Biobehavioral Markers of Adverse Effect in Fetal Alcohol Spectrum Disorders

被引:0
作者
Sandra W. Jacobson
Joseph L. Jacobson
Mark E. Stanton
Ernesta M. Meintjes
Christopher D. Molteno
机构
[1] Wayne State University School of Medicine,Department of Psychiatry and Behavioral Neurosciences
[2] University of Cape Town,Department of Human Biology, Faculty of Health Sciences
[3] University of Cape Town,Department of Psychiatry and Mental Health, Faculty of Health Sciences
[4] University of Delaware,Department of Psychology
[5] University of Cape Town,MRC/UCT Medical Imaging Research Unit
来源
Neuropsychology Review | 2011年 / 21卷
关键词
Fetal alcohol syndrome; Eyeblink conditioning; Arithmetic; Fetal alcohol spectrum disorders; Biomarkers; Behavioral phenotype; Prenatal alcohol exposure;
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摘要
Identification of children with fetal alcohol spectrum disorders (FASD) is difficult because information regarding prenatal exposure is often lacking, a large proportion of affected children do not exhibit facial anomalies, and no distinctive behavioral phenotype has been identified. Castellanos and Tannock have advocated going beyond descriptive symptom-based approaches to diagnosis to identify biomarkers derived from cognitive neuroscience. Classical eyeblink conditioning and magnitude comparison are particularly promising biobehavioral markers of FASD—eyeblink conditioning because a deficit in this elemental form of learning characterizes a very large proportion of alcohol-exposed children; magnitude comparison because it is a domain of higher order cognitive function that is among the most sensitive to fetal alcohol exposure. Because the neural circuitry mediating both these biobehavioral markers is well understood, they have considerable potential for advancing understanding of the pathophysiology of FASD, which can contribute to development of treatments targeted to the specific deficits that characterize this disorder.
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[1]  
Abel EL(1995)An update on the general incidence of FAS: FAS is not an equal opportunity deficit Neurotoxicology and Teratology 17 437-443
[2]  
Anderson CM(2002)Effects of methylphenidate on functional magnetic resonance relaxometry of the cerebellar vermis in boys with ADHD The American Journal of Psychiatry 159 1322-1328
[3]  
Polcari A(2001)Brain dysmorphology in individuals with severe prenatal alcohol exposure Developmental Medicine and Child Neurology 43 148-154
[4]  
Lowen SB(2001)Measuring the facial phenotype of individuals with prenatal alcohol exposure: correlations with brain dysfunction Alcohol and Alcoholism 36 147-159
[5]  
Renshaw PF(1977)The effect of ethanol chronically administered to preweanling rats on cerebellar development: a morphological study Brain Research 119 249-268
[6]  
Teicher MH(1999)Ethyl linoleate in meconium: a biomarker for prenatal ethanol exposure Alcoholism, Clinical and Experimental Research 23 487-493
[7]  
Archibald SL(2003)Validation of a new biomarker of fetal exposure to alcohol The Journal of Pediatrics 143 463-469
[8]  
Fennema-Notestine C(1998)Cerebellum in attention-deficit hyperactivity disorder: a morphometric MRI study Neurology 50 1087-1093
[9]  
Gamst A(2001)Ethanol exerts different effects on myelin basic protein and 2′,3′-cyclic nucleotide 3′-phosphodiesterase expression in differentiating CG-4 oligodendrocytes Brain Research. Developmental Brain Research 128 9-16
[10]  
Riley EP(1991)Permanent neuronal deficits in rats exposed to alcohol during the brain growth spurt Teratology 44 147-163