Cargando…

An fMRI investigation of neural activation predicting memory formation in children with fetal alcohol spectrum disorders

Prenatal alcohol exposure (PAE) is associated with physical anomalies, growth restriction, and a range of neurobehavioral deficits. Although declarative memory impairment has been documented extensively in individuals with fetal alcohol spectrum disorders (FASD), this cognitive process has been exam...

Descripción completa

Detalles Bibliográficos
Autores principales: Lewis, Catherine E., Thomas, Kevin G.F., Ofen, Noa, Warton, Christopher M.R., Robertson, Frances, Lindinger, Nadine M., Molteno, Christopher D., Meintjes, Ernesta M., Jacobson, Joseph L., Jacobson, Sandra W.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7918676/
https://www.ncbi.nlm.nih.gov/pubmed/33636539
http://dx.doi.org/10.1016/j.nicl.2020.102532
_version_ 1783657978388283392
author Lewis, Catherine E.
Thomas, Kevin G.F.
Ofen, Noa
Warton, Christopher M.R.
Robertson, Frances
Lindinger, Nadine M.
Molteno, Christopher D.
Meintjes, Ernesta M.
Jacobson, Joseph L.
Jacobson, Sandra W.
author_facet Lewis, Catherine E.
Thomas, Kevin G.F.
Ofen, Noa
Warton, Christopher M.R.
Robertson, Frances
Lindinger, Nadine M.
Molteno, Christopher D.
Meintjes, Ernesta M.
Jacobson, Joseph L.
Jacobson, Sandra W.
author_sort Lewis, Catherine E.
collection PubMed
description Prenatal alcohol exposure (PAE) is associated with physical anomalies, growth restriction, and a range of neurobehavioral deficits. Although declarative memory impairment has been documented extensively in individuals with fetal alcohol spectrum disorders (FASD), this cognitive process has been examined in only one functional magnetic resonance imaging (fMRI) study, and mechanisms underlying this impairment are not well understood. We used an event-related fMRI design to examine neural activations during visual scene encoding that predict subsequent scene memory in 51 right-handed children (age range = 10–14 years, M = 11.3, SD = 1.3) whose mothers had been recruited and interviewed prospectively about their alcohol use during pregnancy. Following examination by expert dysmorphologists, children were assigned to one of three FASD diagnostic groups: FAS/PFAS (n(FAS) = 7; n(PFAS) = 4), nonsyndromal heavily exposed (HE; n = 14), and Controls (n = 26). Subsequent memory was assessed in a post-scan recognition test, and subsequent memory activations were examined by contrasting activations during encoding of scenes that were subsequently remembered (hits) to those for incorrectly judged as ‘new’ (misses). Recognition accuracy did not differ between groups. Pooled across groups, we observed extensive bilateral subsequent memory effects in regions including the hippocampal formation, posterior parietal cortex, and occipital cortex—a pattern consistent with previous similar studies of typically developing children. Critically, in the group of children with FAS or PFAS, we observed activations in several additional regions compared to HE and Control groups. Given the absence of between-group differences in recognition accuracy, these data suggest that in achieving similar memory compared to children in the HE and Control groups, children with FAS and PFAS recruit more extensive neural resources to achieve successful memory formation.
format Online
Article
Text
id pubmed-7918676
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher Elsevier
record_format MEDLINE/PubMed
spelling pubmed-79186762021-03-05 An fMRI investigation of neural activation predicting memory formation in children with fetal alcohol spectrum disorders Lewis, Catherine E. Thomas, Kevin G.F. Ofen, Noa Warton, Christopher M.R. Robertson, Frances Lindinger, Nadine M. Molteno, Christopher D. Meintjes, Ernesta M. Jacobson, Joseph L. Jacobson, Sandra W. Neuroimage Clin Regular Article Prenatal alcohol exposure (PAE) is associated with physical anomalies, growth restriction, and a range of neurobehavioral deficits. Although declarative memory impairment has been documented extensively in individuals with fetal alcohol spectrum disorders (FASD), this cognitive process has been examined in only one functional magnetic resonance imaging (fMRI) study, and mechanisms underlying this impairment are not well understood. We used an event-related fMRI design to examine neural activations during visual scene encoding that predict subsequent scene memory in 51 right-handed children (age range = 10–14 years, M = 11.3, SD = 1.3) whose mothers had been recruited and interviewed prospectively about their alcohol use during pregnancy. Following examination by expert dysmorphologists, children were assigned to one of three FASD diagnostic groups: FAS/PFAS (n(FAS) = 7; n(PFAS) = 4), nonsyndromal heavily exposed (HE; n = 14), and Controls (n = 26). Subsequent memory was assessed in a post-scan recognition test, and subsequent memory activations were examined by contrasting activations during encoding of scenes that were subsequently remembered (hits) to those for incorrectly judged as ‘new’ (misses). Recognition accuracy did not differ between groups. Pooled across groups, we observed extensive bilateral subsequent memory effects in regions including the hippocampal formation, posterior parietal cortex, and occipital cortex—a pattern consistent with previous similar studies of typically developing children. Critically, in the group of children with FAS or PFAS, we observed activations in several additional regions compared to HE and Control groups. Given the absence of between-group differences in recognition accuracy, these data suggest that in achieving similar memory compared to children in the HE and Control groups, children with FAS and PFAS recruit more extensive neural resources to achieve successful memory formation. Elsevier 2020-12-11 /pmc/articles/PMC7918676/ /pubmed/33636539 http://dx.doi.org/10.1016/j.nicl.2020.102532 Text en © 2020 The Author(s) http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Regular Article
Lewis, Catherine E.
Thomas, Kevin G.F.
Ofen, Noa
Warton, Christopher M.R.
Robertson, Frances
Lindinger, Nadine M.
Molteno, Christopher D.
Meintjes, Ernesta M.
Jacobson, Joseph L.
Jacobson, Sandra W.
An fMRI investigation of neural activation predicting memory formation in children with fetal alcohol spectrum disorders
title An fMRI investigation of neural activation predicting memory formation in children with fetal alcohol spectrum disorders
title_full An fMRI investigation of neural activation predicting memory formation in children with fetal alcohol spectrum disorders
title_fullStr An fMRI investigation of neural activation predicting memory formation in children with fetal alcohol spectrum disorders
title_full_unstemmed An fMRI investigation of neural activation predicting memory formation in children with fetal alcohol spectrum disorders
title_short An fMRI investigation of neural activation predicting memory formation in children with fetal alcohol spectrum disorders
title_sort fmri investigation of neural activation predicting memory formation in children with fetal alcohol spectrum disorders
topic Regular Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7918676/
https://www.ncbi.nlm.nih.gov/pubmed/33636539
http://dx.doi.org/10.1016/j.nicl.2020.102532
work_keys_str_mv AT lewiscatherinee anfmriinvestigationofneuralactivationpredictingmemoryformationinchildrenwithfetalalcoholspectrumdisorders
AT thomaskevingf anfmriinvestigationofneuralactivationpredictingmemoryformationinchildrenwithfetalalcoholspectrumdisorders
AT ofennoa anfmriinvestigationofneuralactivationpredictingmemoryformationinchildrenwithfetalalcoholspectrumdisorders
AT wartonchristophermr anfmriinvestigationofneuralactivationpredictingmemoryformationinchildrenwithfetalalcoholspectrumdisorders
AT robertsonfrances anfmriinvestigationofneuralactivationpredictingmemoryformationinchildrenwithfetalalcoholspectrumdisorders
AT lindingernadinem anfmriinvestigationofneuralactivationpredictingmemoryformationinchildrenwithfetalalcoholspectrumdisorders
AT moltenochristopherd anfmriinvestigationofneuralactivationpredictingmemoryformationinchildrenwithfetalalcoholspectrumdisorders
AT meintjesernestam anfmriinvestigationofneuralactivationpredictingmemoryformationinchildrenwithfetalalcoholspectrumdisorders
AT jacobsonjosephl anfmriinvestigationofneuralactivationpredictingmemoryformationinchildrenwithfetalalcoholspectrumdisorders
AT jacobsonsandraw anfmriinvestigationofneuralactivationpredictingmemoryformationinchildrenwithfetalalcoholspectrumdisorders
AT lewiscatherinee fmriinvestigationofneuralactivationpredictingmemoryformationinchildrenwithfetalalcoholspectrumdisorders
AT thomaskevingf fmriinvestigationofneuralactivationpredictingmemoryformationinchildrenwithfetalalcoholspectrumdisorders
AT ofennoa fmriinvestigationofneuralactivationpredictingmemoryformationinchildrenwithfetalalcoholspectrumdisorders
AT wartonchristophermr fmriinvestigationofneuralactivationpredictingmemoryformationinchildrenwithfetalalcoholspectrumdisorders
AT robertsonfrances fmriinvestigationofneuralactivationpredictingmemoryformationinchildrenwithfetalalcoholspectrumdisorders
AT lindingernadinem fmriinvestigationofneuralactivationpredictingmemoryformationinchildrenwithfetalalcoholspectrumdisorders
AT moltenochristopherd fmriinvestigationofneuralactivationpredictingmemoryformationinchildrenwithfetalalcoholspectrumdisorders
AT meintjesernestam fmriinvestigationofneuralactivationpredictingmemoryformationinchildrenwithfetalalcoholspectrumdisorders
AT jacobsonjosephl fmriinvestigationofneuralactivationpredictingmemoryformationinchildrenwithfetalalcoholspectrumdisorders
AT jacobsonsandraw fmriinvestigationofneuralactivationpredictingmemoryformationinchildrenwithfetalalcoholspectrumdisorders