Abstract

Autism spectrum disorder (ASD) is a neurological and developmental disorder that begins early in childhood and lasts throughout a person’s life. Autism is influenced by both genetic and environmental factors. Lack of social interaction, communication problems, and a limited range of behaviors and interests are possible characteristics of autism in children, alongside other symptoms. Electroencephalograms provide useful information about changes in brain activity and hence are efficaciously used for diagnosis of neurological disease. Eighteen nonlinear features were extracted from EEG signals of 40 children with a diagnosis of autism spectrum disorder and 37 children with no diagnosis of neuro developmental disorder children. Feature selection was performed using Student’s t test, and Marginal Fisher Analysis was employed for data reduction. The features were ranked according to Student’s t test. The three most significant features were used to develop the autism index, while the ranked feature set was input to SVM polynomials 1, 2, and 3 for classification. The SVM polynomial 2 yielded the highest classification accuracy of 98.70% with 20 features. The developed classification system is likely to aid healthcare professionals as a diagnostic tool to detect autism. With more data, in our future work, we intend to employ deep learning models and to explore a cloud-based detection system for the detection of autism. Our study is novel, as we have analyzed all nonlinear features, and we are one of the first groups to have uniquely developed an autism (ASD) index using the extracted features.

Highlights

  • Autism spectrum disorder (ASD), commonly known as autism, is a complex neurological condition

  • Since the Support Vector Machine (SVM) polynomial 2 classifier was trained and tested with 20 features, it yielded a higher accuracy compared to SVM polynomials 1 and 2

  • It is noticeable that the two classes, normal and autism, are separated, and the features correlate with the classification

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Summary

Introduction

Autism spectrum disorder (ASD), commonly known as autism, is a complex neurological condition. ASD is characterized by a shortfall in social behaviors and nonverbal communications, such as avoiding eye contact or facing difficulties with controlling emotions and understanding others’ emotions, in the first three years of human life [1]. Nonspecific symptoms such as abnormal sensory perception skills and experiences, inept motor skills, and insomnia are common in some children with ASD. ASD is known to be multifactorial, stemming from both genetic and environmental influences [2]. Gene and chromosomal defects exist in approximately 10% to 20% of individuals with ASD [3], with siblings born into ASD families having a 50 times larger risk of ASD, amid a relapse rate of 5%–8% [4]

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