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Early Auditory Temporal Processing Deficit in Children with Autism Spectrum Disorder: The Research Domain Criteria Framework
被引:0
|作者:
Atigh, Atoosa Sanglakh Ghoochan
[1
]
Joghataei, Mohammad Taghi
[1
]
Moradkhani, Shadi
[2
]
Zarei, Mehdi Alizadeh
[3
]
Nazari, Mohammad Ali
[1
]
机构:
[1] Iran Univ Med Sci, Fac Adv Technol Med, Dept Neurosci, Tehran 1449614535, Iran
[2] Univ Tabriz, Fac Psychol & Educ Sci, Dept Neurosci, Tabriz 5166616471, Iran
[3] Iran Univ Med Sci, Sch Rehabil Sci, Occupat Therapy Dept, Tehran 1545913487, Iran
关键词:
autism spectrum disorder (ASD);
biomarker;
electrophysiology;
time processing;
ISI deviant;
mismatch negativity (MMN);
MISMATCH-NEGATIVITY MMN;
EVENT-RELATED POTENTIALS;
NON-SPEECH SOUNDS;
INFANCY-IMPLICATIONS;
ASPERGER-SYNDROME;
PERCEPTION;
DISCRIMINATION;
SCHIZOPHRENIA;
ATTENTION;
RDOC;
D O I:
10.3390/brainsci14090896
中图分类号:
Q189 [神经科学];
学科分类号:
071006 ;
摘要:
Altered sensory processing especially in the auditory system is considered a typical observation in children with autism spectrum disorder (ASD). Auditory temporal processing is known to be impaired in ASD children. Although research suggests that auditory temporal processing abnormalities could be responsible for the core aspects of ASD, few studies have examined early time processing and their results have been conflicting. The present event-related potential (ERP) study investigated the early neural responses to duration and inter-stimulus interval (ISI) deviants in nonspeech contexts in children with ASD and a control group of typically developing (TD) children matched in terms of age and IQ. A passive auditory oddball paradigm was employed to elicit the mismatch negativity (MMN) for change detection considering both the duration and ISI-based stimulus. The MMN results showed that the ASD group had a relatively diminished amplitude and significant delayed latency in response to duration deviants. The findings are finally discussed in terms of hyper-hyposensitivity of auditory processing and the fact that the observed patterns may potentially act as risk factors for ASD development within the research domain criteria (RDoC) framework.
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