Delayed Mismatch Field Latencies in Autism Spectrum Disorder with Abnormal Auditory Sensitivity: A Magnetoencephalographic Study

Although abnormal auditory sensitivity is the most common sensory impairment associated with autism spectrum disorder (ASD), the neurophysiological mechanisms remain unknown. In previous studies, we reported that this abnormal sensitivity in patients with ASD is associated with delayed and prolonged...

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Main Authors: Junko Matsuzaki, Kuriko Kagitani-Shimono, Hisato Sugata, Ryuzo Hanaie, Fumiyo Nagatani, Tomoka Yamamoto, Masaya Tachibana, Koji Tominaga, Masayuki Hirata, Ikuko Mohri, Masako Taniike
Format: Article
Language:English
Published: Frontiers Media S.A. 2017-09-01
Series:Frontiers in Human Neuroscience
Subjects:
Online Access:http://journal.frontiersin.org/article/10.3389/fnhum.2017.00446/full
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language English
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author Junko Matsuzaki
Junko Matsuzaki
Junko Matsuzaki
Kuriko Kagitani-Shimono
Kuriko Kagitani-Shimono
Kuriko Kagitani-Shimono
Hisato Sugata
Ryuzo Hanaie
Ryuzo Hanaie
Fumiyo Nagatani
Tomoka Yamamoto
Masaya Tachibana
Masaya Tachibana
Masaya Tachibana
Koji Tominaga
Koji Tominaga
Masayuki Hirata
Masayuki Hirata
Ikuko Mohri
Ikuko Mohri
Ikuko Mohri
Masako Taniike
Masako Taniike
Masako Taniike
spellingShingle Junko Matsuzaki
Junko Matsuzaki
Junko Matsuzaki
Kuriko Kagitani-Shimono
Kuriko Kagitani-Shimono
Kuriko Kagitani-Shimono
Hisato Sugata
Ryuzo Hanaie
Ryuzo Hanaie
Fumiyo Nagatani
Tomoka Yamamoto
Masaya Tachibana
Masaya Tachibana
Masaya Tachibana
Koji Tominaga
Koji Tominaga
Masayuki Hirata
Masayuki Hirata
Ikuko Mohri
Ikuko Mohri
Ikuko Mohri
Masako Taniike
Masako Taniike
Masako Taniike
Delayed Mismatch Field Latencies in Autism Spectrum Disorder with Abnormal Auditory Sensitivity: A Magnetoencephalographic Study
Frontiers in Human Neuroscience
autism spectrum disorders (ASD)
abnormal auditory sensitivity
mismatch fields
magnetoencephalography (MEG)
oddball paradigm
author_facet Junko Matsuzaki
Junko Matsuzaki
Junko Matsuzaki
Kuriko Kagitani-Shimono
Kuriko Kagitani-Shimono
Kuriko Kagitani-Shimono
Hisato Sugata
Ryuzo Hanaie
Ryuzo Hanaie
Fumiyo Nagatani
Tomoka Yamamoto
Masaya Tachibana
Masaya Tachibana
Masaya Tachibana
Koji Tominaga
Koji Tominaga
Masayuki Hirata
Masayuki Hirata
Ikuko Mohri
Ikuko Mohri
Ikuko Mohri
Masako Taniike
Masako Taniike
Masako Taniike
author_sort Junko Matsuzaki
title Delayed Mismatch Field Latencies in Autism Spectrum Disorder with Abnormal Auditory Sensitivity: A Magnetoencephalographic Study
title_short Delayed Mismatch Field Latencies in Autism Spectrum Disorder with Abnormal Auditory Sensitivity: A Magnetoencephalographic Study
title_full Delayed Mismatch Field Latencies in Autism Spectrum Disorder with Abnormal Auditory Sensitivity: A Magnetoencephalographic Study
title_fullStr Delayed Mismatch Field Latencies in Autism Spectrum Disorder with Abnormal Auditory Sensitivity: A Magnetoencephalographic Study
title_full_unstemmed Delayed Mismatch Field Latencies in Autism Spectrum Disorder with Abnormal Auditory Sensitivity: A Magnetoencephalographic Study
title_sort delayed mismatch field latencies in autism spectrum disorder with abnormal auditory sensitivity: a magnetoencephalographic study
publisher Frontiers Media S.A.
series Frontiers in Human Neuroscience
issn 1662-5161
publishDate 2017-09-01
description Although abnormal auditory sensitivity is the most common sensory impairment associated with autism spectrum disorder (ASD), the neurophysiological mechanisms remain unknown. In previous studies, we reported that this abnormal sensitivity in patients with ASD is associated with delayed and prolonged responses in the auditory cortex. In the present study, we investigated alterations in residual M100 and MMFs in children with ASD who experience abnormal auditory sensitivity. We used magnetoencephalography (MEG) to measure MMF elicited by an auditory oddball paradigm (standard tones: 300 Hz, deviant tones: 700 Hz) in 20 boys with ASD (11 with abnormal auditory sensitivity: mean age, 9.62 ± 1.82 years, 9 without: mean age, 9.07 ± 1.31 years) and 13 typically developing boys (mean age, 9.45 ± 1.51 years). We found that temporal and frontal residual M100/MMF latencies were significantly longer only in children with ASD who have abnormal auditory sensitivity. In addition, prolonged residual M100/MMF latencies were correlated with the severity of abnormal auditory sensitivity in temporal and frontal areas of both hemispheres. Therefore, our findings suggest that children with ASD and abnormal auditory sensitivity may have atypical neural networks in the primary auditory area, as well as in brain areas associated with attention switching and inhibitory control processing. This is the first report of an MEG study demonstrating altered MMFs to an auditory oddball paradigm in patients with ASD and abnormal auditory sensitivity. These findings contribute to knowledge of the mechanisms for abnormal auditory sensitivity in ASD, and may therefore facilitate development of novel clinical interventions.
topic autism spectrum disorders (ASD)
abnormal auditory sensitivity
mismatch fields
magnetoencephalography (MEG)
oddball paradigm
url http://journal.frontiersin.org/article/10.3389/fnhum.2017.00446/full
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spelling doaj-239d488f7aaf48c29725ea207d3f30a82020-11-25T02:19:28ZengFrontiers Media S.A.Frontiers in Human Neuroscience1662-51612017-09-011110.3389/fnhum.2017.00446259353Delayed Mismatch Field Latencies in Autism Spectrum Disorder with Abnormal Auditory Sensitivity: A Magnetoencephalographic StudyJunko Matsuzaki0Junko Matsuzaki1Junko Matsuzaki2Kuriko Kagitani-Shimono3Kuriko Kagitani-Shimono4Kuriko Kagitani-Shimono5Hisato Sugata6Ryuzo Hanaie7Ryuzo Hanaie8Fumiyo Nagatani9Tomoka Yamamoto10Masaya Tachibana11Masaya Tachibana12Masaya Tachibana13Koji Tominaga14Koji Tominaga15Masayuki Hirata16Masayuki Hirata17Ikuko Mohri18Ikuko Mohri19Ikuko Mohri20Masako Taniike21Masako Taniike22Masako Taniike23Molecular Research Center for Children's Mental Development, United Graduate School of Child Development, Osaka University Graduate School of MedicineOsaka, JapanDivision of Developmental Neuroscience, United Graduate School of Child Development, Osaka University Graduate School of MedicineOsaka, JapanDepartment of Pediatrics, Osaka University Graduate School of MedicineOsaka, JapanMolecular Research Center for Children's Mental Development, United Graduate School of Child Development, Osaka University Graduate School of MedicineOsaka, JapanDivision of Developmental Neuroscience, United Graduate School of Child Development, Osaka University Graduate School of MedicineOsaka, JapanDepartment of Pediatrics, Osaka University Graduate School of MedicineOsaka, JapanDepartment of Neurosurgery, Osaka University Graduate School of MedicineOsaka, JapanMolecular Research Center for Children's Mental Development, United Graduate School of Child Development, Osaka University Graduate School of MedicineOsaka, JapanDivision of Developmental Neuroscience, United Graduate School of Child Development, Osaka University Graduate School of MedicineOsaka, JapanMolecular Research Center for Children's Mental Development, United Graduate School of Child Development, Osaka University Graduate School of MedicineOsaka, JapanMolecular Research Center for Children's Mental Development, United Graduate School of Child Development, Osaka University Graduate School of MedicineOsaka, JapanMolecular Research Center for Children's Mental Development, United Graduate School of Child Development, Osaka University Graduate School of MedicineOsaka, JapanDivision of Developmental Neuroscience, United Graduate School of Child Development, Osaka University Graduate School of MedicineOsaka, JapanDepartment of Pediatrics, Osaka University Graduate School of MedicineOsaka, JapanDivision of Developmental Neuroscience, United Graduate School of Child Development, Osaka University Graduate School of MedicineOsaka, JapanDepartment of Pediatrics, Osaka University Graduate School of MedicineOsaka, JapanDepartment of Neurosurgery, Osaka University Graduate School of MedicineOsaka, JapanEndowed Research Department of Clinical Neuroengineering, Global Center for Medical Engineering and Informatics, Osaka UniversityOsaka, JapanMolecular Research Center for Children's Mental Development, United Graduate School of Child Development, Osaka University Graduate School of MedicineOsaka, JapanDivision of Developmental Neuroscience, United Graduate School of Child Development, Osaka University Graduate School of MedicineOsaka, JapanDepartment of Pediatrics, Osaka University Graduate School of MedicineOsaka, JapanMolecular Research Center for Children's Mental Development, United Graduate School of Child Development, Osaka University Graduate School of MedicineOsaka, JapanDivision of Developmental Neuroscience, United Graduate School of Child Development, Osaka University Graduate School of MedicineOsaka, JapanDepartment of Pediatrics, Osaka University Graduate School of MedicineOsaka, JapanAlthough abnormal auditory sensitivity is the most common sensory impairment associated with autism spectrum disorder (ASD), the neurophysiological mechanisms remain unknown. In previous studies, we reported that this abnormal sensitivity in patients with ASD is associated with delayed and prolonged responses in the auditory cortex. In the present study, we investigated alterations in residual M100 and MMFs in children with ASD who experience abnormal auditory sensitivity. We used magnetoencephalography (MEG) to measure MMF elicited by an auditory oddball paradigm (standard tones: 300 Hz, deviant tones: 700 Hz) in 20 boys with ASD (11 with abnormal auditory sensitivity: mean age, 9.62 ± 1.82 years, 9 without: mean age, 9.07 ± 1.31 years) and 13 typically developing boys (mean age, 9.45 ± 1.51 years). We found that temporal and frontal residual M100/MMF latencies were significantly longer only in children with ASD who have abnormal auditory sensitivity. In addition, prolonged residual M100/MMF latencies were correlated with the severity of abnormal auditory sensitivity in temporal and frontal areas of both hemispheres. Therefore, our findings suggest that children with ASD and abnormal auditory sensitivity may have atypical neural networks in the primary auditory area, as well as in brain areas associated with attention switching and inhibitory control processing. This is the first report of an MEG study demonstrating altered MMFs to an auditory oddball paradigm in patients with ASD and abnormal auditory sensitivity. These findings contribute to knowledge of the mechanisms for abnormal auditory sensitivity in ASD, and may therefore facilitate development of novel clinical interventions.http://journal.frontiersin.org/article/10.3389/fnhum.2017.00446/fullautism spectrum disorders (ASD)abnormal auditory sensitivitymismatch fieldsmagnetoencephalography (MEG)oddball paradigm