Development of an Epigenetic Biomarker for Prediction of Fetal Alcohol Spectrum Disorder



Status:Recruiting
Conditions:Women's Studies
Therapuetic Areas:Reproductive
Healthy:No
Age Range:Any
Updated:4/22/2018
Start Date:April 12, 2018
End Date:April 2020
Contact:Stefan Maxwell, MD
Email:neodoc1124@gmail.com
Phone:304-388-2238

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The objective of the study is to validate epigenetic changes as biomarkers in a prospective
sampling of newborn blood samples collected at birth (umbilical cord blood) and during
routine screening (heel stick blood) in newborns concurrently tested for alcohol exposure
levels by PEth blood spot testing.

Fetal alcohol spectrum disorders (FASD) are a group of conditions that can occur in a person
whose birth mother consumed alcohol during pregnancy. The effects can include physical
problems and/or difficulties with behavior and learning. When clinicians identify FASD early,
intervention approaches can minimize the potential impact and lessen or even prevent
disabilities. Thus, objective markers for prenatal alcohol exposure are desired.

Using dried blood spots from the umbilical cord and a heel stick of newborns, this study will
use Phosphatidylethanol (PEth), a novel biomarker for alcohol exposure, to identify and
characterize infants' exposure to alcohol before birth. Additionally, the dried blood spots
will used to validate the use of screening assays using epigenetic changes as markers for
prenatal alcohol exposure. Epigenetic changes are heritable changes in DNA that affect DNA
function but do not change DNA sequence. The use of PEth testing will allow for the
correlation of prenatal alcohol exposure levels with epigenetic changes. Women will be
consented prior to delivery for participation in this prospective study. The study will be
conducted in collaboration with United States Drug Testing Laboratories, Inc. (USDTL).

Women:

Inclusion criteria

- Women aged ≥ 18 years and currently pregnant at time of enrollment

- Women who plan to and then deliver their infants at CAMC Women and Children's Hospital

Exclusion criteria

- Women aged < 18 years

- Women not pregnant

- Women who do not plan to deliver or did not end up delivering their infants at CAMC
Women and Children's Hospital

Infants:

Inclusion criteria

- Birth mother was consented prior to delivery

- Live birth at CAMC Women and Children's Hospital

Exclusion criteria

- Birth mother was NOT consented prior to delivery

- Stillborn
We found this trial at
1
site
Charleston, West Virginia 25304
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Charleston, WV
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