the concentrations of ethyl linoleate in meconium were grouped (trichotomized), there was a significant linear by linear association between alcohol exposure and group concentrations of ethyl linoleate (p=0.013). Furthermore, only alcohol‐exposed infants were found in the group with the highest ethyl linoleate concentration. The sensitivity of ethyl linoleate in detecting prenatal alcohol exposure was only 26.9%, and its specificity and positive predictive value were 96.8 and 96.2%, respectively. There was no significant correlation between the concentration of ethyl linoleate in meconium and absolute alcohol consumed (oz) per drinking day across pregnancy, although a trend toward a positive correlation is seen at lower amounts of alcohol consumed. Among the polyunsaturated, long‐chain FAEEs, there was weak evidence that the incidence (21.5% vs 6.5%, p=0.057) and concentration (p=0.064) of ethyl arachidonate (AA) were significantly higher in the alcohol‐exposed groups than the control groups. Ethyl linolenate and ethyl docosahexanoate (DHA) in meconium were found only in the alcohol group, although not at statistically significant levels. Highly significant correlations were found among the concentrations of ethyl linoleate, ethyl linolenate, ethyl AA, and ethyl DHA in meconium (correlations ranged between rs=0.203, p=0.024; and rs=0.594, p<0.001). Conclusion: We conclude that FAEEs in meconium, particularly ethyl linoleate and ethyl AA, are biomarkers of high specificity for prenatal exposure to alcohol in newborn infants. We also propose that ethyl AA and DHA could be potential biomarkers of fetal alcohol effects on the developing fetal brain and should be investigated further.