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Brainstem Reflexes in Idiopathic Cervical Dystonia: Does Medullary Dysfunction Play a Role?

BACKGROUND: Neurophysiological markers in dystonia have so far not been sistematically applied in clinical practice due to limited reproducibility of results and low correlations with clinical findings. Exceptions might be represented by the blink reflex (BR), including its recovery cycle (BRRC) and...

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Autores principales: Manzo, Nicoletta, Tocco, Pierluigi, Ginatempo, Francesca, Bertolasi, Laura, Rocchi, Lorenzo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons, Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8015899/
https://www.ncbi.nlm.nih.gov/pubmed/33816666
http://dx.doi.org/10.1002/mdc3.13149
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author Manzo, Nicoletta
Tocco, Pierluigi
Ginatempo, Francesca
Bertolasi, Laura
Rocchi, Lorenzo
author_facet Manzo, Nicoletta
Tocco, Pierluigi
Ginatempo, Francesca
Bertolasi, Laura
Rocchi, Lorenzo
author_sort Manzo, Nicoletta
collection PubMed
description BACKGROUND: Neurophysiological markers in dystonia have so far not been sistematically applied in clinical practice due to limited reproducibility of results and low correlations with clinical findings. Exceptions might be represented by the blink reflex (BR), including its recovery cycle (BRRC) and the trigemino‐cervical reflex (TCR) which, compared to other neurophysiological methods, have shown more consistent alterations in cervical dystonia (CD). However, a comparison between the two techniques, and their possible correlation with disease symptoms, have not been thoroughly investigated. OBJECTIVES: To assess the role of BR, BRCC and TCR in the pathophysiology of idiopathic cervical dystonia. METHODS: Fourteen patients and 14 age‐matched healthy controls (HC) were recruited. Neurophysiological outcome measures included latency of R1 and R2 components of the BR, R2 amplitude, BRRC, latency and amplitude of P19/N31 complex of TCR. Clinical and demographic features of patients were also collected, including age at disease onset, disease duration, presence of tremor, sensory trick and pain. The Toronto Western Spasmodic Torticollis Rating Scale was used to characterize dystonia. RESULTS: Compared to HC, CD patients showed increased latency of the BR R2 and decreased suppression of the BRRC. They also showed increased latency of the P19 and decreased amplitude of P19/N31 complex of TCR. The latency of P19 component of TCR was positively correlated with disease duration. CONCLUSIONS: We propose that the increased latency of R2 and P19 observed here might be reflective of brainstem dysfunction, mediated either by local interneuronal excitability changes or by subtle structural damage.
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spelling pubmed-80158992021-04-02 Brainstem Reflexes in Idiopathic Cervical Dystonia: Does Medullary Dysfunction Play a Role? Manzo, Nicoletta Tocco, Pierluigi Ginatempo, Francesca Bertolasi, Laura Rocchi, Lorenzo Mov Disord Clin Pract Research Articles BACKGROUND: Neurophysiological markers in dystonia have so far not been sistematically applied in clinical practice due to limited reproducibility of results and low correlations with clinical findings. Exceptions might be represented by the blink reflex (BR), including its recovery cycle (BRRC) and the trigemino‐cervical reflex (TCR) which, compared to other neurophysiological methods, have shown more consistent alterations in cervical dystonia (CD). However, a comparison between the two techniques, and their possible correlation with disease symptoms, have not been thoroughly investigated. OBJECTIVES: To assess the role of BR, BRCC and TCR in the pathophysiology of idiopathic cervical dystonia. METHODS: Fourteen patients and 14 age‐matched healthy controls (HC) were recruited. Neurophysiological outcome measures included latency of R1 and R2 components of the BR, R2 amplitude, BRRC, latency and amplitude of P19/N31 complex of TCR. Clinical and demographic features of patients were also collected, including age at disease onset, disease duration, presence of tremor, sensory trick and pain. The Toronto Western Spasmodic Torticollis Rating Scale was used to characterize dystonia. RESULTS: Compared to HC, CD patients showed increased latency of the BR R2 and decreased suppression of the BRRC. They also showed increased latency of the P19 and decreased amplitude of P19/N31 complex of TCR. The latency of P19 component of TCR was positively correlated with disease duration. CONCLUSIONS: We propose that the increased latency of R2 and P19 observed here might be reflective of brainstem dysfunction, mediated either by local interneuronal excitability changes or by subtle structural damage. John Wiley & Sons, Inc. 2021-02-12 /pmc/articles/PMC8015899/ /pubmed/33816666 http://dx.doi.org/10.1002/mdc3.13149 Text en © 2021 The Authors. Movement Disorders Clinical Practice published by Wiley Periodicals LLC. on behalf of International Parkinson and Movement Disorder Society. This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.
spellingShingle Research Articles
Manzo, Nicoletta
Tocco, Pierluigi
Ginatempo, Francesca
Bertolasi, Laura
Rocchi, Lorenzo
Brainstem Reflexes in Idiopathic Cervical Dystonia: Does Medullary Dysfunction Play a Role?
title Brainstem Reflexes in Idiopathic Cervical Dystonia: Does Medullary Dysfunction Play a Role?
title_full Brainstem Reflexes in Idiopathic Cervical Dystonia: Does Medullary Dysfunction Play a Role?
title_fullStr Brainstem Reflexes in Idiopathic Cervical Dystonia: Does Medullary Dysfunction Play a Role?
title_full_unstemmed Brainstem Reflexes in Idiopathic Cervical Dystonia: Does Medullary Dysfunction Play a Role?
title_short Brainstem Reflexes in Idiopathic Cervical Dystonia: Does Medullary Dysfunction Play a Role?
title_sort brainstem reflexes in idiopathic cervical dystonia: does medullary dysfunction play a role?
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8015899/
https://www.ncbi.nlm.nih.gov/pubmed/33816666
http://dx.doi.org/10.1002/mdc3.13149
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