Neurodevelopmental Hypothesis about the Etiology of Autism Spectrum Disorders

Previous models or hypotheses of autism spectral disorder (ASD) failed to take into full consideration the chronological and causal developmental trajectory, leading to the emergence of diverse phenotypes through a complex interaction between individual etiologies and environmental factors. Those ph...

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Main Authors: Toshio Inui, Shinichiro Kumagaya, Masako Myowa-Yamakoshi
Format: Article
Language:English
Published: Frontiers Media S.A. 2017-07-01
Series:Frontiers in Human Neuroscience
Subjects:
Online Access:http://journal.frontiersin.org/article/10.3389/fnhum.2017.00354/full
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spelling doaj-dbb89d4fca5c4a24808f8a8e307915152020-11-25T02:02:59ZengFrontiers Media S.A.Frontiers in Human Neuroscience1662-51612017-07-011110.3389/fnhum.2017.00354256095Neurodevelopmental Hypothesis about the Etiology of Autism Spectrum DisordersToshio Inui0Shinichiro Kumagaya1Masako Myowa-Yamakoshi2Department of Psychology, Otemon Gakuin UniversityOsaka, JapanResearch Center for Advanced Science and Technology, The University of TokyoTokyo, JapanGraduate School of Education, Kyoto UniversityKyoto, JapanPrevious models or hypotheses of autism spectral disorder (ASD) failed to take into full consideration the chronological and causal developmental trajectory, leading to the emergence of diverse phenotypes through a complex interaction between individual etiologies and environmental factors. Those phenotypes include persistent deficits in social communication and social interaction (criteria A in DSM-5), and restricted, repetitive patterns of behavior, interests, or activities (criteria B in DSM-5). In this article, we proposed a domain-general model that can explain criteria in DSM-5 based on the assumption that the same etiological mechanism would trigger the various phenotypes observed in different individuals with ASD. In the model, we assumed the following joint causes as the etiology of autism: (1) Hypoplasia of the pons in the brainstem, occurring immediately following neural tube closure; and (2) Deficiency in the GABA (γ-aminobutyric acid) developmental switch during the perinatal period. Microstructural abnormalities of the pons directly affect both the structural and functional development of the brain areas strongly connected to it, especially amygdala. The impairment of GABA switch could not only lead to the deterioration of inhibitory processing in the neural network, but could also cause abnormal cytoarchitecture. We introduced a perspective that atypical development in both brain structure and function can give full explanation of diverse phenotypes and pathogenetic mechanism of ASD. Finally, we discussed about neural mechanisms underlying the phenotypic characteristics of ASD that are not described in DSM-5 but should be considered as important foundation: sleep, global precedence, categorical perception, intelligence, interoception and motor control.http://journal.frontiersin.org/article/10.3389/fnhum.2017.00354/fullautism spectral disorderetiologydomain-general modelponsGABA switch
collection DOAJ
language English
format Article
sources DOAJ
author Toshio Inui
Shinichiro Kumagaya
Masako Myowa-Yamakoshi
spellingShingle Toshio Inui
Shinichiro Kumagaya
Masako Myowa-Yamakoshi
Neurodevelopmental Hypothesis about the Etiology of Autism Spectrum Disorders
Frontiers in Human Neuroscience
autism spectral disorder
etiology
domain-general model
pons
GABA switch
author_facet Toshio Inui
Shinichiro Kumagaya
Masako Myowa-Yamakoshi
author_sort Toshio Inui
title Neurodevelopmental Hypothesis about the Etiology of Autism Spectrum Disorders
title_short Neurodevelopmental Hypothesis about the Etiology of Autism Spectrum Disorders
title_full Neurodevelopmental Hypothesis about the Etiology of Autism Spectrum Disorders
title_fullStr Neurodevelopmental Hypothesis about the Etiology of Autism Spectrum Disorders
title_full_unstemmed Neurodevelopmental Hypothesis about the Etiology of Autism Spectrum Disorders
title_sort neurodevelopmental hypothesis about the etiology of autism spectrum disorders
publisher Frontiers Media S.A.
series Frontiers in Human Neuroscience
issn 1662-5161
publishDate 2017-07-01
description Previous models or hypotheses of autism spectral disorder (ASD) failed to take into full consideration the chronological and causal developmental trajectory, leading to the emergence of diverse phenotypes through a complex interaction between individual etiologies and environmental factors. Those phenotypes include persistent deficits in social communication and social interaction (criteria A in DSM-5), and restricted, repetitive patterns of behavior, interests, or activities (criteria B in DSM-5). In this article, we proposed a domain-general model that can explain criteria in DSM-5 based on the assumption that the same etiological mechanism would trigger the various phenotypes observed in different individuals with ASD. In the model, we assumed the following joint causes as the etiology of autism: (1) Hypoplasia of the pons in the brainstem, occurring immediately following neural tube closure; and (2) Deficiency in the GABA (γ-aminobutyric acid) developmental switch during the perinatal period. Microstructural abnormalities of the pons directly affect both the structural and functional development of the brain areas strongly connected to it, especially amygdala. The impairment of GABA switch could not only lead to the deterioration of inhibitory processing in the neural network, but could also cause abnormal cytoarchitecture. We introduced a perspective that atypical development in both brain structure and function can give full explanation of diverse phenotypes and pathogenetic mechanism of ASD. Finally, we discussed about neural mechanisms underlying the phenotypic characteristics of ASD that are not described in DSM-5 but should be considered as important foundation: sleep, global precedence, categorical perception, intelligence, interoception and motor control.
topic autism spectral disorder
etiology
domain-general model
pons
GABA switch
url http://journal.frontiersin.org/article/10.3389/fnhum.2017.00354/full
work_keys_str_mv AT toshioinui neurodevelopmentalhypothesisabouttheetiologyofautismspectrumdisorders
AT shinichirokumagaya neurodevelopmentalhypothesisabouttheetiologyofautismspectrumdisorders
AT masakomyowayamakoshi neurodevelopmentalhypothesisabouttheetiologyofautismspectrumdisorders
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