4.4 Article

Abnormal regional homogeneity and its relationship with symptom severity in cervical dystonia: a rest state fMRI study

Journal

BMC NEUROLOGY
Volume 21, Issue 1, Pages -

Publisher

BMC
DOI: 10.1186/s12883-021-02079-x

Keywords

Cervical dystonia; Resting-state functional magnetic resonance; Regional homogeneity; Default mode network

Funding

  1. National Natural Science Foundation of China [81460203]
  2. Guangxi Appropriate Technology for Medical and Health Research and Development Project [S201415-05]

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The study revealed altered regional homogeneity (ReHo) in cervical dystonia patients, particularly in regions related to the pain matrix, salience network, motor network, and cerebellum. There was a significant positive correlation between symptom severity and ReHo value in the right cerebellum crus I in patients with cervical dystonia.
Background Although several brain networks play important roles in cervical dystonia (CD) patients, regional homogeneity (ReHo) changes in CD patients have not been clarified. We investigated to explore ReHo in CD patients at rest and analyzed its correlations with symptom severity as measured by Tsui scale. Methods A total of 19 CD patients and 21 gender-, age-, and education-matched healthy controls underwent fMRI scans at rest state. Data were analyzed by ReHo method. Results Patients showed increased ReHo in the right cerebellum crus I and decreased ReHo in the right superior medial prefrontal cortex (MPFC). Moreover, the right precentral gyrus, right insula, and bilateral middle cingulate gyrus also showed increased ReHo values. A significantly positive correlation was observed between ReHo value in the right cerebellum crus I and symptom severity (p < 0.05). Conclusions Our investigation suggested abnormal ReHo existed in brain regions of the pain matrix and salience network (the right insula and bilateral middle cingulate gyrus), the motor network (the right precentral gyrus), the cerebellum and MPFC and further highlighted the significance of these networks in the pathology of CD.

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