Functional MRI connectivity of the primary motor cortex in functional dystonia patients

Noemi Piramide1,2, Elisabetta Sarasso1, Aleksandra Tomic3

  • 1Neuroimaging Research Unit, Division of Neuroscience, IRCCS San Raffaele Scientific Institute, Via Olgettina, 60, 20132, Milan, Italy.

Journal of Neurology
|November 13, 2021
PubMed
Abstract

Insights

Functional dystonia (FD) is linked to altered brain functional connectivity (FC) in motor circuits. Fixed FD shows reduced FC in sense of agency areas, while mobile FD shows altered sensorimotor and emotional processing connectivity.

Area of Science:

  • Neuroscience
  • Neurology
  • Functional Movement Disorders

Background:

  • Functional movement disorders (FMDs) encompass a range of conditions lacking an identifiable organic cause.
  • Functional dystonia (FD) is a subtype of FMD characterized by involuntary muscle contractions.

Purpose of the Study:

  • To investigate functional connectivity (FC) alterations in the primary motor (M1) cortex in patients with functional dystonia (FD).
  • To compare FC patterns between different clinical phenotypes of FD (fixed vs. mobile) and healthy controls.

Main Methods:

  • Resting-state functional magnetic resonance imaging (fMRI) was used in 40 FD patients and 43 healthy controls.
  • Seed-based FC analysis focused on bilateral M1 regions of interest.
  • Participants included fixed FD (FixFD), mobile FD (MobFD), young healthy controls (yHC), and older healthy controls (oHC).

Main Results:

  • FD patients exhibited reduced FC between M1 and areas like the dorsal anterior cingulate cortex, SMA, PCC, and precuneus compared to controls.
  • FixFD patients showed reduced M1-precuneus FC relative to yHC.
  • MobFD patients displayed altered FC in sensorimotor and visual areas, with both reduced and increased connectivity patterns compared to oHC.

Conclusions:

  • Altered brain functional connectivity in motor circuits, involving emotional processing and sense of agency networks, is implicated in FD.
  • Distinct FC abnormalities were observed between fixed and mobile FD phenotypes, suggesting different underlying neural mechanisms.