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In vivo assessment of striatal compartments in patients with idiopathic upper limb dystonia

AJM. Paulo, J. Waugh, JPQ. de Paiva, JR. Sato, DD. de Faria, V. Borges, SMA. Silva, HB. Ferraz, PMC. Aguiar (São Paulo, Brazil)

Meeting: 2023 International Congress

Abstract Number: 852

Keywords: Basal ganglia, Dystonia: Pathophysiology, Magnetic resonance imaging(MRI)

Category: Dystonia: Pathophysiology, Imaging

Objective: To access striatal matrix and striosome compartments in patients with idiopathic upper limb dystonia using diffusion tensor imaging

Background: The striatum is an essential hub in the motor system associated with dystonia and other movement disorders. The function of the striosomes and matrix in motor control is not clear. A recently developed method using diffusion tensor imaging (DTI) enables us to distinguish compartments of the striatum, namely matrixes-like and striosomes-like voxels, in vivo. Evaluating the striatum in terms of matrixes and striosomes may allow the understanding of the neurobiology of dystonia and ultimately lead to more targeted treatments.  

Method: We analyzed 3T MRI images from 26 patients with idiopathic upper limb dystonia aged 43.88 ± 11.32 years (SD; range 19–60) with a mean disease duration of 12.55 ± 10.25 years (SD; range 1–25) and healthy controls aged 39.42 ± 11.42 years (SD; range 19–58).The striatum was parcellated by targeting cortical regions that favored striosomes (pregenual anterior cingulate, posterior orbitofrontal, anterior insular cortex, and basolateral amygdala) and matrix-favoring areas (gyrus rectus, supplementary motor area, and primary sensory and motor cortex). The bilateral striatum was assessed for changes in volume and mean fractional anisotropy (FA) value.

Results: Patients show significant reductions of left Matrix-like voxels volume relative to controls (p= 0.022), with a moderate effect size (Cohen’s d = 0.640)[Figure 1]. No difference was observed in the right striatum compartments.

Conclusion: By parcellating the striatum into striosome and matrix-like voxels, we showed that patients with idiopathic dystonia have a reduced volume in matrix-like voxels in agreement with anatomopathological findings of some genetic types of dystonia. Even in non-degenerative dystonias, volume differences may reflect an imbalance between matrix and striosome signaling, ultimately favoring the direct pathway.

Figure 1

References: Waugh, J. L., Hassan, A. A., Kuster, J. K., Levenstein, J. M., Warfield, S. K., Makris, N., … & Blood, A. J. (2022). An MRI method for parcellating the human striatum into matrix and striosome compartments in vivo. Neuroimage, 246, 118714.

To cite this abstract in AMA style:

AJM. Paulo, J. Waugh, JPQ. de Paiva, JR. Sato, DD. de Faria, V. Borges, SMA. Silva, HB. Ferraz, PMC. Aguiar. In vivo assessment of striatal compartments in patients with idiopathic upper limb dystonia [abstract]. Mov Disord. 2023; 38 (suppl 1). https://www.mdsabstracts.org/abstract/in-vivo-assessment-of-striatal-compartments-in-patients-with-idiopathic-upper-limb-dystonia/. Accessed June 14, 2025.
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