Multivariate techniques enable a biochemical classification of children with autism spectrum disorder versus typically-developing peers: A comparison and validation study
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Final Published version
Author
Howsmon, Daniel PVargason, Troy
Rubin, Robert A
Delhey, Leanna
Tippett, Marie
Rose, Shannon
Bennuri, Sirish C
Slattery, John C
Melnyk, Stepan
James, S Jill
Frye, Richard E
Hahn, Juergen
Affiliation
Univ Arizona, Coll MedIssue Date
2018-05-01
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WILEYCitation
Howsmon, D. P., Vargason, T. , Rubin, R. A., Delhey, L. , Tippett, M. , Rose, S. , Bennuri, S. C., Slattery, J. C., Melnyk, S. , James, S. J., Frye, R. E. and Hahn, J. (2018), Multivariate techniques enable a biochemical classification of children with autism spectrum disorder versus typically‐developing peers: A comparison and validation study. Bioengineering & Translational Medicine, 3: 156-165. doi:10.1002/btm2.10095Rights
© 2018 The Authors. Bioengineering & Translational Medicine is published by Wiley Periodicals, Inc. on behalf of The American Institute of Chemical Engineers.Collection Information
This item from the UA Faculty Publications collection is made available by the University of Arizona with support from the University of Arizona Libraries. If you have questions, please contact us at repository@u.library.arizona.edu.Abstract
Autism spectrum disorder (ASD) is a developmental disorder which is currently only diagnosed through behavioral testing. Impaired folate-dependent one carbon metabolism (FOCM) and transsulfuration (TS) pathways have been implicated in ASD, and recently a study involving multivariate analysis based upon Fisher Discriminant Analysis returned very promising results for predicting an ASD diagnosis. This article takes another step toward the goal of developing a biochemical diagnostic for ASD by comparing five classification algorithms on existing data of FOCM/TS metabolites, and also validating the classification results with new data from an ASD cohort. The comparison results indicate a high sensitivity and specificity for the original data set and up to a 88% correct classification of the ASD cohort at an expected 5% misclassification rate for typically-developing controls. These results form the foundation for the development of a biochemical test for ASD which promises to aid diagnosis of ASD and provide biochemical understanding of the disease, applicable to at least a subset of the ASD population.Note
Open access journalISSN
2380-6761PubMed ID
30065970Version
Final published versionSponsors
National Institutes of Health [1R01AI110642]Additional Links
https://aiche.onlinelibrary.wiley.com/doi/10.1002/btm2.10095ae974a485f413a2113503eed53cd6c53
10.1002/btm2.10095
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