Delays in Auditory Processing Identified in Preschool Children with FASD
Background Both sensory and cognitive deficits have been associated with prenatal exposure to alcohol; however, very few studies have focused on sensory deficits in preschool‐aged children. As sensory skills develop early, characterization of sensory deficits using novel imaging methods may reveal i...
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Published in | Alcoholism, clinical and experimental research Vol. 36; no. 10; pp. 1720 - 1727 |
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Main Authors | , , , , , , , |
Format | Journal Article |
Language | English |
Published |
Hoboken, NJ
Blackwell Publishing Ltd
01.10.2012
Wiley |
Subjects | |
Online Access | Get full text |
ISSN | 0145-6008 1530-0277 1530-0277 |
DOI | 10.1111/j.1530-0277.2012.01769.x |
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Abstract | Background
Both sensory and cognitive deficits have been associated with prenatal exposure to alcohol; however, very few studies have focused on sensory deficits in preschool‐aged children. As sensory skills develop early, characterization of sensory deficits using novel imaging methods may reveal important neural markers of prenatal alcohol exposure.
Methods
Participants in this study were 10 children with a fetal alcohol spectrum disorder (FASD) and 15 healthy control (HC) children aged 3 to 6 years. All participants had normal hearing as determined by clinical screens. We measured their neurophysiological responses to auditory stimuli (1,000 Hz, 72 dB tone) using magnetoencephalography (MEG). We used a multidipole spatio‐temporal modeling technique to identify the location and timecourse of cortical activity in response to the auditory tones. The timing and amplitude of the left and right superior temporal gyrus sources associated with activation of left and right primary/secondary auditory cortices were compared across groups.
Results
There was a significant delay in M100 and M200 latencies for the FASD children relative to the HC children (p = 0.01), when including age as a covariate. The within‐subjects effect of hemisphere was not significant. A comparable delay in M100 and M200 latencies was observed in children across the FASD subtypes.
Conclusions
Auditory delay revealed by MEG in children with FASDs may prove to be a useful neural marker of information processing difficulties in young children with prenatal alcohol exposure. The fact that delayed auditory responses were observed across the FASD spectrum suggests that it may be a sensitive measure of alcohol‐induced brain damage. Therefore, this measure in conjunction with other clinical tools may prove useful for early identification of alcohol affected children, particularly those without dysmorphia. |
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AbstractList | Both sensory and cognitive deficits have been associated with prenatal exposure to alcohol; however, very few studies have focused on sensory deficits in preschool-aged children. As sensory skills develop early, characterization of sensory deficits using novel imaging methods may reveal important neural markers of prenatal alcohol exposure.
Participants in this study were 10 children with a fetal alcohol spectrum disorder (FASD) and 15 healthy control (HC) children aged 3 to 6 years. All participants had normal hearing as determined by clinical screens. We measured their neurophysiological responses to auditory stimuli (1,000 Hz, 72 dB tone) using magnetoencephalography (MEG). We used a multidipole spatio-temporal modeling technique to identify the location and timecourse of cortical activity in response to the auditory tones. The timing and amplitude of the left and right superior temporal gyrus sources associated with activation of left and right primary/secondary auditory cortices were compared across groups.
There was a significant delay in M100 and M200 latencies for the FASD children relative to the HC children (p = 0.01), when including age as a covariate. The within-subjects effect of hemisphere was not significant. A comparable delay in M100 and M200 latencies was observed in children across the FASD subtypes.
Auditory delay revealed by MEG in children with FASDs may prove to be a useful neural marker of information processing difficulties in young children with prenatal alcohol exposure. The fact that delayed auditory responses were observed across the FASD spectrum suggests that it may be a sensitive measure of alcohol-induced brain damage. Therefore, this measure in conjunction with other clinical tools may prove useful for early identification of alcohol affected children, particularly those without dysmorphia. Background Both sensory and cognitive deficits have been associated with prenatal exposure to alcohol; however, very few studies have focused on sensory deficits in preschool‐aged children. As sensory skills develop early, characterization of sensory deficits using novel imaging methods may reveal important neural markers of prenatal alcohol exposure. Methods Participants in this study were 10 children with a fetal alcohol spectrum disorder (FASD) and 15 healthy control (HC) children aged 3 to 6 years. All participants had normal hearing as determined by clinical screens. We measured their neurophysiological responses to auditory stimuli (1,000 Hz, 72 dB tone) using magnetoencephalography (MEG). We used a multidipole spatio‐temporal modeling technique to identify the location and timecourse of cortical activity in response to the auditory tones. The timing and amplitude of the left and right superior temporal gyrus sources associated with activation of left and right primary/secondary auditory cortices were compared across groups. Results There was a significant delay in M100 and M200 latencies for the FASD children relative to the HC children (p = 0.01), when including age as a covariate. The within‐subjects effect of hemisphere was not significant. A comparable delay in M100 and M200 latencies was observed in children across the FASD subtypes. Conclusions Auditory delay revealed by MEG in children with FASDs may prove to be a useful neural marker of information processing difficulties in young children with prenatal alcohol exposure. The fact that delayed auditory responses were observed across the FASD spectrum suggests that it may be a sensitive measure of alcohol‐induced brain damage. Therefore, this measure in conjunction with other clinical tools may prove useful for early identification of alcohol affected children, particularly those without dysmorphia. Both sensory and cognitive deficits have been associated with prenatal exposure to alcohol; however, very few studies have focused on sensory deficits in preschool-aged children. As sensory skills develop early, characterization of sensory deficits using novel imaging methods may reveal important neural markers of prenatal alcohol exposure.BACKGROUNDBoth sensory and cognitive deficits have been associated with prenatal exposure to alcohol; however, very few studies have focused on sensory deficits in preschool-aged children. As sensory skills develop early, characterization of sensory deficits using novel imaging methods may reveal important neural markers of prenatal alcohol exposure.Participants in this study were 10 children with a fetal alcohol spectrum disorder (FASD) and 15 healthy control (HC) children aged 3 to 6 years. All participants had normal hearing as determined by clinical screens. We measured their neurophysiological responses to auditory stimuli (1,000 Hz, 72 dB tone) using magnetoencephalography (MEG). We used a multidipole spatio-temporal modeling technique to identify the location and timecourse of cortical activity in response to the auditory tones. The timing and amplitude of the left and right superior temporal gyrus sources associated with activation of left and right primary/secondary auditory cortices were compared across groups.METHODSParticipants in this study were 10 children with a fetal alcohol spectrum disorder (FASD) and 15 healthy control (HC) children aged 3 to 6 years. All participants had normal hearing as determined by clinical screens. We measured their neurophysiological responses to auditory stimuli (1,000 Hz, 72 dB tone) using magnetoencephalography (MEG). We used a multidipole spatio-temporal modeling technique to identify the location and timecourse of cortical activity in response to the auditory tones. The timing and amplitude of the left and right superior temporal gyrus sources associated with activation of left and right primary/secondary auditory cortices were compared across groups.There was a significant delay in M100 and M200 latencies for the FASD children relative to the HC children (p = 0.01), when including age as a covariate. The within-subjects effect of hemisphere was not significant. A comparable delay in M100 and M200 latencies was observed in children across the FASD subtypes.RESULTSThere was a significant delay in M100 and M200 latencies for the FASD children relative to the HC children (p = 0.01), when including age as a covariate. The within-subjects effect of hemisphere was not significant. A comparable delay in M100 and M200 latencies was observed in children across the FASD subtypes.Auditory delay revealed by MEG in children with FASDs may prove to be a useful neural marker of information processing difficulties in young children with prenatal alcohol exposure. The fact that delayed auditory responses were observed across the FASD spectrum suggests that it may be a sensitive measure of alcohol-induced brain damage. Therefore, this measure in conjunction with other clinical tools may prove useful for early identification of alcohol affected children, particularly those without dysmorphia.CONCLUSIONSAuditory delay revealed by MEG in children with FASDs may prove to be a useful neural marker of information processing difficulties in young children with prenatal alcohol exposure. The fact that delayed auditory responses were observed across the FASD spectrum suggests that it may be a sensitive measure of alcohol-induced brain damage. Therefore, this measure in conjunction with other clinical tools may prove useful for early identification of alcohol affected children, particularly those without dysmorphia. |
Author | Peters, Amanda M. Kodituwakku, Elizabeth L. Stephen, Julia M. Romero, Lucinda Kodituwakku, Piyadasa W. Caprihan, Arvind Coffman, Brian A. Sharadamma, Nirupama M. |
AuthorAffiliation | 2 Department of Pediatrics, University of New Mexico Health Sciences Center, Albuquerque, NM 87131 3 Department of Psychology, University of New Mexico, Albuquerque, NM 87131 1 The Mind Research Network, Albuquerque, NM, 87106 |
AuthorAffiliation_xml | – name: 2 Department of Pediatrics, University of New Mexico Health Sciences Center, Albuquerque, NM 87131 – name: 1 The Mind Research Network, Albuquerque, NM, 87106 – name: 3 Department of Psychology, University of New Mexico, Albuquerque, NM 87131 |
Author_xml | – sequence: 1 givenname: Julia M. surname: Stephen fullname: Stephen, Julia M. email: jstephen@mrn.org organization: Mind Research Network, New Mexico, Albuquerque – sequence: 2 givenname: Piyadasa W. surname: Kodituwakku fullname: Kodituwakku, Piyadasa W. organization: Department of Pediatrics, University of New Mexico Health Sciences Center, New Mexico, Albuquerque – sequence: 3 givenname: Elizabeth L. surname: Kodituwakku fullname: Kodituwakku, Elizabeth L. organization: Department of Pediatrics, University of New Mexico Health Sciences Center, New Mexico, Albuquerque – sequence: 4 givenname: Lucinda surname: Romero fullname: Romero, Lucinda organization: Mind Research Network, New Mexico, Albuquerque – sequence: 5 givenname: Amanda M. surname: Peters fullname: Peters, Amanda M. organization: Mind Research Network, New Mexico, Albuquerque – sequence: 6 givenname: Nirupama M. surname: Sharadamma fullname: Sharadamma, Nirupama M. organization: Mind Research Network, New Mexico, Albuquerque – sequence: 7 givenname: Arvind surname: Caprihan fullname: Caprihan, Arvind organization: Mind Research Network, New Mexico, Albuquerque – sequence: 8 givenname: Brian A. surname: Coffman fullname: Coffman, Brian A. organization: Mind Research Network, Albuquerque, New Mexico |
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Keywords | Human Preschool age Fetal alcohol syndrome Ethanol Magnetoencephalography Fetal Alcohol Spectrum Disorders Time lag Newborn diseases Hearing Auditory Information processing Child Preschool Children |
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Both sensory and cognitive deficits have been associated with prenatal exposure to alcohol; however, very few studies have focused on sensory... Both sensory and cognitive deficits have been associated with prenatal exposure to alcohol; however, very few studies have focused on sensory deficits in... |
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SubjectTerms | Acoustic Stimulation - methods Alcoholism and acute alcohol poisoning Auditory Auditory Perceptual Disorders - diagnosis Auditory Perceptual Disorders - epidemiology Auditory Perceptual Disorders - physiopathology Biological and medical sciences Child Child, Preschool Female Fetal Alcohol Spectrum Disorders Fetal Alcohol Spectrum Disorders - diagnosis Fetal Alcohol Spectrum Disorders - epidemiology Fetal Alcohol Spectrum Disorders - physiopathology Humans Magnetoencephalography Magnetoencephalography - methods Male Medical sciences Pregnancy Preschool Children Reaction Time - physiology Toxicology |
Title | Delays in Auditory Processing Identified in Preschool Children with FASD |
URI | https://api.istex.fr/ark:/67375/WNG-FLZHXPK6-P/fulltext.pdf https://onlinelibrary.wiley.com/doi/abs/10.1111%2Fj.1530-0277.2012.01769.x https://www.ncbi.nlm.nih.gov/pubmed/22458372 https://www.proquest.com/docview/1082237075 https://pubmed.ncbi.nlm.nih.gov/PMC3390452 |
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