苍白球神经元发射率和模式的差异与肌张力障碍患儿不同的疾病生物学特性有关。

IF 2 Q3 MANAGEMENT
Equality Diversity and Inclusion Pub Date : 2016-09-01 Epub Date: 2016-02-04 DOI:10.1136/jnnp-2015-311803
V M McClelland, A Valentin, H G Rey, D E Lumsden, M C Elze, R Selway, G Alarcon, J-P Lin
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引用次数: 0

摘要

背景:不同类型肌张力障碍的病理生理学尚不清楚。我们报告了接受脑深部刺激(DBS)治疗肌张力障碍的儿童苍白球内侧(GPi)和苍白球外侧(GPe)的微电极数据,并研究了不同肌张力障碍类型的GPi和GPe发射率是否存在差异:获得了单通微电极数据,以指导 44 名患有以下肌张力障碍类型的儿童(3.3-18.1 岁,中位数 10.7 岁)的电极位置:14例原发性、22例继发性静态和8例进行性继发性神经元脑铁积聚(NBIA)。术前立体定向 MRI 确定了 GPi 目标的坐标。对数字化尖峰序列进行离线分析,对临床数据保密。术后立体定向 CT 扫描确认电极位置:我们确定了 263 个 GPi 和 87 个 GPe 细胞。GPi 和 GPe 的发射频率与肌张力障碍的病因有显著差异。原发性组 GPi 发火频率中位数高于继发性静态组(13.5 Hz vs 9.6 Hz;P=0.002),NBIA 组高于原发性组(25 Hz vs 13.5 Hz;P=0.006)或继发性静态组(25 Hz vs 9.6 Hz;P=0.00004)。NBIA 组的 GPe 发火频率中位数高于继发性静态组(15.9 Hz vs 7 Hz;p=0.013)。与其他组相比,NBIA 组也显示出更高比例的有规律发射的 GPi 细胞(p解释:苍白球的发射率和模式与肌张力障碍的病因和表型有显著差异。识别特定的发射模式有助于确定神经调控疗法的目标和针对患者的方案:国家健康研究所、盖伊和圣托马斯慈善机构、英国肌张力障碍协会、医学研究行动、德国国家学术基金会。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Differences in globus pallidus neuronal firing rates and patterns relate to different disease biology in children with dystonia.

Background: The pathophysiology underlying different types of dystonia is not yet understood. We report microelectrode data from the globus pallidus interna (GPi) and globus pallidus externa (GPe) in children undergoing deep brain stimulation (DBS) for dystonia and investigate whether GPi and GPe firing rates differ between dystonia types.

Methods: Single pass microelectrode data were obtained to guide electrode position in 44 children (3.3-18.1 years, median 10.7) with the following dystonia types: 14 primary, 22 secondary Static and 8 progressive secondary to neuronal brain iron accumulation (NBIA). Preoperative stereotactic MRI determined coordinates for the GPi target. Digitised spike trains were analysed offline, blind to clinical data. Electrode placement was confirmed by a postoperative stereotactic CT scan.

Findings: We identified 263 GPi and 87 GPe cells. Both GPi and GPe firing frequencies differed significantly with dystonia aetiology. The median GPi firing frequency was higher in the primary group than in the secondary static group (13.5 Hz vs 9.6 Hz; p=0.002) and higher in the NBIA group than in either the primary (25 Hz vs 13.5 Hz; p=0.006) or the secondary static group (25 Hz vs 9.6 Hz; p=0.00004). The median GPe firing frequency was higher in the NBIA group than in the secondary static group (15.9 Hz vs 7 Hz; p=0.013). The NBIA group also showed a higher proportion of regularly firing GPi cells compared with the other groups (p<0.001). A higher proportion of regular GPi cells was also seen in patients with fixed/tonic dystonia compared with a phasic/dynamic dystonia phenotype (p<0.001). The GPi firing frequency showed a positive correlation with 1-year outcome from DBS measured by improvement in the Burke-Fahn-Marsden Dystonia Rating Scale (BFMDRS-m) score (p=0.030). This association was stronger for the non-progressive patients (p=0.006).

Interpretation: Pallidal firing rates and patterns differ significantly with dystonia aetiology and phenotype. Identification of specific firing patterns may help determine targets and patient-specific protocols for neuromodulation therapy.

Funding: National Institute of Health Research, Guy's and St. Thomas' Charity, Dystonia Society UK, Action Medical Research, German National Academic Foundation.

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