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苍白球刺激治疗原发性全身性肌张力障碍:对认知、情绪和生活质量的影响。

Pallidal stimulation for primary generalised dystonia: effect on cognition, mood and quality of life.

机构信息

Sobell Department of Motor Neuroscience and Movement Disorders, UCL Institute of Neurology, The National Hospital for Neurology and Neurosurgery, Queen Square, London, WC1N 3BG, UK,

出版信息

J Neurol. 2014 Jan;261(1):164-73. doi: 10.1007/s00415-013-7161-2. Epub 2013 Nov 1.

Abstract

We investigated the effect of pallidal deep brain stimulation (GPi-DBS) in dystonia on cognition, mood, and quality of life and also assessed if DYT1 gene status influenced cognitive outcome following GPi-DBS. Fourteen patients with primary generalized dystonia (PGD) were assessed, measuring their estimated premorbid and current IQ, memory for words and faces, and working memory, language, executive function, and sustained attention, one month before and one year or more after surgery. Changes in mood and behaviour and quality of life were also assessed. There was a significant improvement of dystonia with GPi-DBS (69 % improvement in Burke-Fahn-Marsden score, p < 0.0001). Performance on five cognitive tests either improved or declined at post-surgical follow-up. Calculation of a reliable change index suggested that deterioration in sustained attention on the PASAT was the only reliable change (worse after surgery) in cognition with GPi-DBS. DYT1 gene status did not influence cognitive outcome following GPi-DBS. Depression, anxiety and apathy were not significantly altered, and ratings of health status on the EQ5D remained unchanged. In our sample, GPi-DBS was only associated with an isolated deficit on a test of sustained attention, confirming that GPi-DBS in PGD is clinically effective and safe, without adverse effects on the main domains of cognitive function. The dissociation between GPi-DBS improving dystonia, but not having a significant positive impact on the patients' QoL, warrants further investigation.

摘要

我们研究了苍白球深部脑刺激(GPi-DBS)对肌张力障碍患者认知、情绪和生活质量的影响,还评估了 DYT1 基因突变状态是否会影响 GPi-DBS 后的认知结果。我们评估了 14 例原发性全身性肌张力障碍(PGD)患者,测量了他们术前和术后 1 个月或更长时间的预估发病前和当前智商、词语和面孔记忆、工作记忆、语言、执行功能和持续注意力,同时还评估了情绪和行为变化以及生活质量。GPi-DBS 显著改善了肌张力障碍(Burke-Fahn-Marsden 评分改善 69%,p<0.0001)。五项认知测试中的表现要么在术后随访中得到改善,要么下降。可靠变化指数的计算表明,PASAT 上持续注意力的恶化是 GPi-DBS 后认知方面唯一可靠的变化(手术后更差)。DYT1 基因突变状态并不影响 GPi-DBS 后的认知结果。抑郁、焦虑和淡漠没有明显改变,EQ5D 上的健康状况评分也没有改变。在我们的样本中,GPi-DBS 仅与持续注意力测试中的孤立缺陷有关,这证实了 GPi-DBS 治疗 PGD 是临床有效的、安全的,不会对认知功能的主要领域产生不良影响。GPi-DBS 改善肌张力障碍,但对患者的生活质量没有显著积极影响,这一现象值得进一步研究。

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