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Identifying motor functional neurological disorder using resting-state functional connectivity. | LitMetric

Identifying motor functional neurological disorder using resting-state functional connectivity.

Neuroimage Clin

Department of Clinical Neuroscience, Geneva University Hospital, Rue Gabrielle-Perret-Gentil 4, 1211 Geneva, Switzerland; Department of Neuroscience, University of Geneva, Campus Biotech, Chemin des Mines 9, 1202 Geneva, Switzerland; Neurology University Clinic, InselSpital, Department of Clinical Neuroscience, 3010 Bern, Switzerland. Electronic address:

Published: June 2018

Background: Motor functional neurological disorder (mFND) is a clinical diagnosis with reliable features; however, patients are reluctant to accept the diagnosis and physicians themselves bear doubts on potential misdiagnoses. The identification of a positive biomarker could help limiting unnecessary costs of multiple referrals and investigations, thus promoting early diagnosis and allowing early engagement in appropriate therapy.

Objectives: To test whether resting-state (RS) functional magnetic resonance imaging could discriminate patients suffering from mFND from healthy controls.

Methods: We classified 23 mFND patients and 25 age- and gender-matched healthy controls based on whole-brain RS functional connectivity (FC) data, using a support vector machine classifier and the standard Automated Anatomic Labeling (AAL) atlas, as well as two additional atlases for validation.

Results: Accuracy, specificity and sensitivity were over 68% (p = 0.004) to discriminate between mFND patients and controls, with consistent findings between the three tested atlases. The most discriminative connections comprised the right caudate, amygdala, prefrontal and sensorimotor regions. Post-hoc seed connectivity analyses showed that these regions were hyperconnected in patients compared to controls.

Conclusions: The good accuracy to discriminate patients from controls suggests that RS FC could be used as a biomarker with high diagnostic value in future clinical practice to identify mFND patients at the individual level.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5651543PMC
http://dx.doi.org/10.1016/j.nicl.2017.10.012DOI Listing

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