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Loss of inhibition in sensorimotor networks in focal hand dystonia
Cecile Gallea1, Priyantha Herath2, Valerie Voon3
1Human Motor Control Section, NINDS, NIH, Bethesda, MD, United States; Institut du Cerveau et de la Moelle (ICM-CRICM), Centre de Neuroimagerie de Recherche (UPMC/INSERM, UMR_975, CNRS 7225), Hôpital de la Pitié Salpétrière, Paris, France.
Objective:
To investigate GABA-ergic receptor density and associated brain functional and grey matter changes in focal hand dystonia (FHD).
Methods:
18 patients with FHD of the right hand and 18 age and gender matched healthy volunteers (HV) participated in this study. We measured the density of GABA-A receptors using [11C] Flumazenil and perfusion using [15O] H2O. Anatomical images were also used to measure grey matter volume with voxel-based morphometry (VBM).
Results:
In FHD patients compared to HV, the vermis VI of the right cerebellum and the left sensorimotor cortex had a decrease of Flumazenil binding potential (FMZ-BP), whereas the striatum and the lateral cerebellum did not show significant change. Bilateral inferior prefrontal cortex had increased FMZ-BP and an increase of perfusion, which correlated negatively with disease duration. Only the left sensorimotor cortex showed a decrease of grey matter volume.
Interpretation:
Impairments of GABAergic neurotransmission in the cerebellum and the sensorimotor cortical areas could explain different aspects of loss of inhibitory control in FHD, the former being involved in maladaptive plasticity, the latter in surround inhibition. Reorganization of the inferior prefrontal cortices, part of the associative network, might be compensatory for the loss of inhibitory control in sensorimotor circuits. These findings suggest that cerebellar and cerebral GABAergic abnormalities could play a role in the functional imbalance of striato-cerebello-cortical loops in dystonia.
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