Gouriou Estelle, Schneider Cyril
Noninvasive neurostimulation laboratory, Research center of CHU de Québec-Université Laval, Neuroscience Division, Quebec, Canada.
Faculty of Medicine, Université Laval, Quebec, Canada.
Heliyon. 2024 Aug 2;10(15):e35563. doi: 10.1016/j.heliyon.2024.e35563. eCollection 2024 Aug 15.
Noninvasive stimulation of the nervous system is of growing interest in Parkinson's disease (PD) to slow-down motor decline and decrease medication and its side-effects. Repetitive transcranial magnetic stimulation (rTMS) used in PD to modulate the excitability of the primary motor cortex (M1) provided controversial results, in part because of interactions with medication. This warrants to administer rTMS in drug-free patients. Repetitive peripheral magnetic stimulation (rPMS of muscles) has not yet been tested in PD. Its influence on M1 plasticity (as tested by TMS, transcranial magnetic stimulation) and sensorimotor disorders in other health conditions makes it worth be explored in PD. Thus, rTMS and rPMS were tested in a drug-free woman (52 years old, PD-diagnosed 10 years ago) in four different rTMS + rPMS combinations (one week apart): sham-sham, real-real, real-sham, sham-real. rTMS was applied over M1 contralateral to the most impaired bodyside, and rPMS on muscles of the legs, trunk, and arms, bilaterally. M1 plasticity (TMS measures) and motor symptoms and function (clinical outcomes) were measured at different timepoints. The real-real session induced the largest motor improvements, with possible summation of effects between sessions, and maintenance at follow-up (80 days later). This was paralleled by changes of M1 facilitation and inhibition. This sheds a new light on the link between TMS measures of M1 plasticity and motor changes in PD and informs on the remaining potential for neuroplasticity and functional improvement after 10 years of PD with no antiparkinsonian drug. De novo patients with PD (drug-free) should be motivated to participate in future randomized clinical trials to further test the slow-down or delay of motor decline under noninvasive neurostimulation regimens, whatever the stage of the disease.
在帕金森病(PD)中,非侵入性刺激神经系统以减缓运动功能衰退、减少药物使用及其副作用正受到越来越多的关注。重复经颅磁刺激(rTMS)用于PD以调节初级运动皮层(M1)的兴奋性,但结果存在争议,部分原因是与药物的相互作用。这就需要在未服用药物的患者中进行rTMS治疗。重复外周磁刺激(肌肉的rPMS)尚未在PD中进行测试。它对M1可塑性(通过经颅磁刺激(TMS)测试)以及其他健康状况下的感觉运动障碍的影响,使得其在PD中值得探索。因此,对一名未服用药物的女性(52岁,10年前被诊断为PD)进行了rTMS和rPMS测试,采用四种不同的rTMS + rPMS组合(间隔一周):假刺激-假刺激、真刺激-真刺激、真刺激-假刺激、假刺激-真刺激。rTMS施加于身体受损最严重一侧对侧的M1,rPMS双侧施加于腿部、躯干和手臂的肌肉。在不同时间点测量M1可塑性(TMS测量)以及运动症状和功能(临床结果)。真刺激-真刺激疗程带来了最大的运动改善,各疗程之间可能存在效果累加,并在随访(80天后)得以维持。这与M1易化和抑制的变化相平行。这为PD中M1可塑性的TMS测量与运动变化之间的联系提供了新的线索,并揭示了在未使用抗帕金森药物的情况下,PD病程10年后神经可塑性和功能改善的剩余潜力。新发PD(未服用药物)患者应被鼓励参与未来的随机临床试验,以进一步测试在非侵入性神经刺激方案下运动功能衰退的减缓或延迟情况,无论疾病处于何种阶段。