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i n d e n t f y i
n g a l c o h o l - e x p o s e d p
r e g e n a c i e s t h r o u g h b
i o m a r k e r s
Moderate-to-heavy
alcohol use by pregnant women is known to be harmful to the
developing fetus. Currently, there is no specific laboratory
marker to indicate fetal alcohol syndrome. Obtaining such
a marker could lead to the identification and treatment of
women at risk for an alcohol-exposed pregnancy, who may not
otherwise provide this information because of the stigma associated
with prenatal alcohol use. Also, research has shown that early
identification of children with fetal alcohol exposure reduces
secondary disabilities resulting from the condition. Possible
biomarkers include maternal blood and meconium (first stool
of the newborn infant) testing. The studies described below
are designed to devise and test sensitive and specific biomarkers
to help identify alcohol-exposed pregnancies and/or newborns
exposed to alcohol prenatally.
FUNDED PROJECTS
University Hospital of Cleveland—Cleveland,
Ohio
It is estimated that 1% of all newborns are affected by prenatal
alcohol exposure. However, identifying alcohol-exposed newborns
is difficult. Currently, there is no systematic approach,
nor definitive laboratory tool that can be used for such identification.
A biological marker, fatty acid ethyl esters (FAEE), would
allow earlier identification and intervention for affected
infants, and recognition of women at risk for alcohol abuse.
This also facilitates research on dose-response relationships
between alcohol exposure and alcohol-related birth defects.
The project proposes that FAEE in meconium is a useful biological
marker for exposure of low-to-moderate maternal alcohol use
during pregnancy, and for identification of a group of infants
at high risk for poor neurodevelopmental outcomes. The study
seeks to validate FAEE in meconium as a biomarker of prenatal
exposure to alcohol.
University
of Maryland—Baltimore,
Maryland
The purpose of this study is to investigate the use of biochemical
tests and ultrasound findings to identify women who abuse
alcohol and are at risk for having a child affected adversely
by prenatal alcohol exposure. Criteria, derived from alcohol-use
questionnaires, biochemical markers and ultrasound studies,
are being developed to identify at-risk, pregnant women who
need special counseling or intervention. This information
will be correlated with infant development indices taken at
birth and at 6 and 12 months of age to predict the prenatal
risk for fetal alcohol syndrome (FAS) and other prenatal alcohol-related
conditions. Eliminating or reducing alcohol consumption during
pregnancy would have a significant effect on the incidence
of fetal alcohol syndrome and other prenatal alcohol-related
conditions.
Massachusetts General Hospital—Boston,
Massachusetts
The goals of this project are to: (1) identify women at risk
for having an alcohol-exposed pregnancy through a combination
of questionnaire screening and biochemical markers of alcohol
use, and (2) motivate the women at risk to decrease their
alcohol intake through brief intervention meetings and results
of their blood marker levels throughout their pregnancies.
Previous studies show that certain blood markers can be used
to identify alcohol-using pregnant women more accurately than
women’s self-reported use. This study will use a combination
of blood markers and self-report to identify women at risk
of having an alcohol-exposed pregnancy. Pregnant women receiving
prenatal care at obstetric clinics at several sites in the
Boston area receive a questionnaire to determine if they are
risk drinkers. The women who are not identified as risk drinkers
on the questionnaire serve as the comparison group for the
study. Women who are identified as risk drinkers are asked
to provide a blood sample, and a series of blood markers of
alcohol use are assessed. Women with positive blood markers
are then asked to participate in a series of brief interventions
and agree to ongoing monitoring of and feedback on the blood
markers throughout their pregnancy. Infant outcomes will be
assessed on all women participating in the study and the role
of specific markers on the achievement of alcohol abstinence
or reduction will also be explored.
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