4.7 Article

Multivariate classification provides a neural signature of Tourette disorder

期刊

PSYCHOLOGICAL MEDICINE
卷 53, 期 6, 页码 2361-2369

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CAMBRIDGE UNIV PRESS
DOI: 10.1017/S0033291721004232

关键词

Tourette disorder; resting state fMRI; multivariate analysis; support vector machine

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This study used a data-driven approach to investigate the functional connectivity of brain networks in patients with Tourette disorder (TD). The results showed that there are distinct differences in connectivity patterns between TD patients and controls, as well as between medicated and unmedicated TD patients. These findings hold potential for the development of imaging-based biomarkers for TD diagnosis and treatment evaluation.
Background Tourette disorder (TD), hallmarks of which are motor and vocal tics, has been related to functional abnormalities in large-scale brain networks. Using a fully data driven approach in a prospective, case-control study, we tested the hypothesis that functional connectivity of these networks carries a neural signature of TD. Our aim was to investigate (i) the brain networks that distinguish adult patients with TD from controls, and (ii) the effects of antipsychotic medication on these networks. Methods Using a multivariate analysis based on support vector machine (SVM), we developed a predictive model of resting state functional connectivity in 48 patients and 51 controls, and identified brain networks that were most affected by disease and pharmacological treatments. We also performed standard univariate analyses to identify differences in specific connections across groups. Results SVM was able to identify TD with 67% accuracy (p = 0.004), based on the connectivity in widespread networks involving the striatum, fronto-parietal cortical areas and the cerebellum. Medicated and unmedicated patients were discriminated with 69% accuracy (p = 0.019), based on the connectivity among striatum, insular and cerebellar networks. Univariate approaches revealed differences in functional connectivity within the striatum in patients v. controls, and between the caudate and insular cortex in medicated v. unmedicated TD. Conclusions SVM was able to identify a neuronal network that distinguishes patients with TD from control, as well as medicated and unmedicated patients with TD, holding a promise to identify imaging-based biomarkers of TD for clinical use and evaluation of the effects of treatment.

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