Ethanol-induced face-brain dysmorphology patterns are correlative and exposure-stage dependent

Prenatal ethanol exposure is the leading preventable cause of congenital mental disability. Whereas a diagnosis of fetal alcohol syndrome (FAS) requires identification of a specific pattern of craniofacial dysmorphology, most individuals with behavioral and neurological sequelae of heavy prenatal et...

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Veröffentlicht in:PloS one 2012-08, Vol.7 (8), p.e43067
Hauptverfasser: Lipinski, Robert J, Hammond, Peter, O'Leary-Moore, Shonagh K, Ament, Jacob J, Pecevich, Stephen J, Jiang, Yi, Budin, Francois, Parnell, Scott E, Suttie, Michael, Godin, Elizabeth A, Everson, Joshua L, Dehart, Deborah B, Oguz, Ipek, Holloway, Hunter T, Styner, Martin A, Johnson, G Allan, Sulik, Kathleen K
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container_issue 8
container_start_page e43067
container_title PloS one
container_volume 7
creator Lipinski, Robert J
Hammond, Peter
O'Leary-Moore, Shonagh K
Ament, Jacob J
Pecevich, Stephen J
Jiang, Yi
Budin, Francois
Parnell, Scott E
Suttie, Michael
Godin, Elizabeth A
Everson, Joshua L
Dehart, Deborah B
Oguz, Ipek
Holloway, Hunter T
Styner, Martin A
Johnson, G Allan
Sulik, Kathleen K
description Prenatal ethanol exposure is the leading preventable cause of congenital mental disability. Whereas a diagnosis of fetal alcohol syndrome (FAS) requires identification of a specific pattern of craniofacial dysmorphology, most individuals with behavioral and neurological sequelae of heavy prenatal ethanol exposure do not exhibit these defining facial characteristics. Here, a novel integration of MRI and dense surface modeling-based shape analysis was applied to characterize concurrent face-brain phenotypes in C57Bl/6J fetuses exposed to ethanol on gestational day (GD)7 or GD8.5. The facial phenotype resulting from ethanol exposure depended upon stage of insult and was predictive of unique patterns of corresponding brain abnormalities. Ethanol exposure on GD7 produced a constellation of dysmorphic facial features characteristic of human FAS, including severe midfacial hypoplasia, shortening of the palpebral fissures, an elongated upper lip, and deficient philtrum. In contrast, ethanol exposure on GD8.5 caused mild midfacial hypoplasia and palpebral fissure shortening, a shortened upper lip, and a preserved philtrum. These distinct, stage-specific facial phenotypes were associated with unique volumetric and shape abnormalities of the septal region, pituitary, and olfactory bulbs. By demonstrating that early prenatal ethanol exposure can cause more than one temporally-specific pattern of defects, these findings illustrate the need for an expansion of current diagnostic criteria to better capture the full range of facial and brain dysmorphology in fetal alcohol spectrum disorders.
doi_str_mv 10.1371/journal.pone.0043067
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subjects Abnormalities
Alcohols
Analysis
Animals
Biology
Brain
Brain - abnormalities
Brain - embryology
Brain research
Care and treatment
Chemical properties
Childrens health
Developmental biology
Diagnosis
Diagnostic systems
Dysmorphology
Elongation
Ethanol
Ethanol - adverse effects
Exposure
Face - abnormalities
Face - embryology
Female
Fetal Alcohol Spectrum Disorders - etiology
Fetal Alcohol Spectrum Disorders - pathology
Fetal alcohol syndrome
Fetuses
Genetic aspects
Health aspects
Humans
Hypoplasia
Lip
Magnetic Resonance Imaging
Medicine
Mice
Microscopy
Neurological complications
NMR
Nuclear magnetic resonance
Olfactory bulb
Phenotypes
Pituitary
Pregnancy
Pregnant women
Prenatal experience
Psychiatry
Schizophrenia
Studies
Volumetric analysis
title Ethanol-induced face-brain dysmorphology patterns are correlative and exposure-stage dependent
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