Combining inhibitory and facilitatory repetitive transcranial magnetic stimulation (rTMS) treatment improves motor function by modulating GABA in acute ischemic stroke patients.

IF 1.9 4区 医学 Q4 NEUROSCIENCES
Qing-Mei Chen, Fei-Rong Yao, Hai-Wei Sun, Zhi-Guo Chen, Jun Ke, Juan Liao, Xiu-Ying Cai, Li-Qiang Yu, Zhen-Yan Wu, Zhi Wang, Xi Pan, Hao-Yu Liu, Li Li, Quan-Quan Zhang, Wei-Hua Ling, Qi Fang
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引用次数: 3

Abstract

Background: The combination of inhibitory and facilitatory repetitive transcranial magnetic stimulation (rTMS) can improve motor function of stroke patients with undefined mechanism. It has been demonstrated that rTMS exhibits a neuro-modulatory effect by regulating the major inhibitory neurotransmitter γ-aminobutyric acid (GABA) in other diseases.

Objectives: To evaluate the effect of combined inhibitory and facilitatory rTMS on GABA in the primary motor cortex (M1) for treating motor dysfunction after acute ischemic stroke.

Methods: 44 ischemic stroke patients with motor dysfunction were randomly divided into two groups. The treatment group was stimulated with 10 Hz rTMS at the ipsilesional M1 and 1 Hz rTMS at the contralesional M1. The sham group received bilateral sham stimulation at the motor cortices. The GABA level in the bilateral M1 was measured by proton magnetic resonance spectroscopy (1H-MRS) at 24 hours before and after rTMS stimulation. Motor function was measured using the Fugl-Meyer Assessment (FMA). The clinical assessments were performed before and after rTMS and after 3 months.

Results: The treatment group exhibited a greater improvement in motor function 24 hours after rTMS compared to the sham group. The increased improvement in motor function lasted for at least 3 months after treatment. Following 4 weeks of rTMS, the GABA level in the ipsilesional M1 of the treatment group was significantly decreased compared to the sham group. Furthermore, the change of FMA score for motor function was negatively correlated to the change of the GABA:Cr ratio. Finally, the effect of rTMS on motor function outcome was partially mediated by GABA level change in response to the treatment (27.7%).

Conclusions: Combining inhibitory and facilitatory rTMS can decrease the GABA level in M1, which is correlated to the improvement of motor function. Thus, the GABA level in M1 may be a potential biomarker for treatment strategy decisions regarding rTMS neuromodulatory interventions.

抑制性和促进性重复经颅磁刺激(rTMS)联合治疗通过调节GABA改善急性缺血性脑卒中患者的运动功能。
背景:抑制性和促进性重复经颅磁刺激(rTMS)联合应用可改善脑卒中患者的运动功能,但机制尚不明确。研究表明,rTMS通过调节其他疾病的主要抑制性神经递质γ-氨基丁酸(GABA)表现出神经调节作用。目的:探讨抑制和促进联用rTMS治疗急性缺血性卒中后运动功能障碍对初级运动皮质(M1) GABA的影响。方法:44例缺血性脑卒中运动功能障碍患者随机分为两组。治疗组在同侧M1和对侧M1分别施加10hz和1hz的rTMS刺激。假手术组接受双侧假手术运动皮质刺激。采用质子磁共振波谱法(1H-MRS)测定rTMS刺激前后24 h双侧M1中GABA水平。采用Fugl-Meyer评估法(FMA)测量运动功能。分别于rTMS前后及3个月后进行临床评估。结果:与假手术组相比,治疗组在rTMS后24小时运动功能有更大的改善。运动功能的改善持续治疗后至少3个月。经颅磁刺激4周后,治疗组同侧M1中GABA水平较假手术组明显降低。运动功能FMA评分的变化与GABA:Cr比值的变化呈负相关。最后,rTMS对运动功能结果的影响部分是由治疗后GABA水平的变化介导的(27.7%)。结论:抑制和促进相结合的rTMS可降低M1中GABA的水平,这与运动功能的改善有关。因此,M1中的GABA水平可能是rTMS神经调节干预治疗策略决策的潜在生物标志物。
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来源期刊
CiteScore
5.40
自引率
3.60%
发文量
22
审稿时长
>12 weeks
期刊介绍: This interdisciplinary journal publishes papers relating to the plasticity and response of the nervous system to accidental or experimental injuries and their interventions, transplantation, neurodegenerative disorders and experimental strategies to improve regeneration or functional recovery and rehabilitation. Experimental and clinical research papers adopting fresh conceptual approaches are encouraged. The overriding criteria for publication are novelty, significant experimental or clinical relevance and interest to a multidisciplinary audience. Experiments on un-anesthetized animals should conform with the standards for the use of laboratory animals as established by the Institute of Laboratory Animal Resources, US National Academy of Sciences. Experiments in which paralytic agents are used must be justified. Patient identity should be concealed. All manuscripts are sent out for blind peer review to editorial board members or outside reviewers. Restorative Neurology and Neuroscience is a member of Neuroscience Peer Review Consortium.
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