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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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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