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Prolonged Auditory Brainstem Response in Universal Hearing Screening of Newborns with Autism Spectrum Disorder

Previous studies report prolonged auditory brainstem response (ABR) in children and adults with autism spectrum disorder (ASD). Despite its promise as a biomarker, it is unclear whether healthy newborns who later develop ASD also show ABR abnormalities. In the current study, we extracted ABR data on...

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Autores principales: Miron, Oren, Delgado, Rafael E., Delgado, Christine F., Simpson, Elizabeth A., Yu, Kun‐Hsing, Gutierrez, Anibal, Zeng, Guangyu, Gerstenberger, Jillian N., Kohane, Isaac S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons, Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7894135/
https://www.ncbi.nlm.nih.gov/pubmed/33140578
http://dx.doi.org/10.1002/aur.2422
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author Miron, Oren
Delgado, Rafael E.
Delgado, Christine F.
Simpson, Elizabeth A.
Yu, Kun‐Hsing
Gutierrez, Anibal
Zeng, Guangyu
Gerstenberger, Jillian N.
Kohane, Isaac S.
author_facet Miron, Oren
Delgado, Rafael E.
Delgado, Christine F.
Simpson, Elizabeth A.
Yu, Kun‐Hsing
Gutierrez, Anibal
Zeng, Guangyu
Gerstenberger, Jillian N.
Kohane, Isaac S.
author_sort Miron, Oren
collection PubMed
description Previous studies report prolonged auditory brainstem response (ABR) in children and adults with autism spectrum disorder (ASD). Despite its promise as a biomarker, it is unclear whether healthy newborns who later develop ASD also show ABR abnormalities. In the current study, we extracted ABR data on 139,154 newborns from their Universal Newborn Hearing Screening, including 321 newborns who were later diagnosed with ASD. We found that the ASD newborns had significant prolongations of their ABR phase and V‐negative latency compared with the non‐ASD newborns. Newborns in the ASD group also exhibited greater variance in their latencies compared to previous studies in older ASD samples, likely due in part to the low intensity of the ABR stimulus. These findings suggest that newborns display neurophysiological variation associated with ASD at birth. Future studies with higher‐intensity stimulus ABRs may allow more accurate predictions of ASD risk, which could augment the universal ABR test that currently screens millions of newborns worldwide. LAY SUMMARY: Children with autism spectrum disorder (ASD) have slow brain responses to sounds. We examined these brain responses from newborns' hearing tests and found that newborns who were later diagnosed with autism also had slower brain responses to sounds. Future studies might use these findings to better predict autism risk, with a hearing test that is already used on millions of newborns worldwide.
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spelling pubmed-78941352021-03-02 Prolonged Auditory Brainstem Response in Universal Hearing Screening of Newborns with Autism Spectrum Disorder Miron, Oren Delgado, Rafael E. Delgado, Christine F. Simpson, Elizabeth A. Yu, Kun‐Hsing Gutierrez, Anibal Zeng, Guangyu Gerstenberger, Jillian N. Kohane, Isaac S. Autism Res NEUROIMAGING Previous studies report prolonged auditory brainstem response (ABR) in children and adults with autism spectrum disorder (ASD). Despite its promise as a biomarker, it is unclear whether healthy newborns who later develop ASD also show ABR abnormalities. In the current study, we extracted ABR data on 139,154 newborns from their Universal Newborn Hearing Screening, including 321 newborns who were later diagnosed with ASD. We found that the ASD newborns had significant prolongations of their ABR phase and V‐negative latency compared with the non‐ASD newborns. Newborns in the ASD group also exhibited greater variance in their latencies compared to previous studies in older ASD samples, likely due in part to the low intensity of the ABR stimulus. These findings suggest that newborns display neurophysiological variation associated with ASD at birth. Future studies with higher‐intensity stimulus ABRs may allow more accurate predictions of ASD risk, which could augment the universal ABR test that currently screens millions of newborns worldwide. LAY SUMMARY: Children with autism spectrum disorder (ASD) have slow brain responses to sounds. We examined these brain responses from newborns' hearing tests and found that newborns who were later diagnosed with autism also had slower brain responses to sounds. Future studies might use these findings to better predict autism risk, with a hearing test that is already used on millions of newborns worldwide. John Wiley & Sons, Inc. 2020-11-02 2021-01 /pmc/articles/PMC7894135/ /pubmed/33140578 http://dx.doi.org/10.1002/aur.2422 Text en © 2020 The Authors. Autism Research published by International Society for Autism Research and Wiley Periodicals LLC. This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle NEUROIMAGING
Miron, Oren
Delgado, Rafael E.
Delgado, Christine F.
Simpson, Elizabeth A.
Yu, Kun‐Hsing
Gutierrez, Anibal
Zeng, Guangyu
Gerstenberger, Jillian N.
Kohane, Isaac S.
Prolonged Auditory Brainstem Response in Universal Hearing Screening of Newborns with Autism Spectrum Disorder
title Prolonged Auditory Brainstem Response in Universal Hearing Screening of Newborns with Autism Spectrum Disorder
title_full Prolonged Auditory Brainstem Response in Universal Hearing Screening of Newborns with Autism Spectrum Disorder
title_fullStr Prolonged Auditory Brainstem Response in Universal Hearing Screening of Newborns with Autism Spectrum Disorder
title_full_unstemmed Prolonged Auditory Brainstem Response in Universal Hearing Screening of Newborns with Autism Spectrum Disorder
title_short Prolonged Auditory Brainstem Response in Universal Hearing Screening of Newborns with Autism Spectrum Disorder
title_sort prolonged auditory brainstem response in universal hearing screening of newborns with autism spectrum disorder
topic NEUROIMAGING
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7894135/
https://www.ncbi.nlm.nih.gov/pubmed/33140578
http://dx.doi.org/10.1002/aur.2422
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