4.5 Article

Identifying motor functional neurological disorder using resting-state functional connectivity

期刊

NEUROIMAGE-CLINICAL
卷 17, 期 -, 页码 163-168

出版社

ELSEVIER SCI LTD
DOI: 10.1016/j.nicl.2017.10.012

关键词

Resting state functional magnetic resonance imaging; Functional connectivity; Functional neurological disorder; Biomarker; Classification

资金

  1. Swiss National Research Foundation [PZ00P3_147997]
  2. Leenards Nested Project grant
  3. Swiss National Science Foundation (SNF) [PZ00P3_147997] Funding Source: Swiss National Science Foundation (SNF)

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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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