Abstract
Objective: To characterize neurophysiological subcortical abnormalities in myoclonus–dystonia and their modulation by alcohol administration. Methods: Cerebellar associative learning and basal ganglia–brainstem interaction were investigated in 17 myoclonus–dystonia patients with epsilon-sarcoglycan (SGCE) gene mutation and 21 age- and sex-matched healthy controls by means of classical eyeblink conditioning and blink reflex recovery cycle before and after alcohol intake resulting in a breath alcohol concentration of 0.08% (0.8g/l). The alcohol responsiveness of clinical symptoms was evaluated by 3 blinded raters with a standardized video protocol and clinical rating scales including the Unified Myoclonus Rating Scale and the Burke–Fahn–Marsden Dystonia Rating Scale. Results: Patients showed a significantly reduced number of conditioned eyeblink responses before alcohol administration compared to controls. Whereas the conditioning response rate decreased under alcohol intake in controls, it increased in patients (analysis of variance: alcohol state × group, p = 0.004). Blink reflex recovery cycle before and after alcohol intake did not differ between groups. Myoclonus improved significantly after alcohol intake (p = 0.016). The severity of action myoclonus at baseline correlated negatively with the conditioning response in classical eyeblink conditioning in patients. Interpretation: The combination of findings of reduced baseline acquisition of conditioned eyeblink responses and normal blink reflex recovery cycle in patients who improved significantly with alcohol intake suggests a crucial role of cerebellar networks in the generation of symptoms in these patients. Ann Neurol 2017;82:543–553.
| Original language | English |
|---|---|
| Journal | Annals of Neurology |
| Volume | 82 |
| Issue number | 4 |
| Pages (from-to) | 543-553 |
| Number of pages | 11 |
| ISSN | 0364-5134 |
| DOIs | |
| Publication status | Published - 01.10.2017 |
Funding
This work was supported by the Deutsche Forschungsge-meinschaft (DFG; SFB 936/project C5, C.K., A.M.) and German Bundesministerium fu€r Bildung und Forschung (BMBF) through a project grant (Dystonia Translational Research and Therapy Consortium [DysTract]). A.W. received a scholarship from the DFG (WE5919/1-1) and a habilitation stipend from the University of Lu€beck (H03-2016). K.E.Z. has been supported by the DFG, University of Schleswig Holstein, and Benign Essential Blepharospasmus Foundation. N.B. was funded by the Collaborative Center for X-linked Dystonia-Parkinsonism. A.L. received grants from Brain Canada, Canadian Institutes of Health Research, Edmond J. Safra Philanthropic Foundation, Michael J. Fox Foundation, Ontario Brain Institute, National Parkinson Foundation, Parkinson Society Canada, and W. Garfield Weston Foundation. C.K. is the recipient of a career development award from the Hermann and Lilly Schilling Foundation. A.M. receives support from the Possehl-Stiftung, Lu€beck; the Margot und Ju€rgen Wessel Stiftung, Lubeck; the DFG (SFB 936, project C5), and the BMBF (DysTract consortium, the Innovationsausschuss of the Gemeinsamer Bun-desausschuss: Translate NAMSE; structural support for the Lu€beck Center for Rare Diseases).
UN SDGs
This output contributes to the following UN Sustainable Development Goals (SDGs)
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SDG 3 Good Health and Well-being
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SDG 10 Reduced Inequalities
Research Areas and Centers
- Academic Focus: Center for Brain, Behavior and Metabolism (CBBM)
Fingerprint
Dive into the research topics of 'Alcohol improves cerebellar learning deficit in myoclonus–dystonia: A clinical and electrophysiological investigation'. Together they form a unique fingerprint.Projects
- 1 Finished
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Motor cortex plasticity induction by pairing subthalamic nucleus deep brain stimulation and dorsal premotor cortical transcranial magnetic stimulation in Parkinsons disease
Weißbach, A. (Principal Investigator (PI)) & Chen, R. (Project Staff)
01.01.16 → 31.12.17
Project: DFG Individual Projects › DFG Scholarships: Research Fellowships
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