Predicting Autism Spectrum Disorder Using Blood-based Gene Expression Signatures and Machine Learning

被引:28
作者
Oh, Dong Hoon [1 ]
Kim, Il Bin [2 ]
Kim, Seok Hyeon [3 ,4 ]
Ahn, Dong Hyun [3 ,4 ]
机构
[1] Hanyang Univ, Inst Hlth & Soc, Seoul, South Korea
[2] Korea Adv Inst Sci & Technol, Grad Sch Med Sci & Engn, Translat Neurogenet Lab, Daejeon, South Korea
[3] Hanyang Univ, Coll Med, Dept Psychiat, Seoul, South Korea
[4] Hanyang Univ, Coll Med, Inst Mental Hlth, Seoul, South Korea
关键词
Autism spectrum disorder; Blood; Microarray analysis; Transcriptome; Machine learning; Decision support techniques; MITOCHONDRIAL DYSFUNCTION; ABNORMALITIES; RECURRENCE; CHILDREN; TODDLERS; SYSTEM;
D O I
10.9758/cpn.2017.15.1.47
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Objective: The aim of this study was to identify a transcriptomic signature that could be used to classify subjects with autism spectrum disorder (ASD) compared to controls on the basis of blood gene expression profiles. The gene expression profiles could ultimately be used as diagnostic biomarkers for ASD. Methods: We used the published microarray data (GSE26415) from the Gene Expression Omnibus database, which included 21 young adults with ASD and 21 age and sex matched unaffected controls. Nineteen differentially expressed probes were identified from a training dataset (n=26, 13 ASD cases and 13 controls) using the limma package in R language (adjusted p value <0.05) and were further analyzed in a test dataset (n=16, 8 ASD cases and 8 controls) using machine learning algorithms. Results: Hierarchical cluster analysis showed that subjects with ASD were relatively well discriminated from controls. Based on the support vector machine and K nearest neighbors analysis, validation of 19 DE probes with a test dataset resulted in an overall class prediction accuracy of 93.8% as well as a sensitivity and specificity of 100% and 87.5%, respectively. Conclusion: The results of our exploratory study suggest that the gene expression profiles identified from the peripheral blood samples of young adults with ASD can be used to identify a biological signature for ASD. Further study using a larger cohort and more homogeneous datasets is required to improve the diagnostic accuracy.
引用
收藏
页码:47 / 52
页数:6
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