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孤立性特发性肌张力障碍患者的感觉改变:一项探索性定量感觉测试分析

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

作者信息

Paracka Lejla, Wegner Florian, Blahak Christian, Abdallat Mahmoud, Saryyeva Assel, Dressler Dirk, Karst Matthias, Krauss Joachim K

机构信息

Department of Neurology, Hannover Medical School, Hannover, Germany.

Center for Systems Neuroscience, Hannover, Germany.

出版信息

Front Neurol. 2017 Oct 17;8:553. doi: 10.3389/fneur.2017.00553. eCollection 2017.

DOI:10.3389/fneur.2017.00553
PMID:29089923
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5650962/
Abstract

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.

摘要

肌张力障碍患者的体感系统异常越来越受到认可。本研究的目的是调查感觉异常是否仅限于肌张力障碍的身体节段,还是在特发性肌张力障碍患者中存在更广泛的受累情况。为此,我们招募了20名患者,其中8名患有全身性肌张力障碍,5名患有上肢受累的节段性肌张力障碍,7名患有颈部肌张力障碍。总共有13名患者上肢受累。我们对所有患者的手背进行了定量感觉测试(QST),对颈部肌张力障碍患者的肩部进行了测试。手部QST的主要发现是冷觉检测阈值(CDT)受损、动态机械性痛觉过敏(DMA)和热感觉阈(TSL)。双手均存在这些改变,但在肌张力障碍更严重的一侧更为明显。颈部肌张力障碍患者表现为手背的CDT和热觉检测阈值(HDT)降低,TSL和DMA增强,而肩部QST仅显示冷痛阈值和DMA增加。总之,QST清楚地显示了特发性肌张力障碍患者存在明显的感觉异常,这些异常也可能出现在没有明显肌张力障碍的身体部位。需要对更大组的肌张力障碍患者进行进一步研究,以证明这些发现的一致性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/28ec/5650962/a6dd9e1ade4f/fneur-08-00553-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/28ec/5650962/a6dd9e1ade4f/fneur-08-00553-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/28ec/5650962/a6dd9e1ade4f/fneur-08-00553-g001.jpg

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