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Clinical effects of pallidal stimulation in dystonia are quantitatively related to intracortical inhibition

A. Fecíková, V. Cejka, V. Capek, F. Ruzicka, V. Bocek, D. Štastná, I. Štetkárová, D. Urgošík, R. Jech (Praha, Czech Republic)

Meeting: 2016 International Congress

Abstract Number: 1646

Keywords: Deep brain stimulation (DBS), Globus pallidus, Transcranial magnetic stimulation(TMS)

Session Information

Date: Thursday, June 23, 2016

Session Title: Dystonia

Session Time: 12:00pm-1:30pm

Location: Exhibit Hall located in Hall B, Level 2

Objective: To distinguish between patients with dystonia according to the clinical outcome of pallidal stimulation (GPi DBS) using intracortical inhibition of the motor cortex assessed by paired transcranial magnetic stimulation (TMS).

Background: GPi DBS is an effective treatment for dystonic syndromes with a relatively high variability of clinical benefit. Patients with dystonia typically have a lower ability to suppress unwanted movements. Therefore we expected a decreased intracortical inhibition of motor cortex in these patients, which can be potentially reversed by GPi DBS.

Methods: We examined 22 patients (mean age 51±(SD)17 years) with dystonia of various distribution and origin treated by GPi DBS in different time intervals from implantation

Descriptive patient’s data
Patient Age at onset Body distribution Etiology Duration of GPi DBS (years) BFMDS/TWSTRS before surgery BFMDS/TWSTRS GPi DBS ON Responsiveness
1 Late adulthood Generalized Idiopathic 4 39 28.5 Partial responder
2 Childhood Generalized DYT 1 6 27 2.5 Responder
3 Early adulthood Generalized Idiopathic 3 50 22.5 Responder
4 Childhood Generelized Postanoxic 1 47.5 46 Non-responder
5 Childhood Generelized DYT 1 5 28.5 14 Responder
6 Childhood Generelized PKAN 9 77.5 55 Partial responder
7 Childhood Generelized PKAN 8 70.5 80 Non-responder
8 Infancy Generelized Postanoxic 3 50.5 47.5 Non-responder
9 Late adulthood Generelized Idiopathic 4 15 x Non-responder
10 Late adulthood Generelized Idiopathic 3 8 0 Responder
11 Late adulthood Generelized Idiopathic 5 20.5 7 Responder
12 Early adulthood Generelized Idiopathic 6 29 24.5 Non-responder
13 Late adulthood Generelized Idiopathic 2 33 13.5 Responder
14 Late adulthood Generelized Idiopathic 3 21 12.5 Partial responder
15 Late adulthood Generelized Possible MSA-P 1 16.6 15.5 Non-responder
16 Early adulthood Cervical Idiopathic 4 24 17 Partial responder
17 Early adulthood Cervical Idiopathic 4 20 16 Non-responder
18 Late adulthood Cervical Idiopathic 1 26 22 Non-responder
19 Early adulthood Cervical Idiopathic 5 24 5 Responder
20 Late adulthood Cervical Idiopathic 3 25 22 Non-responder
21 Childhood Cervical Idiopathic 4 29 6 Responder
22 Early adulthood Cervical Idiopathic 7 24 14 Partial responder
. Paired TMS with subthreshold conditioning stimuli followed by a supratreshold testing stimuli 2.5 ms later were applied to the motor cortex to elicit short-latency intracortical inhibition (SICI) of motor evoked potentials (MEP) in the abductor pollicis brevis muscle in two conditions: (i) in GPi DBS ON and (ii) in GPi DBS OFF condition two hours later. The clinical effect (CE) was expressed as a change in the dystonic score (Burke-Fahn-Marsden Dystonia rating Scale or Toronto Western Spasmodic Torticollis Scale) between actual GPi DBS ON condition and the preoperative state.

Results: The SICI was less effective in patients than in controls regardless of the ON and OFF conditions (p<0.001). Non-responders (n=9; <25% CE) showed abnormally low SICI, partial responders (n=5; 25%-50% CE) showed higher SICI and the highest SICI was in responders (n=8; >50% CE, p<0.05). The MEP onset latency was shorter in patients in GPi DBS ON than in OFF condition (p<0.001). In addition, the shortest MEP onset latency was observed in non-responders, followed by partial responders and responders (p<0.001).

Conclusions: Our results suggest that the best responders to chronic GPi DBS treatment exhibited a similar level of intracortical inhibition as in healthy controls. On the contrary, non-responders were unable to increase their reduced cortical inhibition and effectively suppressed dystonic symptoms. We speculate that decreased intracortical inhibition with abnormally fast transmission volley in these patients is underpinned by the poor complexity of the motor network. Supported by the grant IGA MZ CR NT12282-5/2011.

To cite this abstract in AMA style:

A. Fecíková, V. Cejka, V. Capek, F. Ruzicka, V. Bocek, D. Štastná, I. Štetkárová, D. Urgošík, R. Jech. Clinical effects of pallidal stimulation in dystonia are quantitatively related to intracortical inhibition [abstract]. Mov Disord. 2016; 31 (suppl 2). https://www.mdsabstracts.org/abstract/clinical-effects-of-pallidal-stimulation-in-dystonia-are-quantitatively-related-to-intracortical-inhibition/. Accessed May 13, 2025.
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