Dagan Moria, Herman Talia, Mirelman Anat, Giladi Nir, Hausdorff Jeffrey M
Center for the Study of Movement, Cognition and Mobility, Neurological Institute, Tel Aviv Sourasky Medical Center, 6 Weizmann Street, Tel Aviv, Israel.
Sagol School of Neuroscience, Tel Aviv University, Tel Aviv, Israel.
Exp Brain Res. 2017 Aug;235(8):2463-2472. doi: 10.1007/s00221-017-4981-9. Epub 2017 May 16.
Freezing of Gait (FOG) is one of the most debilitating gait impairments in Parkinson's disease (PD), leading to increased fall risk and reduced health-related quality of life. The utility of parkinsonian medications is often limited in the case of FOG and it frequently becomes dopamine resistant. Recent studies have suggested that pre-frontal cortex (PFC) dysfunction contributes to FOG; however, most previous findings provide only indirect evidence. To better understand the role of the PFC, we aimed to investigate the impact of high frequency, deep, repetitive transcranial magnetic stimulation (drTMS) of the medial PFC on FOG and its mediators. Nine patients with advanced PD participated in a randomized, cross-over exploratory study. We applied drTMS over the medial PFC for 16 weeks, with real and sham conditions; each condition included an intensive (i.e., 3 times a week) phase and a maintenance (once a week) phase. Scores on a FOG-provoking test, the motor part of the Unified Parkinson's Disease Rating Scale, and gait variability significantly improved after real drTMS, but not after the sham condition. Self-report of FOG severity and cognitive scores did not improve. Due to discomfort and pain during treatment, two patients dropped out and the study was halted. These initial findings support the cause-and-effect role of the pre-frontal cortex in FOG among patients with PD. Due to the small sample size, findings should be interpreted cautiously. Further studies are needed to more fully assess the role of the medial PFC in the underlying mechanism of FOG and the possibility of using non-invasive brain stimulation to modify FOG.
冻结步态(FOG)是帕金森病(PD)中最使人衰弱的步态障碍之一,会导致跌倒风险增加和与健康相关的生活质量下降。在冻结步态的情况下,帕金森病药物的效用往往有限,并且它经常对多巴胺产生抗性。最近的研究表明,前额叶皮质(PFC)功能障碍导致了冻结步态;然而,大多数先前的研究结果仅提供了间接证据。为了更好地理解前额叶皮质的作用,我们旨在研究内侧前额叶皮质高频、深部、重复经颅磁刺激(drTMS)对冻结步态及其介导因素的影响。9名晚期帕金森病患者参与了一项随机交叉探索性研究。我们在内侧前额叶皮质应用drTMS 16周,包括真实刺激和假刺激条件;每种条件都包括一个强化(即每周3次)阶段和一个维持(每周1次)阶段。在真实drTMS后,冻结步态激发试验、统一帕金森病评定量表的运动部分以及步态变异性的评分显著改善,但在假刺激条件下没有改善。冻结步态严重程度的自我报告和认知评分没有改善。由于治疗期间的不适和疼痛,两名患者退出,研究停止。这些初步研究结果支持了前额叶皮质在帕金森病患者冻结步态中的因果作用。由于样本量小,研究结果应谨慎解释。需要进一步研究以更全面地评估内侧前额叶皮质在冻结步态潜在机制中的作用以及使用非侵入性脑刺激改善冻结步态的可能性。