Interhemispheric transfer in children with heavy prenatal alcohol exposure

被引:35
作者
Roebuck, TM [1 ]
Mattson, SN [1 ]
Riley, EP [1 ]
机构
[1] San Diego State Univ, Ctr Behav Teratol, San Diego, CA 92120 USA
关键词
fetal alcohol syndrome; corpus callosum; interhemispheric transfer; prenatal alcohol exposure; finger localization;
D O I
10.1097/01.ALC.0000042219.73648.46
中图分类号
R194 [卫生标准、卫生检查、医药管理];
学科分类号
摘要
Background: Prenatal alcohol exposure has long been associated with alterations in brain structure and behavioral changes. The corpus callosum can be affected by heavy prenatal alcohol exposure, and agenesis (absence) of this structure occurs more often in children with fetal alcohol syndrome than in the general population or in other developmentally delayed populations. Although the majority of children with fetal alcohol syndrome do not have agenesis of the corpus callosum, callosal area is reduced in this population, particularly in the anterior and posterior regions. However, the functional implication of these size reductions has not been examined. Methods: The current study used a finger localization task to measure the transfer of information across the corpus callosum in children and adolescents with histories of heavy prenatal alcohol exposure and age and sex-matched controls. In a subset of children, correlational analysis was also conducted between behavioral data and cross-sectional area of the corpus callosum. Results: When compared with nonexposed controls, alcohol-exposed children made more errors on trials for which information had to cross the corpus callosum ("crossed" trials) than on trials for which it did not ("uncrossed" trials), and they also made more errors as the task increased in complexity. Additionally, correlations with magnetic resonance imaging data in a subset of children revealed that impairment in interhemispheric transfer was related to reductions in the size of the corpus callosum. These correlations were independent of effects expected from the relationship between corpus callosum size and general intellectual functioning alone. Conclusions: These findings suggest that children with heavy prenatal alcohol exposure display subtle deficits in the interhemispheric transfer of information in the somatosensory domain. Such deficits in interhemispheric transfer are likely to be related to the myriad of other behavioral and cognitive impairments observed in these children.
引用
收藏
页码:1863 / 1871
页数:9
相关论文
共 60 条
[1]  
[Anonymous], ALCOHOL BRAIN DEV
[2]   Brain dysmorphology in individuals with severe prenatal alcohol exposure [J].
Archibald, SL ;
Fennema-Notestine, C ;
Gamst, A ;
Riley, EP ;
Mattson, SN ;
Jernigan, TL .
DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY, 2001, 43 (03) :148-154
[3]  
Banich M.T., 1994, NEUROPSYCHOLOGY, V8, P263, DOI DOI 10.1037/0894-4105.8.2.263
[4]   The missing link: The role of interhemispheric interaction in attentional processing [J].
Banich, MT .
BRAIN AND COGNITION, 1998, 36 (02) :128-157
[5]  
BAYNES K, 1997, BEHAV NEUROLOGY NEUR, P419
[6]   Corpus callosum damage and interhemispheric transfer of information following closed head injury in children [J].
Benavidez, DA ;
Fletcher, JM ;
Hannay, HJ ;
Bland, ST ;
Caudle, SE ;
Mendelsohn, DB ;
Yeakley, J ;
Brunder, DG ;
Harward, H ;
Song, J ;
Perachio, NA ;
Bruce, D ;
Scheibel, RS ;
Lilly, MA ;
Verger-Maestre, K ;
Levin, HS .
CORTEX, 1999, 35 (03) :315-336
[7]   Geometric morphometrics of corpus callosum and subcortical structures in the fetal-alcohol-affected brain [J].
Bookstein, FL ;
Sampson, PD ;
Streissguth, AP ;
Connor, PD .
TERATOLOGY, 2001, 64 (01) :4-32
[8]   BRAIN MALFORMATIONS RELATED TO PRENATAL EXPOSURE TO ETHANOL [J].
CLARREN, SK ;
ALVORD, EC ;
SUMI, SM ;
STREISSGUTH, AP ;
SMITH, DW .
JOURNAL OF PEDIATRICS, 1978, 92 (01) :64-67
[9]   NEUROPSYCHOLOGICAL DEFICITS IN FETAL ALCOHOL SYNDROME AND FETAL ALCOHOL EFFECTS [J].
CONRY, J .
ALCOHOLISM-CLINICAL AND EXPERIMENTAL RESEARCH, 1990, 14 (05) :650-655
[10]   MIDLINE CEREBRAL DYSGENESIS, DYSFUNCTION OF THE HYPOTHALAMIC-PITUITARY AXIS, AND FETAL ALCOHOL EFFECTS [J].
COULTER, CL ;
LEECH, RW ;
SCHAEFER, GB ;
SCHEITHAUER, BW ;
BRUMBACK, RA .
ARCHIVES OF NEUROLOGY, 1993, 50 (07) :771-775