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Correlated activity in globus pallidus and thalamus during voluntary reaching movement in three children with primary dystonia 3例原发性肌张力障碍患儿自主伸手运动中苍白球和丘脑的相关活动
Pub Date : 2023-02-23 DOI: 10.3389/dyst.2023.11117
M. Kasiri, Sina Javadzadeh, Jaya Nataraj, Seyyed Alireza Seyyed Mousavi, T. Sanger
Classical models of the physiology of dystonia suggest that involuntary muscle contractions are caused by inappropriately low activity in Globus Pallidus internus (GPi) that fails to adequately inhibit thalamic inputs to cortex. We test this prediction in three children with primary dystonia undergoing depth electrode recording in basal ganglia and thalamus during selection of targets for deep brain stimulation (DBS) implantation. We compare muscle activity to the power in the spectrogram of the local field potential, as well as to counts of identified spikes in GPi, subthalamic nucleus (STN), and the Ventral oralis (VoaVop) and Ventral Anterior (VA) subnuclei of the thalamus, while subjects are at rest or attempting to make active voluntary arm or leg reaching movements. In all three subjects, both spectrogram power and spike activity in GPi, STN, VoaVop, and VA are significantly positively correlated with movement. In particular, GPi and STN both increase activity during attempted movement. These results contradict the classical rate model of the physiology of dystonia, and support more recent models that propose abnormalities in the detailed pattern of activity rather than the overall lumped activity of pallidum and thalamus.
肌张力障碍生理学的经典模型表明,不自主的肌肉收缩是由内侧球(GPi)不适当的低活动引起的,GPi未能充分抑制丘脑对皮层的输入。我们在三名原发性肌张力障碍儿童中测试了这一预测,他们在选择脑深部刺激(DBS)植入靶点时,在基底节和丘脑进行深度电极记录。我们将肌肉活动与局部场电位谱图中的功率进行比较,并与GPi、丘脑底核(STN)、丘脑腹口(VoaVop)和腹前(VA)亚核中已识别的尖峰计数进行比较,同时受试者处于休息状态或试图进行主动的手臂或腿部伸展运动。在所有三个受试者中,GPi、STN、VoaVop和VA的频谱图功率和尖峰活动都与运动显著正相关。特别是,GPi和STN在尝试运动时都会增加活动。这些结果与肌张力障碍生理学的经典速率模型相矛盾,并支持最近的模型,这些模型提出了苍白球和丘脑的详细活动模式异常,而不是总体集中活动。
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引用次数: 3
DYT-TOR1A genotype alters extracellular vesicle composition in murine cell model and shows potential for biomarker discovery DYT-TOR1A基因型改变小鼠细胞模型的细胞外囊泡组成,显示出发现生物标志物的潜力
Pub Date : 2023-02-16 DOI: 10.3389/dyst.2023.11053
Connor S. King, Z. Caffall, E. Soderblom, N. Calakos
Introduction: Biomarkers that can be used to identify patient subgroups with shared pathophysiology and/or that can be used as pharmacodynamic readouts of disease state are valuable assets for successful clinical trial design. In translational research for brain diseases, extracellular vesicles (EVs) have become a high-priority target for biomarker discovery because of their ubiquity in peripheral biofluids and potential to indicate brain state. Materials and methods: Here, we applied unbiased quantitative proteomics of EVs isolated from DYT-TOR1A knockin mouse embryonic fibroblasts and littermate controls to discover candidates for protein biomarkers. We further examined the response of genotype perturbations to drug treatment conditions to determine their pharmacodynamic properties. Results: We found that many DYT-TOR1A MEF EV differences were significantly corrected by ritonavir, a drug recently shown to correct DYT-TOR1A phenotypes in cell and mouse disease models. We also used tool compounds to explore the effect of the integrated stress response (ISR), which regulates protein synthesis and is implicated in dystonia pathogenesis. Integrated stress response inhibition in WT cells partially phenocopied the effects of DYT-TOR1A on EV proteome composition, and ISR potentiation in DYT-TOR1A caused changes that paralleled ritonavir treatment. Conclusion: These results collectively show that DYT-TOR1A genotype alters EV protein composition, and these changes can be dynamically modulated by a candidate therapeutic drug and ISR activity state. These mouse model findings provide proof-of-concept that EVs may be a useful source of biomarkers in human populations and further suggest specific homologs to evaluate in cross-species validation.
引言:可用于识别具有共同病理生理学的患者亚组和/或可用作疾病状态的药效学读数的生物标志物是成功临床试验设计的宝贵资产。在脑疾病的转化研究中,细胞外小泡(EV)已成为生物标志物发现的高度优先目标,因为它们在外周生物流体中无处不在,并有可能指示大脑状态。材料和方法:在这里,我们应用从敲除DYT-TOR1A的小鼠胚胎成纤维细胞和同窝对照中分离的EVs的无偏定量蛋白质组学来发现蛋白质生物标志物的候选者。我们进一步研究了基因型扰动对药物治疗条件的反应,以确定其药效学特性。结果:我们发现,利托那韦显著纠正了许多DYT-TOR1A MEF-EV差异,利托纳韦是一种最近在细胞和小鼠疾病模型中被证明可以纠正DYT-TOR1A表型的药物。我们还使用工具化合物来探索整合应激反应(ISR)的作用,该反应调节蛋白质合成并与肌张力障碍的发病机制有关。WT细胞中的综合应激反应抑制部分表型复制了DYT-TOR1A对EV蛋白质组组成的影响,并且DYT-TOR1A中的ISR增强引起了与利托那韦处理平行的变化。结论:这些结果共同表明,DYT-TOR1A基因型改变了EV蛋白的组成,这些变化可以由候选治疗药物和ISR活性状态动态调节。这些小鼠模型的发现证明了EVs可能是人类群体中生物标志物的有用来源,并进一步提出了在跨物种验证中评估的特定同源物。
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引用次数: 0
Treatment of writer’s cramp based on current pathophysiological concepts 基于当前病理生理学概念的作家痉挛的治疗
Pub Date : 2023-02-09 DOI: 10.3389/dyst.2023.11067
K. Zeuner, A. Baumann, K. Witt
Task specific dystonia belongs to the group of focal dystonias. They are debilitating movement disorders that present with co-contraction of antagonist muscles during a specific task. The most common one is writer’s cramp. Botulinum toxin is the symptomatic standard treatment. Its response rate is 50% after 1 year, and the overall efficacy limited due to unwanted weakness in not injected muscles. The pathophysiology of writer’s cramp remains unclear, but genetic and additional environmental causes have been proposed. A possible underlying mechanism may be maladaptive reorganization in the sensorimotor cortex. Based on this background alternative treatment strategies were developed such as several different sensory and motor training programs that have been applied to reverse these brain abnormalities. In some studies, sensory and motor training were combined and adjunct with fitness exercises. They were conducted either as an outpatient setting or were established home based. Clinical outcome was measured with different clinical scales such as the writer’s cramp rating scale, the arm dystonia rating scale or the Burke, Fahn Marsden Scale. For objective assessment, kinematic handwriting parameters were analyzed. Functional or structural changes of the sensorimotor cortex were estimated using functional magnetic tomography, magnetencephalography and voxel-based morphometry. The results of these training programs were promising; however, one drawback is that the number of patients studied were small and the programs were not controlled since it is difficult to establish a control training to conduct a randomized controlled study.
特异性肌张力障碍属于局灶性肌张力障碍。它们是一种使人衰弱的运动障碍,在特定任务中表现为拮抗肌的共同收缩。最常见的是作家抽筋。肉毒杆菌毒素是标准的对症治疗方法。1年后,其反应率为50%,由于未注射肌肉出现不必要的无力,总体疗效有限。作家痉挛的病理生理学尚不清楚,但已经提出了遗传和其他环境原因。一种可能的潜在机制可能是感觉运动皮层的适应不良重组。基于这一背景,开发了替代治疗策略,例如几种不同的感觉和运动训练计划,这些计划已被应用于逆转这些大脑异常。在一些研究中,感觉和运动训练与健身运动相结合。他们要么在门诊进行,要么在家中进行。临床结果采用不同的临床量表进行测量,如作者的痉挛评定量表、手臂肌张力障碍评定量表或Burke,Fahn Marsden量表。为了客观评估,对运动学笔迹参数进行了分析。使用功能性磁断层扫描、脑磁图和基于体素的形态计量学来估计感觉运动皮层的功能或结构变化。这些培训方案的结果是有希望的;然而,一个缺点是,研究的患者数量很少,而且由于很难建立控制训练来进行随机对照研究,因此项目没有得到控制。
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引用次数: 0
Treatment of tardive dystonia: A review 迟发性肌张力障碍的治疗:综述
Pub Date : 2023-02-06 DOI: 10.3389/dyst.2023.10957
Paola Testini, S. Factor
Tardive dystonia (TD), the second most common but most disabling form of tardive syndrome, was initially described in 1982. It is caused by exposure to dopamine receptor blocking agents including antipsychotics and antiemetics. It most commonly presents as cranial or cervical dystonia. Characteristics suggestive of a TD diagnosis include a young age of onset, male predominance, and the higher prevalence of phasic cervical dystonia and retrocollis. Treatment of TD is limited. In this paper we review the literature on treatment options for TD as well as discussing a strategic approach. Options include use of clozapine which appears to have anti-dystonia properties. Other medications reported on with limited evidence include VMAT2 inhibitors, anticholinergics, clonazepam, and baclofen. Botulinum toxin has been shown to provide relief in TD in a manner similar to primary dystonia. The largest literature is on the use of deep brain stimulation (DBS) of the globus pallidus pars interna which includes blinded studies. We finish with providing an algorithm based on current knowledge.
迟发性肌张力障碍(TD)是第二常见但最致残的迟发性综合征,最初于1982年被描述。它是由接触多巴胺受体阻断剂引起的,包括抗精神病药和止吐药。它最常见的表现为颅骨或颈部肌张力障碍。提示TD诊断的特征包括发病年龄小,男性占主导地位,以及阶段性颈部肌张力障碍和后颈的患病率较高。TD的治疗是有限的。在本文中,我们回顾了有关TD治疗方案的文献,并讨论了一种战略方法。选项包括使用氯氮平,它似乎具有抗肌张力障碍的特性。据报道,其他证据有限的药物包括VMAT2抑制剂、抗胆碱能药物、氯硝西泮和巴氯芬。肉毒毒素已被证明以类似于原发性肌张力障碍的方式提供TD的缓解。最大的文献是关于苍白球内部部脑深部刺激(DBS)的使用,其中包括盲法研究。最后,我们提供了一个基于当前知识的算法。
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引用次数: 1
Transient dystonia correlates with parkinsonism after 1-methyl-4-phenyl-1,2,3,6- tetrahydropyridine in nonhuman primates. 非人类灵长类动物服用1-甲基-4-苯基-1,2,3,6-四氢吡啶后,短暂性肌张力障碍与帕金森病相关。
Pub Date : 2023-01-01 Epub Date: 2023-02-01 DOI: 10.3389/dyst.2023.11019
S A Norris, L Tian, E L Williams, J S Perlmutter

Unilateral internal carotid artery 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP) infusion in non-human primates produces transient contralateral hemi-dystonia followed by stable contralateral hemi-parkinsonism; the relationship between dystonia and parkinsonism remains unclear. We hypothesized that transient dystonia severity following MPTP correlates with parkinsonism severity. In male Macaca nemestrina (n = 3) and M. fascicularis (n = 17) we administered unilateral intra-carotid MPTP, then correlated validated blinded ratings of transient peak dystonia and delayed parkinsonism. We also correlated dystonia severity with post-mortem measures of residual striatal dopamine and nigral neuron counts obtained a mean 53 ± 15 days following MPTP, after resolution of dystonia but during stable parkinsonism. Median latency to dystonia onset was 1 day, and peak severity 2.5 days after MPTP; total dystonia duration was 13.5 days. Parkinsonism peaked a median of 19.5 days after MPTP, remaining nearly constant thereafter. Peak dystonia severity highly correlated with parkinsonism severity (r[18] = 0.82, p < 0.001). Residual cell counts in lesioned nigra correlated linearly with peak dystonia scores (r[18] = -0.68, p=<0.001). Dystonia was not observed in monkeys without striatal dopamine depletion (n = 2); dystonia severity correlated with striatal dopamine depletion when residual nigral cell loss was less than 50% ([11] r = -0.83, p < 0.001) but spanned a broad range with near complete striatal dopamine depletion, when nigral cell loss was greater than 50%. Our data indicate that residual striatal dopamine may not reflect dystonia severity. We speculate on mechanisms of transient dystonia followed by parkinsonism that may be studied using this particular NHP MPTP model to better understand relationships of transient dystonia to nigrostriatal injury and parkinsonism.

非人灵长类动物单侧颈内动脉1-甲基-4-苯基-1,2,3,6-四氢吡啶(MPTP)输注引起短暂性对侧半肌张力障碍,随后出现稳定的对侧半帕金森病;肌张力障碍和帕金森氏症之间的关系尚不清楚。我们假设MPTP后短暂性肌张力障碍的严重程度与帕金森病的严重程度相关。在雄性猕猴nemestrina (n = 3)和M. fascularis (n = 17)中,我们给予单侧颈动脉内MPTP,然后将短暂峰值肌张力障碍和延迟性帕金森症的盲法评分进行关联。我们还将肌张力障碍的严重程度与死后纹状体残留多巴胺和神经神经元计数相关联,这些数据是在MPTP后平均53±15天获得的,在肌张力障碍消退后,但在稳定的帕金森病期间。肌张力障碍发作的中位潜伏期为1天,MPTP后的严重程度峰值为2.5天;肌张力障碍总持续时间为13.5天。帕金森病在MPTP后19.5天达到峰值,此后几乎保持不变。肌张力障碍峰值严重程度与帕金森病严重程度高度相关(r[18] = 0.82, p < 0.001)。受损黑质残余细胞计数与肌张力障碍峰值评分呈线性相关(r[18] = -0.68, p=n = 2);当残余的神经细胞丢失小于50%时,肌张力障碍的严重程度与纹状体多巴胺缺失相关([11]r = -0.83, p < 0.001),但当神经细胞丢失大于50%时,纹状体多巴胺几乎完全缺失,肌张力障碍的严重程度与纹状体多巴胺缺失的范围很宽。我们的数据表明残留纹状体多巴胺可能不能反映肌张力障碍的严重程度。我们推测帕金森病后短暂性肌张力障碍的机制,可以使用这个特殊的NHP MPTP模型来研究,以更好地理解短暂性肌张力障碍与黑质纹状体损伤和帕金森病的关系。
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引用次数: 0
Laminar VASO fMRI in focal hand dystonia patients. 局灶性手肌张力障碍患者的层间VASO功能磁共振成像。
Pub Date : 2023-01-01 DOI: 10.3389/dyst.2023.10806
Laurentius Huber, Panagiotis Kassavetis, Omer Faruk Gulban, Mark Hallett, Silvina G Horovitz

Focal Hand Dystonia (FHD) is a disabling movement disorder characterized by involuntary movements, cramps and spasms. It is associated with pathological neural microcircuits in the cortical somatosensory system. While invasive preclinical modalities allow researchers to probe specific neural microcircuits of cortical layers and columns, conventional functional magnetic resonance imaging (fMRI) cannot resolve such small neural computational units. In this study, we take advantage of recent developments in ultra-high-field MRI hardware and MR-sequences to capture altered digit representations and laminar processing in FHD patients. We aim to characterize the capability and challenges of layer-specific imaging and analysis tools in resolving laminar and columnar structures in clinical research setups. We scanned N = 4 affected and N = 5 unaffected hemispheres at 7T and found consistent results of altered neural microcircuitry in FHD patients: 1) In affected hemispheres of FHD patients, we found a breakdown of ordered finger representation in the primary somatosensory cortex, as suggested from previous low-resolution fMRI. 2) In affected primary motor cortices of FHD patients, we furthermore found increased fMRI activity in superficial cortico-cortical neural input layers (II/III), compared to relatively weaker activity in the cortico-spinal output layers (Vb/VI). Overall, we show that layer-fMRI acquisition and analysis tools have the potential to address clinically-driven neuroscience research questions about altered computational mechanisms at the spatial scales that were previously only accessible in animal models. We believe that this study paves the way for easier translation of preclinical work into clinical research in focal hand dystonia and beyond.

局灶性手肌张力障碍(FHD)是一种以不自主运动、痉挛和痉挛为特征的残疾运动障碍。它与皮层体感觉系统的病理神经微回路有关。虽然侵入性临床前模式允许研究人员探测皮层层和柱的特定神经微回路,但传统的功能磁共振成像(fMRI)无法解析如此小的神经计算单元。在这项研究中,我们利用超高场MRI硬件和MRI序列的最新发展来捕获FHD患者的手指表征和层流处理的改变。我们的目标是描述在解决层状和柱状结构的临床研究设置层特异性成像和分析工具的能力和挑战。我们在7T时扫描了N = 4个受影响的半球和N = 5个未受影响的半球,发现FHD患者神经微电路改变的结果一致:1)在FHD患者的受影响半球,我们发现初级体感皮层中有序的手指表征被破坏,这与之前的低分辨率fMRI显示的结果一致。2)在FHD患者受影响的初级运动皮质中,我们进一步发现皮质-皮质神经输入层(II/III)的fMRI活动增加,而皮质-脊髓输出层(Vb/VI)的活动相对较弱。总的来说,我们表明层- fmri采集和分析工具有潜力解决关于空间尺度上改变的计算机制的临床驱动的神经科学研究问题,这些问题以前只能在动物模型中获得。我们相信这项研究为将局灶性手肌张力障碍的临床前工作更容易转化为临床研究铺平了道路。
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引用次数: 0
Altered brain state during episodic dystonia in tottering mice decouples primary motor cortex from limb kinematics. 蹒跚学步的小鼠在发作性肌张力障碍期间大脑状态的改变使初级运动皮层与肢体运动学脱钩。
Pub Date : 2023-01-01 Epub Date: 2023-02-02 DOI: 10.3389/dyst.2023.10974
Madelyn M Gray, Anant Naik, Timothy J Ebner, Russell E Carter
Episodic Ataxia Type 2 (EA2) is a rare neurological disorder caused by a mutation in the CACNA1A gene, encoding the P/Q-type voltage-gated Ca2+ channel important for neurotransmitter release. Patients with this channelopathy exhibit both cerebellar and cerebral pathologies, suggesting the condition affects both regions. The tottering (tg/tg) mouse is the most commonly used EA2 model due to an orthologous mutation in the cacna1a gene. The tg/tg mouse has three prominent behavioral phenotypes: a dramatic episodic dystonia; absence seizures with generalized spike and wave discharges (GSWDs); and mild ataxia. We previously observed a novel brain state, transient low-frequency oscillations (LFOs) in the cerebellum and cerebral cortex under anesthesia. In this study, we examine the relationships among the dystonic attack, GSWDs, and LFOs in the cerebral cortex. Previous studies characterized LFOs in the motor cortex of anesthetized tg/tg mice using flavoprotein autofluorescence imaging testing the hypothesis that LFOs provide a mechanism for the paroxysmal dystonia. We sought to obtain a more direct understanding of motor cortex (M1) activity during the dystonic episodes. Using two-photon Ca2+ imaging to investigate neuronal activity in M1 before, during, and after the dystonic attack, we show that there is not a significant change in the activity of M1 neurons from baseline through the attack. We also conducted simultaneous, multi-electrode recordings to further understand how M1 cellular activity and local field potentials change throughout the progression of the dystonic attack. Neither putative pyramidal nor inhibitory interneuron firing rate changed during the dystonic attack. However, we did observe a near complete loss of GSWDs during the dystonic attack in M1. Finally, using spike triggered averaging to align simultaneously recorded limb kinematics to the peak Ca2+ response, and vice versa, revealed a reduction in the spike triggered average during the dystonic episodes. Both the loss of GSWDs and the reduction in the coupling suggest that, during the dystonic attack, M1 is effectively decoupled from other structures. Overall, these results indicate that the attack is not initiated or controlled in M1, but elsewhere in the motor circuitry. The findings also highlight that LFOs, GSWDs, and dystonic attacks represent three brain states in tg/tg mice.
发作性共济失调2型(EA2)是一种罕见的神经系统疾病,由CACNA1A基因突变引起,该基因编码对神经递质释放重要的P/Q型电压门控Ca2+通道。患有这种通道病的患者同时表现出小脑和大脑的病理,这表明这种情况影响了这两个区域。摇摇欲坠(tg/tg)小鼠是最常用的EA2模型,这是由于cacna1a基因的同源突变。tg/tg小鼠有三种突出的行为表型:剧烈的发作性肌张力障碍;伴有全身性棘波放电的缺席性癫痫发作(GSWDs);和轻度共济失调。我们之前观察到一种新的大脑状态,即麻醉下小脑和大脑皮层的瞬态低频振荡(LFO)。在这项研究中,我们检查了大脑皮层中的肌张力障碍发作、GSWDs和LFO之间的关系。先前的研究使用黄蛋白自发荧光成像对麻醉的tg/tg小鼠运动皮层中的LFO进行了表征,验证了LFO为阵发性肌张力障碍提供机制的假设。我们试图更直接地了解肌张力障碍发作期间的运动皮层(M1)活动。使用双光子Ca2+成像来研究肌张力障碍发作之前、期间和之后M1的神经元活动,我们发现从基线到发作,M1神经元的活动没有显著变化。我们还进行了同时的多电极记录,以进一步了解M1细胞活性和局部场电位在肌张力障碍发作的整个过程中是如何变化的。在肌张力障碍发作期间,假定的锥体细胞和抑制性中间神经元的放电速率都没有改变。然而,我们确实观察到,在M1的反乌托邦发作期间,GSWDs几乎完全丧失。最后,使用尖峰触发平均值将同时记录的肢体运动学与峰值Ca2+反应对齐,反之亦然,揭示了在肌张力障碍发作期间尖峰触发平均数的减少。GSWDs的损失和耦合的减少都表明,在反乌托邦攻击期间,M1与其他结构有效地解耦。总的来说,这些结果表明攻击不是在M1中发起或控制的,而是在电机电路的其他地方。研究结果还强调,LFO、GSWDs和肌张力障碍发作代表了tg/tg小鼠的三种大脑状态。
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引用次数: 0
Anatomical categorization of isolated non-focal dystonia: novel and existing patterns using a data-driven approach. 孤立性非局灶性肌张力障碍的解剖学分类:使用数据驱动方法的新模式和现有模式
Pub Date : 2023-01-01 Epub Date: 2023-06-08 DOI: 10.3389/dyst.2023.11305
J R Younce, R H Cascella, B D Berman, H A Jinnah, S Bellows, J Feuerstein, A Wagle Shukla, A Mahajan, F C F Chang, K R Duque, S Reich, S Pirio Richardson, A Deik, N Stover, J M Luna, S A Norris

According to expert consensus, dystonia can be classified as focal, segmental, multifocal, and generalized, based on the affected body distribution. To provide an empirical and data-driven approach to categorizing these distributions, we used a data-driven clustering approach to compare frequency and co-occurrence rates of non-focal dystonia in pre-defined body regions using the Dystonia Coalition (DC) dataset. We analyzed 1,618 participants with isolated non-focal dystonia from the DC database. The analytic approach included construction of frequency tables, variable-wise analysis using hierarchical clustering and independent component analysis (ICA), and case-wise consensus hierarchical clustering to describe associations and clusters for dystonia affecting any combination of eighteen pre-defined body regions. Variable-wise hierarchical clustering demonstrated closest relationships between bilateral upper legs (distance = 0.40), upper and lower face (distance = 0.45), bilateral hands (distance = 0.53), and bilateral feet (distance = 0.53). ICA demonstrated clear grouping for the a) bilateral hands, b) neck, and c) upper and lower face. Case-wise consensus hierarchical clustering at k = 9 identified 3 major clusters. Major clusters consisted primarily of a) cervical dystonia with nearby regions, b) bilateral hand dystonia, and c) cranial dystonia. Our data-driven approach in a large dataset of isolated non-focal dystonia reinforces common segmental patterns in cranial and cervical regions. We observed unexpectedly strong associations between bilateral upper or lower limbs, which suggests that symmetric multifocal patterns may represent a previously underrecognized dystonia subtype.

根据专家共识,肌张力障碍可根据受影响的身体分布分为局灶性、节段性、多灶性和全身性。为了提供一种经验和数据驱动的方法来对这些分布进行分类,我们使用数据驱动的聚类方法,使用肌张力障碍联盟(DC)数据集比较预定义身体区域中非局灶性肌张力障碍的频率和共现率。我们分析了来自DC数据库的1618名孤立性非局灶性肌张力障碍参与者。分析方法包括构建频率表、使用层次聚类和独立成分分析(ICA)的变量分析,以及描述肌张力障碍的关联和聚类的案例一致性层次聚类,这些关联和聚类影响18个预定义身体区域的任何组合。变量层次聚类显示双侧上肢(距离=0.40)、上下脸(距离=0.45)、双手(距离=0.53)和双脚(距离=0.73)之间的关系最为密切。ICA显示a)双手、b)颈部和c)上下脸之间的分组清晰。在k=9的情况下,一致性分层聚类确定了3个主要聚类。主要集群主要包括a)邻近区域的颈部肌张力障碍,b)双侧手部肌张力障碍和c)颅骨肌张力障碍。在一个孤立的非局灶性肌张力障碍的大型数据集中,我们的数据驱动方法强化了颅骨和颈部常见的节段模式。我们观察到双侧上肢或下肢之间出乎意料的强烈关联,这表明对称的多焦点模式可能代表了以前被低估的肌张力障碍亚型。
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引用次数: 0
Video analysis of patients with blepharospasm and lower face dystonias. 眼睑痉挛及下脸肌张力障碍患者的视频分析
Pub Date : 2023-01-01 Epub Date: 2023-06-15 DOI: 10.3389/dyst.2023.11385
Mahdieh Hosseini, Panagiotis Kassavetis, Mark Hallett

Background: Blepharospasm (BSP) is a focal dystonia. There is a lack of standardization in the length of time necessary to get a measure of BSP severity for rating scales.

Objectives: 1) Determine the difference between evaluating the number of eye closures in patients with blepharospasm in 1 vs. 2 min. 2) Characterize the prevalence, phenomenology and concordance of sensory trick in subjects with only blepharospasm compared to those with blepharospasm associated with other dystonias of the head.

Methods: Thirty-eight, 2-min-long standardized videos of subjects with BSP without any other dystonias were reviewed (group1). Eye closure rate was measured in 0-60 s vs. 60-120 s. Wilcoxon signed-rank test and Spearman correlation coefficient were used to compare the eye closure rate between these two intervals. An additional 68 standardized videos of subjects with blepharospasm associated with dystonia of the head were reviewed (group2). Presence, phenomenology and concordance between what subjects verbally reported as their sensory trick and what they demonstrated was classified for both groups then qualitatively compared.

Results/conclusion: Eye closure rates between 0-60 s and 0-120 s were not statistically different. There is no added benefit of counting the number of eye closures in 2 min, compared to 1 min, in patients with BSP. Sensory trick was reported by 57% of subjects with BSP and 80% of subjects who have blepharospasm and other dystonias of the head. With 100% and 97% concordance, patients' self-reported sensory trick accurately describes the movements that alleviate their dystonic movements.

背景:眼睑痉挛(BSP)是局灶性肌张力障碍。在获得评定量表的BSP严重程度的量度所需的时间长度方面缺乏标准化。目的:1)确定1分钟和2分钟内眼睑痉挛患者闭眼次数评估的差异。2)与伴有其他头部肌张力障碍的眼睑痉挛患者相比,仅眼睑痉挛患者感觉障碍的患病率、现象学和一致性。方法:回顾无其他肌张力障碍的BSP患者的38个2分钟的标准化视频(第一组)。测定0 ~ 60 s和60 ~ 120 s的闭眼率。采用Wilcoxon符号秩检验和Spearman相关系数比较两个区间的闭眼率。另外回顾了68个伴有头部肌张力障碍的眼睑痉挛患者的标准化视频(第二组)。存在,现象学和一致性在被试口头报告的感觉技巧和他们展示的之间被分为两组然后进行定性比较。结果/结论:0 ~ 60 s和0 ~ 120 s的闭眼率无统计学差异。与1分钟相比,BSP患者在2分钟内计算闭眼次数并没有额外的好处。57%的BSP患者和80%的眼睑痉挛和其他头部肌张力障碍患者报告有感觉障碍。与100%和97%的一致性,患者自我报告的感觉技巧准确地描述了减轻其张力障碍运动的运动。
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引用次数: 0
Subthalamic Nucleus Deep Brain Stimulation for Dystonia: Evidence, Pros and Cons 丘脑下核深部脑刺激治疗肌张力障碍:证据,赞成和反对
Pub Date : 2022-11-28 DOI: 10.3389/dyst.2022.10609
C. Kilbane, J. Ostrem
The primary target for deep brain stimulation (DBS) for medication refractory dystonia has traditionally been the globus pallidus internus (GPi), however alternate targets have also been explored with the hope they might offer similar or superior outcomes with less side effects and reduced battery demands. Recent studies have shown comparable outcomes with both pallidal and subthalamic (STN) DBS, although the level of evidence is still superior for the GPi. There may not be an “optimal target” for all dystonia patients, with both targets offering the potential for excellent control of dystonia but more comparison studies are needed. In this review, we will discuss the history, efficacy, as well as target specific benefits and possible side effects of STN DBS for dystonia.
传统上,深部脑刺激(DBS)治疗难治性肌张力障碍的主要靶点是内白球(GPi),然而,人们也在探索其他靶点,希望它们能提供类似或更好的结果,副作用更小,减少电池需求。最近的研究表明,尽管GPi的证据水平仍然优越,但pallidal和subthalamic DBS (STN)的结果相当。可能不存在一个适用于所有肌张力障碍患者的“最佳靶点”,两个靶点都提供了控制肌张力障碍的潜力,但需要更多的比较研究。在这篇综述中,我们将讨论STN DBS治疗肌张力障碍的历史、疗效、目标特异性益处和可能的副作用。
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引用次数: 0
期刊
Dystonia
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