4.7 Article

Alcohol improves cerebellar learning deficit in myoclonus-dystonia: A clinical and electrophysiological investigation

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ANNALS OF NEUROLOGY
卷 82, 期 4, 页码 543-553

出版社

WILEY
DOI: 10.1002/ana.25035

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资金

  1. Deutsche Forschungsgemeinschaft (DFG) [SFB 936]
  2. German Bundesministerium fur Bildung und Forschung (BMBF)
  3. DFG [SFB 936, WE5919/1-1]
  4. University of Lubeck [H03-2016]
  5. DFG
  6. University of Schleswig Holstein
  7. Benign Essential Blepharospasmus Foundation
  8. Collaborative Center for X-linked Dystonia-Parkinsonism
  9. Brain Canada
  10. Canadian Institutes of Health Research
  11. Edmond J. Safra Philanthropic Foundation
  12. Michael J. Fox Foundation
  13. Ontario Brain Institute
  14. National Parkinson Foundation
  15. Parkinson Society Canada
  16. W. Garfield Weston Foundation
  17. Hermann and Lilly Schilling Foundation
  18. Possehl-Stiftung, Lubeck
  19. Margot und Jurgen Wessel Stiftung, Lubeck
  20. BMBF (DysTract consortium, the Innovationsausschuss of the Gemeinsamer Bundesausschuss: Translate NAMSE)

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ObjectiveTo characterize neurophysiological subcortical abnormalities in myoclonus-dystonia and their modulation by alcohol administration. MethodsCerebellar 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. ResultsPatients 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 statexgroup, 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. InterpretationThe 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

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