1 Department of Neurology, University of Colorado Anschutz Medical Campus, Denver, CO USA.
Brain. 2013 Dec;136(Pt 12):3645-58. doi: 10.1093/brain/awt282. Epub 2013 Oct 21.
Writer's cramp is a task-specific focal hand dystonia characterized by involuntary excessive muscle contractions during writing. Although abnormal striatal dopamine receptor binding has been implicated in the pathophysiology of writer's cramp and other primary dystonias, endogenous dopamine release during task performance has not been previously investigated in writer's cramp. Using positron emission tomography imaging with the D2/D3 antagonist 11C-raclopride, we analysed striatal D2/D3 availability at rest and endogenous dopamine release during sequential finger tapping and speech production tasks in 15 patients with writer's cramp and 15 matched healthy control subjects. Compared with control subjects, patients had reduced 11C-raclopride binding to D2/D3 receptors at rest in the bilateral striatum, consistent with findings in previous studies. During the tapping task, patients had decreased dopamine release in the left striatum as assessed by reduced change in 11C-raclopride binding compared with control subjects. One cluster of reduced dopamine release in the left putamen during tapping overlapped with a region of reduced 11C-raclopride binding to D2/D3 receptors at rest. During the sentence production task, patients showed increased dopamine release in the left striatum. No overlap between altered dopamine release during speech production and reduced 11C-raclopride binding to D2/D3 receptors at rest was seen. Striatal regions where D2/D3 availability at rest positively correlated with disease duration were lateral and non-overlapping with striatal regions showing reduced D2/D3 receptor availability, except for a cluster in the left nucleus accumbens, which showed a negative correlation with disease duration and overlapped with striatal regions showing reduced D2/D3 availability. Our findings suggest that patients with writer's cramp may have divergent responses in striatal dopamine release during an asymptomatic motor task involving the dystonic hand and an unrelated asymptomatic task, sentence production. Our voxel-based results also suggest that writer's cramp may be associated with reduced striatal dopamine release occuring in the setting of reduced D2/D3 receptor availability and raise the possibility that basal ganglia circuits associated with premotor cortices and those associated with primary motor cortex are differentially affected in primary focal dystonias.
书写痉挛是一种特定于任务的手部局灶性肌张力障碍,其特征是在书写过程中出现不自主的过度肌肉收缩。尽管异常纹状体多巴胺受体结合已被认为与书写痉挛和其他原发性肌张力障碍的病理生理学有关,但在书写痉挛患者中,任务执行期间的内源性多巴胺释放尚未被先前研究过。使用正电子发射断层扫描成像和 D2/D3 拮抗剂 11C-racopride,我们分析了 15 名书写痉挛患者和 15 名匹配的健康对照者在静息状态下纹状体 D2/D3 可用性以及在连续手指敲击和言语产生任务期间的内源性多巴胺释放。与对照组相比,患者双侧纹状体的 11C-racopride 与 D2/D3 受体的结合在静息时减少,这与先前的研究结果一致。在敲击任务中,与对照组相比,患者左纹状体的多巴胺释放减少,这通过 11C-racopride 结合减少来评估。在敲击过程中,左壳核中一个多巴胺释放减少的簇与静息时 D2/D3 受体结合减少的区域重叠。在句子产生任务中,患者的左纹状体多巴胺释放增加。在言语产生过程中改变的多巴胺释放与静息时 11C-racopride 与 D2/D3 受体的结合之间没有重叠。在静息时 D2/D3 可用性与疾病持续时间呈正相关的纹状体区域与显示 D2/D3 受体可用性降低的纹状体区域侧向且不重叠,除了左伏隔核的一个簇,该簇与疾病持续时间呈负相关并与显示 D2/D3 受体可用性降低的纹状体区域重叠。我们的研究结果表明,书写痉挛患者在涉及痉挛手的无症状运动任务和无关的无症状任务(句子产生)期间,纹状体多巴胺释放可能会出现不同的反应。我们的体素基结果还表明,书写痉挛可能与纹状体多巴胺释放减少有关,这种情况发生在 D2/D3 受体可用性降低的情况下,并提出基底节回路与运动前皮质相关的回路和与原发性运动皮质相关的回路在原发性局灶性肌张力障碍中可能受到不同影响的可能性。