Maillet Audrey, Thobois Stéphane, Fraix Valérie, Redouté Jérôme, Le Bars Didier, Lavenne Franck, Derost Philippe, Durif Franck, Bloem Bastiaan R, Krack Paul, Pollak Pierre, Debû Bettina
Université Joseph Fourier, Grenoble Universités, Grenoble, France; INSERM-UJF-CEA-CHU U836 Grenoble Institut des Neurosciences, Grenoble, France; Centre de Neuroscience Cognitive, UMR 5229 CNRS, Lyon, France.
Hum Brain Mapp. 2015 Mar;36(3):959-80. doi: 10.1002/hbm.22679. Epub 2014 Nov 19.
Gait disturbances, including freezing of gait, are frequent and disabling symptoms of Parkinson's disease. They often respond poorly to dopaminergic treatments. Although recent studies have shed some light on their neural correlates, their modulation by dopaminergic treatment remains quite unknown. Specifically, the influence of levodopa on the networks involved in motor imagery (MI) of parkinsonian gait has not been directly studied, comparing the off and on medication states in the same patients. We therefore conducted an [H2 (15) 0] Positron emission tomography study in eight advanced parkinsonian patients (mean disease duration: 12.3 ± 3.8 years) presenting with levodopa-responsive gait disorders and FoG, and eight age-matched healthy subjects. All participants performed three tasks (MI of gait, visual imagery and a control task). Patients were tested off, after an overnight withdrawal of all antiparkinsonian treatment, and on medication, during consecutive mornings. The order of conditions was counterbalanced between subjects and sessions. Results showed that imagined gait elicited activations within motor and frontal associative areas, thalamus, basal ganglia and cerebellum in controls. Off medication, patients mainly activated premotor-parietal and pontomesencephalic regions. Levodopa increased activation in motor regions, putamen, thalamus, and cerebellum, and reduced premotor-parietal and brainstem involvement. Areas activated when patients are off medication may represent compensatory mechanisms. The recruitment of these accessory circuits has also been reported for upper-limb movements in Parkinson's disease, suggesting a partly overlapping pathophysiology between imagined levodopa-responsive gait disorders and appendicular signs. Our results also highlight a possible cerebellar contribution in the pathophysiology of parkinsonian gait disorders through kinesthetic imagery.
步态障碍,包括步态冻结,是帕金森病常见且致残的症状。它们对多巴胺能治疗的反应往往不佳。尽管最近的研究对其神经关联有了一些了解,但多巴胺能治疗对它们的调节作用仍然相当不清楚。具体而言,左旋多巴对帕金森病步态运动想象(MI)所涉及网络的影响尚未在同一患者的未服药和服药状态下进行直接研究。因此,我们对8名患有左旋多巴反应性步态障碍和步态冻结的晚期帕金森病患者(平均病程:12.3±3.8年)和8名年龄匹配的健康受试者进行了一项[H2(15)0]正电子发射断层扫描研究。所有参与者都执行三项任务(步态运动想象、视觉想象和一项对照任务)。患者在连续的早晨进行测试,一次是在停用所有抗帕金森病治疗过夜后处于未服药状态,另一次是在服药状态下。条件的顺序在受试者和测试时段之间进行了平衡。结果表明,在对照组中,想象步态会引起运动和额叶联合区、丘脑、基底神经节和小脑的激活。未服药时,患者主要激活运动前区 - 顶叶和脑桥中脑区域。左旋多巴增加了运动区域、壳核、丘脑和小脑的激活,并减少了运动前区 - 顶叶和脑干的参与。患者未服药时激活的区域可能代表补偿机制。在帕金森病上肢运动中也报道了这些辅助回路的募集,这表明想象的左旋多巴反应性步态障碍和肢体症状之间存在部分重叠的病理生理学。我们的结果还强调了通过动觉想象,小脑在帕金森病步态障碍病理生理学中可能发挥的作用。