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感觉性颞部时间辨别阈在局灶性肌张力障碍中是否随时间变化?

Does the Somatosensory Temporal Discrimination Threshold Change over Time in Focal Dystonia?

机构信息

Department of Neurology and Psychiatry, Sapienza University Rome, Rome, Italy.

IRCCS Neuromed, Pozzilli, Italy.

出版信息

Neural Plast. 2017;2017:9848070. doi: 10.1155/2017/9848070. Epub 2017 Sep 14.

Abstract

BACKGROUND

The somatosensory temporal discrimination threshold (STDT) is defined as the shortest interval at which an individual recognizes two stimuli as asynchronous. Some evidence suggests that STDT depends on cortical inhibitory interneurons in the basal ganglia and in primary somatosensory cortex. Several studies have reported that the STDT in patients with dystonia is abnormal. No longitudinal studies have yet investigated whether STDT values in different forms of focal dystonia change during the course of the disease.

METHODS

We designed a follow-up study on 25 patients with dystonia (15 with blepharospasm and 10 with cervical dystonia) who were tested twice: upon enrolment and 8 years later. STDT values from dystonic patients at the baseline were also compared with those from a group of 30 age-matched healthy subjects.

RESULTS

Our findings show that the abnormally high STDT values observed in patients with focal dystonia remained unchanged at the 8-year follow-up assessment whereas disease severity worsened.

CONCLUSIONS

Our observation that STDT abnormalities in dystonia remain unmodified during the course of the disease suggests that the altered activity of inhibitory interneurons-either at cortical or at subcortical level-responsible for the increased STDT does not deteriorate as the disease progresses.

摘要

背景

体感时间辨别阈(STDT)定义为个体能够识别两个刺激不同时出现的最短时间间隔。一些证据表明,STDT 依赖于基底节和初级体感皮层中的皮质抑制性中间神经元。几项研究报告称,肌张力障碍患者的 STDT 异常。尚无纵向研究调查不同形式的局灶性肌张力障碍患者的 STDT 值在疾病过程中是否发生变化。

方法

我们对 25 例肌张力障碍患者(15 例眼睑痉挛和 10 例颈肌张力障碍)进行了随访研究,这些患者接受了两次测试:入组时和 8 年后。在基线时,从肌张力障碍患者中获得的 STDT 值也与 30 名年龄匹配的健康受试者的 STDT 值进行了比较。

结果

我们的研究结果表明,在 8 年的随访评估中,局灶性肌张力障碍患者异常升高的 STDT 值保持不变,而疾病严重程度恶化。

结论

我们观察到肌张力障碍患者的 STDT 异常在疾病过程中保持不变,这表明导致 STDT 升高的抑制性中间神经元的活性改变(无论是在皮质还是皮质下水平)并没有随着疾病的进展而恶化。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a901/5618781/61904ac5e033/NP2017-9848070.001.jpg

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