Literature DB >> 35187666

Compromised interhemispheric transfer of information partially mediates cognitive function deficits in adolescents with fetal alcohol syndrome.

Stevie C Biffen1, Neil C Dodge2, Christopher M R Warton3, Christopher D Molteno4, Joseph L Jacobson2,3,4, Ernesta M Meintjes1,5,6, Sandra W Jacobson2,3,4.   

Abstract

BACKGROUND: Prenatal alcohol exposure (PAE) has been associated with compromised interhemispheric transfer of tactile stimuli in childhood and structural changes to the corpus callosum (CC). In this study, we used a finger localization task (FLT) to investigate whether interhemispheric transfer deficits persist in adolescence; whether effects of PAE on perceptual reasoning, working memory, and executive function are mediated by deficits in interhemispheric transfer of information; and whether CC size in childhood predicts FLT performance in adolescence.
METHODS: Participants, aged 16 to 17 years, were from the Cape Town Longitudinal Cohort, whose mothers were recruited during pregnancy and interviewed regarding their alcohol use using the timeline follow-back method. Diagnoses of fetal alcohol syndrome (FAS) and partial FAS (PFAS) were determined by two expert dysmorphologists; nonsyndromal exposed children were designated as heavily exposed (HE); those born to abstainers or light drinkers, as controls. The FLT was administered to 74 participants (12 FAS, 16 PFAS, 14 HE and 32 controls). CC size at age 9 to 12 years was available for 35 participants (7 FAS, 13 PFAS, 5 HE and 10 control).
RESULTS: Although the degree of PAE was similar in the FAS, PFAS, and HE groups, only the adolescents with FAS showed more transfer-related errors than controls in conditions in which one finger was stimulated. FLT performance mediated the effects of FAS on perceptual reasoning and executive function. In the subsample for which neuroimaging data from childhood were available, there was an association among adolescents with PAE of smaller CC volumes with more transfer-related errors on the one-finger/hand hidden condition, suggesting that CC damage previously seen in childhood continues to impact function through adolescence.
CONCLUSIONS: This study provides evidence of compromised interhemispheric transfer of information in adolescents with FAS, while those with PFAS or heavy exposed nonsyndromal individuals are apparently spared. It is the first to show that PAE effects on important aspects of cognitive function are partially mediated by deficits in the interhemispheric transfer of information.
© 2022 by the Research Society on Alcoholism.

Entities:  

Keywords:  corpus callosum size; fetal alcohol syndrome; finger localization test; interhemispheric transfer; prenatal alcohol exposure

Mesh:

Substances:

Year:  2022        PMID: 35187666      PMCID: PMC9018477          DOI: 10.1111/acer.14795

Source DB:  PubMed          Journal:  Alcohol Clin Exp Res        ISSN: 0145-6008            Impact factor:   3.928


  58 in total

1.  Brain morphometry with multiecho MPRAGE.

Authors:  André J W van der Kouwe; Thomas Benner; David H Salat; Bruce Fischl
Journal:  Neuroimage       Date:  2008-02-01       Impact factor: 6.556

2.  Recognition of the fetal alcohol syndrome in early infancy.

Authors:  K L Jones; D W Smith
Journal:  Lancet       Date:  1973-11-03       Impact factor: 79.321

Review 3.  The association of mild, moderate, and binge prenatal alcohol exposure and child neuropsychological outcomes: a meta-analysis.

Authors:  Audrey L Flak; Su Su; Jacquelyn Bertrand; Clark H Denny; Ulrik S Kesmodel; Mary E Cogswell
Journal:  Alcohol Clin Exp Res       Date:  2013-08-01       Impact factor: 3.455

4.  Corpus callosum morphology in attention deficit-hyperactivity disorder: morphometric analysis of MRI.

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Journal:  J Learn Disabil       Date:  1991-03

5.  Inter-hemispheric functional connectivity disruption in children with prenatal alcohol exposure.

Authors:  Jeffrey R Wozniak; Bryon A Mueller; Ryan L Muetzel; Christopher J Bell; Heather L Hoecker; Miranda L Nelson; Pi-Nian Chang; Kelvin O Lim
Journal:  Alcohol Clin Exp Res       Date:  2011-02-08       Impact factor: 3.455

6.  Validation of a new biomarker of fetal exposure to alcohol.

Authors:  Cynthia F Bearer; Joseph L Jacobson; Sandra W Jacobson; Dana Barr; Julie Croxford; Christopher D Molteno; Denis L Viljoen; Anna-Susan Marais; Lisa M Chiodo; Andrew S Cwik
Journal:  J Pediatr       Date:  2003-10       Impact factor: 4.406

7.  Maternal risk factors for fetal alcohol syndrome and partial fetal alcohol syndrome in South Africa: a third study.

Authors:  Philip A May; J Phillip Gossage; Anna-Susan Marais; Loretta S Hendricks; Cudore L Snell; Barbara G Tabachnick; Chandra Stellavato; David G Buckley; Lesley E Brooke; Denis L Viljoen
Journal:  Alcohol Clin Exp Res       Date:  2008-03-11       Impact factor: 3.455

8.  A longitudinal study of the long-term consequences of drinking during pregnancy: heavy in utero alcohol exposure disrupts the normal processes of brain development.

Authors:  Catherine Lebel; Sarah N Mattson; Edward P Riley; Kenneth L Jones; Colleen M Adnams; Philip A May; Susan Y Bookheimer; Mary J O'Connor; Katherine L Narr; Eric Kan; Zvart Abaryan; Elizabeth R Sowell
Journal:  J Neurosci       Date:  2012-10-31       Impact factor: 6.167

9.  Reaction time measures of interhemispheric transfer time in reading disabled and normal children.

Authors:  R J Davidson; S C Leslie; C Saron
Journal:  Neuropsychologia       Date:  1990       Impact factor: 3.139

Review 10.  Neurobehavioral, neurologic, and neuroimaging characteristics of fetal alcohol spectrum disorders.

Authors:  Leila Glass; Ashley L Ware; Sarah N Mattson
Journal:  Handb Clin Neurol       Date:  2014
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