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苍白球和丘脑深部脑刺激治疗肌阵挛-肌张力障碍。

Pallidal and thalamic deep brain stimulation in myoclonus-dystonia.

机构信息

Departments of Neurology, University Medicine Berlin, Berlin, Germany.

出版信息

Mov Disord. 2010 Aug 15;25(11):1733-43. doi: 10.1002/mds.23312.

DOI:10.1002/mds.23312
PMID:20623686
Abstract

Deep brain stimulation (DBS) of the internal globus pallidus (GPi) and ventral intermediate thalamic nucleus (VIM) are established treatment options in primary dystonia and tremor syndromes and have been reported anecdotally to be efficacious in myoclonus-dystonia (MD). We investigated short- and long-term effects on motor function, cognition, affective state, and quality of life (QoL) of GPi- and VIM-DBS in MD. Ten MD-patients (nine epsilon-sarcoglycan-mutation-positive) were evaluated pre- and post-surgically following continuous bilateral GPi- and VIM-DBS at four time points: presurgical, 6, 12, and as a last follow-up at a mean of 62.3 months postsurgically, and in OFF-, GPi-, VIM-, and GPi-VIM-DBS conditions by validated motor [unified myoclonus rating scale (UMRS), TSUI Score, Burke-Fahn-Marsden dystonia rating scale (BFMDRS)], cognitive, affective, and QoL-scores. MD-symptoms significantly improved at 6 months post-surgery (UMRS: 61.5%, TSUI Score: 36.5%, BFMDRS: 47.3%). Beneficial effects were sustained at long-term evaluation post-surgery (UMRS: 65.5%, TSUI Score: 35.1%, BFMDRS: 48.2%). QoL was significantly ameliorated; affective status and cognition remained unchanged postsurgically irrespective of the stimulation conditions. No serious long-lasting stimulation-related adverse events (AEs) were observed. Both GPi- and VIM-DBS offer equally effective and safe treatment options for MD. With respect to fewer adverse, stimulation-induced events of GPi-DBS in comparison with VIM-DBS, GPi-DBS seems to be preferable. Combined GPi-VIM-DBS can be useful in cases of incapaciting myoclonus, refractory to GPi-DBS alone.

摘要

深部脑刺激(DBS)的内苍白球(GPi)和腹侧中间丘脑核(VIM)是原发性肌张力障碍和震颤综合征的既定治疗选择,并已被报道在肌阵挛-肌张力障碍(MD)中有效。我们研究了 GPi 和 VIM-DBS 在 MD 中的短期和长期对运动功能、认知、情感状态和生活质量(QoL)的影响。10 名 MD 患者(9 名 ε-肌聚糖基因突变阳性)在连续双侧 GPi 和 VIM-DBS 手术后进行评估,共 4 个时间点:术前、6 个月、12 个月和最后一次随访,平均术后 62.3 个月,在 OFF、GPi、VIM 和 GPi-VIM-DBS 条件下,采用经验证的运动[统一肌阵挛评分量表(UMRS)、TSUI 评分、伯克-法恩-马尔丹肌张力障碍评分量表(BFMDRS)]、认知、情感和 QoL 评分。手术后 6 个月 MD 症状显著改善(UMRS:61.5%,TSUI 评分:36.5%,BFMDRS:47.3%)。手术后长期评估仍保持有益效果(UMRS:65.5%,TSUI 评分:35.1%,BFMDRS:48.2%)。QoL 明显改善;手术后无论刺激条件如何,情感状态和认知都没有变化。没有观察到严重的、持久的与刺激相关的不良事件(AEs)。GPi 和 VIM-DBS 均为 MD 提供了有效且安全的治疗选择。与 VIM-DBS 相比,GPi-DBS 引起的不良反应和刺激诱导事件较少,因此 GPi-DBS 似乎更可取。对于单独 GPi-DBS 无效的致残性肌阵挛,联合 GPi-VIM-DBS 可能有用。

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