Kimmich O1,2, Molloy A1,2, Whelan R3, Williams L1,2, Bradley D1,3, Balsters J4, Molloy F5, Lynch T6, Healy DG7, Walsh C8, O’Riordan S1,2, Reilly RB3, Hutchinson M1,2

 

Mov Disord. 2014 May;29(6):804-11. doi: 10.1002/mds.25822. Epub 2014 Jan 30.

 

Author affiliations:
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1 Department of Neurology, St. Vincent’s University Hospital, Dublin, Ireland.
2 School of Medicine and Medical Science, University College Dublin, Belfield, Dublin, Ireland.
3 Trinity Centre for Bioengineering, Trinity College Dublin, Dublin, Ireland.
4 Trinity College Institute of Neuroscience, Trinity College Dublin, Ireland.
5 Department of Neurophysiology, Beaumont Hospital, Dublin, Ireland.
6 Department of Neurology, Mater Misericordiae University Hospital, Dublin, Ireland.
7 Department of Neurology, Beaumont Hospital, Dublin, Ireland.
8 Department of Statistics, Trinity College Dublin, Dublin, Ireland.

ABSTRACT:


 

While the pathogenesis of cervical dystonia remains unknown, recent animal and clinical experimental studies have indicated its probable mechanisms. Abnormal temporal discrimination is a mediational endophenotype of cervical dystonia and informs new concepts of disease pathogenesis. Our hypothesis is that both abnormal temporal discrimination and cervical dystonia are due to a disorder of the midbrain network for covert attentional orienting caused by reduced gamma-aminobutyric acid (GABA) inhibition, resulting, in turn, from as yet undetermined, genetic mutations. Such disinhibition is (a) subclinically manifested by abnormal temporal discrimination due to prolonged duration firing of the visual sensory neurons in the superficial laminae of the superior colliculus and (b) clinically manifested by cervical dystonia due to disinhibited burst activity of the cephalomotor neurons of the intermediate and deep laminae of the superior colliculus. Abnormal temporal discrimination in unaffected first-degree relatives of patients with cervical dystonia represents a subclinical manifestation of defective GABA activity both within the superior colliculus and from the substantia nigra pars reticulata. A number of experiments are required to prove or disprove this hypothesis.

 


 

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© 2014 International Parkinson and Movement Disorder Society.