Department of Neurosurgery, Beijing Tiantan Hospital, Capital Medical University, Beijing, China.
Institute of Science and Technology for Brain-Inspired Intelligence, Fudan University, Shanghai, China; Key Laboratory of Computational Neuroscience and Brain-Inspired Intelligence (Fudan University), Ministry of Education, China.
Clin Neurophysiol. 2020 Jul;131(7):1453-1461. doi: 10.1016/j.clinph.2020.03.023. Epub 2020 Apr 10.
We focused on a rare gene mutation causing dystonia in two siblings who received globus pallidus internus deep brain stimulation (GPi-DBS). The aim was to characterize the relationship between neuronal activity patterns and clinical syndromes.
Whole exome sequencing was applied to identify the TWNK (previous symbol C10orf2) mutation; Two siblings with TWNK mutation presented as generalized dystonia with rigidity and bradykinesia; four other sporadic generalized dystonia patients underwent GPi-DBS and local field potentials (LFPs) were recorded. Oscillatory activities were illustrated with power spectra and temporal dynamics measured by the Lempel-Ziv complexity (LZC).
Normalized power spectra of GPi LFPs differed between patients with TWNK mutation and dystonia over the low beta bands. Patients with TWNK mutation had higher low beta power (15-27 Hz, unpaired t-test, corrected P < 0.0022) and lower LZC (15-27 Hz, unpaired t-test, P < 0.01) than other patients with generalized dystonia. On the other hand, the TWNK mutation patients showed decreased low frequency and beta oscillation in the GPi after DBS, as well as improved movement performance.
The LFPs were different in TWNK mutation dystonia siblings than other patients with generalized dystonia, which indicate the abnormal LFPs were related to symptoms rather than specific disease. In addition, the inhibited effect on oscillations also provided a potential evidence for DBS treatment on rare movement disorders.
This study could potentially aid in the future development of adaptive DBS via rare disease LFPs comparison.
我们关注的是一种导致两名接受苍白球内侧深部脑刺激(GPi-DBS)的同胞发生肌张力障碍的罕见基因突变。目的是描述神经元活动模式与临床综合征之间的关系。
应用全外显子组测序鉴定 TWNK(先前的符号 C10orf2)突变;两名 TWNK 突变的同胞表现为伴有僵硬和运动迟缓的全身性肌张力障碍;另外 4 名散发性全身性肌张力障碍患者接受了 GPi-DBS,并记录了局部场电位(LFPs)。通过 Lempel-Ziv 复杂度(LZC)测量的功率谱和时间动态来说明振荡活动。
TWNK 突变患者与低β频段的肌张力障碍患者的 GPi LFPs 归一化功率谱不同。与其他全身性肌张力障碍患者相比,TWNK 突变患者的低β频段(15-27 Hz,未配对 t 检验,校正 P < 0.0022)的功率更高,LZC 更低(15-27 Hz,未配对 t 检验,P < 0.01)。另一方面,TWNK 突变患者在 DBS 后 GPi 中的低频和β振荡减少,运动表现改善。
TWNK 突变肌张力障碍同胞的 LFPs 与其他全身性肌张力障碍患者不同,这表明异常 LFPs 与症状有关,而不是与特定疾病有关。此外,对振荡的抑制作用也为 DBS 治疗罕见运动障碍提供了潜在的证据。
通过比较罕见疾病 LFPs,本研究有可能有助于未来开发适应性 DBS。