Abstract

Tourette syndrome (TS) is a developmental neuropsychiatric disorder characterized by motor and vocal tics. Individuals with TS would benefit greatly from advances in prediction of symptom timecourse and treatment effectiveness. As a first step, we applied a multivariate method – support vector machine (SVM) classification – to test whether patterns in brain network activity, measured with resting state functional connectivity (RSFC) MRI, could predict diagnostic group membership for individuals. RSFC data from 42 children with TS (8–15 yrs) and 42 unaffected controls (age, IQ, in‐scanner movement matched) were included. While univariate tests identified no significant group differences, SVM classified group membership with ~70% accuracy (p < .001). We also report a novel adaptation of SVM binary classification that, in addition to an overall accuracy rate for the SVM, provides a confidence measure for the accurate classification of each individual. Our results support the contention that multivariate methods can better capture the complexity of some brain disorders, and hold promise for predicting prognosis and treatment outcome for individuals with TS.

Highlights

  • Tourette syndrome (TS) is a neuropsychiatric disorder with childhood onset, characterized by motor and vocal tics (Leckman, King & Bloch, 2014)

  • We found no difference in symptom severity (YGTSS Total Tic score) between the 42 children included in the final sample (M = 16.5, SD = 8.6, range 0–39) and the 41 children excluded due to motion (M = 17.2, SD = 8, range = 0–34), t(79) = 0.38, p =

  • The results of the present study demonstrate, as a first test case, that resting state functional connectivity (RSFC) data contain information for discriminating children with and without TS

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Summary

Introduction

Tourette syndrome (TS) is a neuropsychiatric disorder with childhood onset, characterized by motor and vocal tics (Leckman, King & Bloch, 2014). Tic symptoms begin at about 6–7 years of age, peak in severity in early adolescence, and improve into late adolescence and early adulthood (Leckman, Bloch, King & Scahill, 2006; Leckman, Riddle, Hardin, Ort, Swartz et al, 1998). While tics are the defining symptom of TS, the condition involves multiple neuropsychiatric problems, all of which can impact quality of life (Cavanna, Schrag, Morley, Orth, Robertson et al, 2008; Eddy, Rizzo, Gulisano, Agodi, Barchitta et al, 2011; Stewart, Greene, Lessov-Schlaggar, Church & Schlaggar, 2015)

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