TY - JOUR
T1 - Magnetic resonance and spectroscopic imaging in prenatal alcohol-exposed children
T2 - Preliminary findings in the caudate nucleus
AU - Cortese, Bernadette M.
AU - Moore, Gregory J.
AU - Bailey, Beth A.
AU - Jacobson, Sandra W.
AU - Delaney-Black, Virginia
AU - Hannigan, John H.
N1 - Funding Information:
The research that originally recruited many of the participants was supported in part by grants R01-AA09524 to SWJ, R01-DA08524 to VDB, and by the Fetal Alcohol Research Center at Wayne State University (P50-AA07606, R.J. Sokol, Director). The present research was supported in part by grant R01-DA016373 to VDB and by the Department of Obstetrics and Gynecology at Wayne State University. The authors thank S.K. O'Leary-Moore for helpful comments on the manuscript.
PY - 2006/9
Y1 - 2006/9
N2 - Magnetic resonance imaging (MRI) and magnetic resonance spectroscopic imaging (MRSI) offer unique, noninvasive methods of measuring, respectively, in vivo quantitative neuroanatomy and neurochemistry. The main purpose of the present study was to identify and compare the neuroanatomical and neurochemical abnormalities that are associated with prenatal exposure to alcohol in both fetal alcohol syndrome (FAS)-diagnosed children and those diagnosed with fetal alcohol effects (FAE). MR data of three age-, gender- and race-balanced groups of children, FAS-diagnosed, FAE-diagnosed and non-exposed controls, were compared. Effects of prenatal alcohol exposure, regardless of diagnosis, were found in the caudate nucleus. Specifically, a significantly smaller caudate nucleus was found for the FAS and FAE participants compared to the controls. In addition, the metabolite ratio of N-acetyl-aspartate to creatine (NAA/Cr), an indicator of neuronal function, in left caudate nucleus of both the FAS and FAE participants was elevated compared to the control group. Analysis of absolute concentrations revealed that the increase in the ratio of NAA/Cr was due to an increase in NAA alone. Although its exact function in the CNS is unknown, NAA is believed to be a neuronal marker due to its exclusive localization to neurons. Some also speculate a role for NAA in myelination. Elevated NAA in the prenatal alcohol-exposed participants could indicate a lack of normal program cell death, dendritic pruning and/or myelination during development. The present study demonstrates that prenatal alcohol-exposed children, with or without facial dysmorphology, have abnormal brain anatomy and chemistry.
AB - Magnetic resonance imaging (MRI) and magnetic resonance spectroscopic imaging (MRSI) offer unique, noninvasive methods of measuring, respectively, in vivo quantitative neuroanatomy and neurochemistry. The main purpose of the present study was to identify and compare the neuroanatomical and neurochemical abnormalities that are associated with prenatal exposure to alcohol in both fetal alcohol syndrome (FAS)-diagnosed children and those diagnosed with fetal alcohol effects (FAE). MR data of three age-, gender- and race-balanced groups of children, FAS-diagnosed, FAE-diagnosed and non-exposed controls, were compared. Effects of prenatal alcohol exposure, regardless of diagnosis, were found in the caudate nucleus. Specifically, a significantly smaller caudate nucleus was found for the FAS and FAE participants compared to the controls. In addition, the metabolite ratio of N-acetyl-aspartate to creatine (NAA/Cr), an indicator of neuronal function, in left caudate nucleus of both the FAS and FAE participants was elevated compared to the control group. Analysis of absolute concentrations revealed that the increase in the ratio of NAA/Cr was due to an increase in NAA alone. Although its exact function in the CNS is unknown, NAA is believed to be a neuronal marker due to its exclusive localization to neurons. Some also speculate a role for NAA in myelination. Elevated NAA in the prenatal alcohol-exposed participants could indicate a lack of normal program cell death, dendritic pruning and/or myelination during development. The present study demonstrates that prenatal alcohol-exposed children, with or without facial dysmorphology, have abnormal brain anatomy and chemistry.
KW - Caudate nucleus
KW - Fetal alcohol syndrome
KW - Magnetic resonance imaging spectroscopy
UR - http://www.scopus.com/inward/record.url?scp=33750704639&partnerID=8YFLogxK
U2 - 10.1016/j.ntt.2006.08.002
DO - 10.1016/j.ntt.2006.08.002
M3 - Article
C2 - 16996247
AN - SCOPUS:33750704639
SN - 0892-0362
VL - 28
SP - 597
EP - 606
JO - Neurotoxicology and Teratology
JF - Neurotoxicology and Teratology
IS - 5
ER -