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Sensory Alterations in Patients with Isolated Idiopathic Dystonia: An Exploratory Quantitative Sensory Testing Analysis

Abnormalities in the somatosensory system are increasingly being recognized in patients with dystonia. The aim of this study was to investigate whether sensory abnormalities are confined to the dystonic body segments or whether there is a wider involvement in patients with idiopathic dystonia. For t...

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Autores principales: Paracka, Lejla, Wegner, Florian, Blahak, Christian, Abdallat, Mahmoud, Saryyeva, Assel, Dressler, Dirk, Karst, Matthias, Krauss, Joachim K.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5650962/
https://www.ncbi.nlm.nih.gov/pubmed/29089923
http://dx.doi.org/10.3389/fneur.2017.00553
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author Paracka, Lejla
Wegner, Florian
Blahak, Christian
Abdallat, Mahmoud
Saryyeva, Assel
Dressler, Dirk
Karst, Matthias
Krauss, Joachim K.
author_facet Paracka, Lejla
Wegner, Florian
Blahak, Christian
Abdallat, Mahmoud
Saryyeva, Assel
Dressler, Dirk
Karst, Matthias
Krauss, Joachim K.
author_sort Paracka, Lejla
collection PubMed
description Abnormalities in the somatosensory system are increasingly being recognized in patients with dystonia. The aim of this study was to investigate whether sensory abnormalities are confined to the dystonic body segments or whether there is a wider involvement in patients with idiopathic dystonia. For this purpose, we recruited 20 patients, 8 had generalized, 5 had segmental dystonia with upper extremity involvement, and 7 had cervical dystonia. In total, there were 13 patients with upper extremity involvement. We used Quantitative Sensory Testing (QST) at the back of the hand in all patients and at the shoulder in patients with cervical dystonia. The main finding on the hand QST was impaired cold detection threshold (CDT), dynamic mechanical allodynia (DMA), and thermal sensory limen (TSL). The alterations were present on both hands, but more pronounced on the side more affected with dystonia. Patients with cervical dystonia showed a reduced CDT and hot detection threshold (HDT), enhanced TSL and DMA at the back of the hand, whereas the shoulder QST only revealed increased cold pain threshold and DMA. In summary, QST clearly shows distinct sensory abnormalities in patients with idiopathic dystonia, which may also manifest in body regions without evident dystonia. Further studies with larger groups of dystonia patients are needed to prove the consistency of these findings.
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spelling pubmed-56509622017-10-31 Sensory Alterations in Patients with Isolated Idiopathic Dystonia: An Exploratory Quantitative Sensory Testing Analysis Paracka, Lejla Wegner, Florian Blahak, Christian Abdallat, Mahmoud Saryyeva, Assel Dressler, Dirk Karst, Matthias Krauss, Joachim K. Front Neurol Neuroscience Abnormalities in the somatosensory system are increasingly being recognized in patients with dystonia. The aim of this study was to investigate whether sensory abnormalities are confined to the dystonic body segments or whether there is a wider involvement in patients with idiopathic dystonia. For this purpose, we recruited 20 patients, 8 had generalized, 5 had segmental dystonia with upper extremity involvement, and 7 had cervical dystonia. In total, there were 13 patients with upper extremity involvement. We used Quantitative Sensory Testing (QST) at the back of the hand in all patients and at the shoulder in patients with cervical dystonia. The main finding on the hand QST was impaired cold detection threshold (CDT), dynamic mechanical allodynia (DMA), and thermal sensory limen (TSL). The alterations were present on both hands, but more pronounced on the side more affected with dystonia. Patients with cervical dystonia showed a reduced CDT and hot detection threshold (HDT), enhanced TSL and DMA at the back of the hand, whereas the shoulder QST only revealed increased cold pain threshold and DMA. In summary, QST clearly shows distinct sensory abnormalities in patients with idiopathic dystonia, which may also manifest in body regions without evident dystonia. Further studies with larger groups of dystonia patients are needed to prove the consistency of these findings. Frontiers Media S.A. 2017-10-17 /pmc/articles/PMC5650962/ /pubmed/29089923 http://dx.doi.org/10.3389/fneur.2017.00553 Text en Copyright © 2017 Paracka, Wegner, Blahak, Abdallat, Saryyeva, Dressler, Karst and Krauss. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Neuroscience
Paracka, Lejla
Wegner, Florian
Blahak, Christian
Abdallat, Mahmoud
Saryyeva, Assel
Dressler, Dirk
Karst, Matthias
Krauss, Joachim K.
Sensory Alterations in Patients with Isolated Idiopathic Dystonia: An Exploratory Quantitative Sensory Testing Analysis
title Sensory Alterations in Patients with Isolated Idiopathic Dystonia: An Exploratory Quantitative Sensory Testing Analysis
title_full Sensory Alterations in Patients with Isolated Idiopathic Dystonia: An Exploratory Quantitative Sensory Testing Analysis
title_fullStr Sensory Alterations in Patients with Isolated Idiopathic Dystonia: An Exploratory Quantitative Sensory Testing Analysis
title_full_unstemmed Sensory Alterations in Patients with Isolated Idiopathic Dystonia: An Exploratory Quantitative Sensory Testing Analysis
title_short Sensory Alterations in Patients with Isolated Idiopathic Dystonia: An Exploratory Quantitative Sensory Testing Analysis
title_sort sensory alterations in patients with isolated idiopathic dystonia: an exploratory quantitative sensory testing analysis
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5650962/
https://www.ncbi.nlm.nih.gov/pubmed/29089923
http://dx.doi.org/10.3389/fneur.2017.00553
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