Human Motor Control Section, National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, Maryland 20892-1428.
Chulalongkorn Center of Excellence for Parkinson's Disease & Related Disorders, Department of Medicine, Faculty of Medicine, Chulalongkorn University and King Chulalongkorn Memorial Hospital, Thai Red Cross Society, Bangkok, 10330, Thailand.
J Neurosci. 2020 Nov 25;40(48):9317-9326. doi: 10.1523/JNEUROSCI.1181-20.2020. Epub 2020 Oct 23.
There are two types of dystonic tremor syndromes (DTS), dystonic tremor (DT) and tremor associated with dystonia (TAWD), and neither is understood. DTS likely share some mechanisms with nontremulous dystonia, and there may also be overlaps with essential tremor (ET). We studied 21 ET (8 females, 13 males) and 22 DTS human patients (10 females, 12 males), including 13 human patients with DT (writer's cramp with writing tremor) and 9 human patients with tremor associated with dystonia (TAWD; cervical dystonia with hand tremor). Tremors were analyzed using accelerometry and surface EMG of the antagonist pairs of arm muscles during posture, simple kinetic movement, and writing. Cerebellar inhibition was performed to assess cerebello-thalamo-cortical involvement. DT exhibited higher variability of peak frequency and greater instability of tremor burst intervals over time (higher tremor stability index) than ET or TAWD regardless of tasks. Intermuscular coherence magnitude between the antagonist pairs increased during the writing task in DT, but not ET or TAWD. ET and TAWD exhibited different phase relationships of the temporal fluctuations of voluntary movement and tremor in the kinetic condition. A linear discriminant classifier based on these tremor parameters was able to distinguish the three groups with a classification accuracy of 95.1%. Cerebellar inhibition was significantly reduced in DT, but not in TAWD, compared with ET and healthy controls. Our study shows that the two DTS are distinct entities with DT closer to nontremorous dystonia and TAWD closer to ET. This study provides novel findings about characteristics and pathophysiology of the two different types of dystonic tremor syndromes compared with essential tremor. Patients with DTS are classified into DT who have dystonia and tremor in the same area, and tremor associated with dystonia (TAWD) who have dystonia and tremor elsewhere. Our results showed that DT exhibits increased tremor variability, instability, and intermuscular coherence, and decreased cerebello-thalamo-cortical inhibition compared with TAWD. Our study shows that DT and TAWD are distinct phenotypes, and that the physiological characteristics of DT are more similar to nontremorous dystonia, and TAWD is closer to ET.
有两种类型的肌张力障碍性震颤综合征(DTS),即肌张力障碍性震颤(DT)和震颤伴肌张力障碍(TAWD),两者都不被理解。DTS 可能与非震颤性肌张力障碍具有某些共同机制,并且与特发性震颤(ET)也可能存在重叠。我们研究了 21 例 ET(8 名女性,13 名男性)和 22 例 DTS 人类患者(10 名女性,12 名男性),包括 13 例 DT 人类患者(书写痉挛伴书写震颤)和 9 例震颤伴肌张力障碍患者(颈肌张力障碍伴手部震颤)。使用加速度计和手臂拮抗肌的表面肌电图分析姿势、简单动力运动和书写时的震颤。进行小脑抑制以评估小脑-丘脑-皮质的受累情况。无论任务如何,DT 的峰值频率变异性更高,震颤爆发间隔的时间稳定性更差(更高的震颤稳定性指数),而 ET 或 TAWD 则不是。在书写任务中,DT 拮抗肌对之间的肌间相干性幅度增加,但 ET 或 TAWD 则不然。在动力条件下,ET 和 TAWD 表现出自愿运动和震颤的时间波动的不同相位关系。基于这些震颤参数的线性判别分类器能够以 95.1%的分类准确率区分这三组。与 ET 和健康对照组相比,DT 的小脑抑制明显降低,但 TAWD 则不然。我们的研究表明,这两种 DTS 是不同的实体,DT 更接近非震颤性肌张力障碍,而 TAWD 更接近 ET。与特发性震颤相比,本研究提供了关于两种不同类型的肌张力障碍性震颤综合征的特征和病理生理学的新发现。DTS 患者分为 DT 患者,他们在同一区域具有肌张力障碍和震颤,以及震颤伴肌张力障碍(TAWD)患者,他们在其他地方具有肌张力障碍和震颤。我们的结果表明,与 TAWD 相比,DT 表现出更高的震颤变异性、不稳定性和肌间相干性,以及更低的小脑-丘脑-皮质抑制。我们的研究表明,DT 和 TAWD 是不同的表型,DT 的生理特征更类似于非震颤性肌张力障碍,而 TAWD 更接近 ET。