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

机译:孤立性特发性肌张力障碍患者的感觉改变:探索性定量感觉测试分析。

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摘要

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.
机译:肌张力障碍患者越来越多地意识到体感系统的异常。这项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或特发性肌张力障碍患者的受累范围是否更大。为此,我们招募了20例患者,其中8例为全身性,5例为具有上肢受累的节段性肌张力障碍,7例为子宫颈肌张力障碍。共有13例上肢受累。我们在所有患者的手背和宫颈肌张力障碍患者的肩部均使用了定量感官测试(QST)。手上QST的主要发现是冷检测阈值(CDT)受损,动态机械异常性疼痛(DMA)和热感止痛(TSL)。两只手都有这种变化,但在肌张力障碍影响更大的一侧则更为明显。宫颈肌张力障碍患者的CDT和热检测阈值(HDT)降低,手背的TSL和DMA升高,而肩部QST仅显示冷痛阈值和DMA升高。总之,QST清楚地显示了特发性肌张力障碍患者的明显感觉异常,这也可能在身体区域出现,而没有明显的肌张力障碍。需要对大量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。

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