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利用经颅磁刺激(TMS)探究脑-体连接:验证一种有望提供神经可塑性和中枢神经系统功能生物标志物的工具。

Probing the Brain-Body Connection Using Transcranial Magnetic Stimulation (TMS): Validating a Promising Tool to Provide Biomarkers of Neuroplasticity and Central Nervous System Function.

作者信息

Chaves Arthur R, Snow Nicholas J, Alcock Lynsey R, Ploughman Michelle

机构信息

L.A. Miller Centre, Recovery and Performance Laboratory, Faculty of Medicine, Memorial University of Newfoundland, St. John's, NL A1A 1E5, Canada.

出版信息

Brain Sci. 2021 Mar 17;11(3):384. doi: 10.3390/brainsci11030384.

DOI:10.3390/brainsci11030384
PMID:33803028
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8002717/
Abstract

Transcranial magnetic stimulation (TMS) is a non-invasive method used to investigate neurophysiological integrity of the human neuromotor system. We describe in detail, the methodology of a single pulse TMS protocol that was performed in a large cohort of people ( = 110) with multiple sclerosis (MS). The aim was to establish and validate a core-set of TMS variables that predicted typical MS clinical outcomes: walking speed, hand dexterity, fatigue, and cognitive processing speed. We provide a brief and simple methodological pipeline to examine excitatory and inhibitory corticospinal mechanisms in MS that map to clinical status. Delayed and longer ipsilateral silent period (a measure of transcallosal inhibition; the influence of one brain hemisphere's activity over the other), longer cortical silent period (suggestive of greater corticospinal inhibition via GABA) and higher resting motor threshold (lower corticospinal excitability) most strongly related to clinical outcomes, especially when measured in the hemisphere corresponding to the weaker hand. Greater interhemispheric asymmetry (imbalance between hemispheres) correlated with poorer performance in the greatest number of clinical outcomes. We also show, not surprisingly, that TMS variables related more strongly to motor outcomes than non-motor outcomes. As it was validated in a large sample of patients with varying severities of central nervous system dysfunction, the protocol described herein can be used by investigators and clinicians alike to investigate the role of TMS as a biomarker in MS and other central nervous system disorders.

摘要

经颅磁刺激(TMS)是一种用于研究人类神经运动系统神经生理完整性的非侵入性方法。我们详细描述了在一大群(n = 110)多发性硬化症(MS)患者中进行的单脉冲TMS方案的方法。目的是建立并验证一组预测典型MS临床结果的TMS变量核心集:步行速度、手部灵活性、疲劳和认知处理速度。我们提供了一个简短而简单的方法流程,以检查MS中与临床状态相关的兴奋性和抑制性皮质脊髓机制。延迟且较长的同侧静息期(胼胝体抑制的一种测量;一个脑半球活动对另一个脑半球的影响)、较长的皮质静息期(提示通过GABA有更强的皮质脊髓抑制)和较高的静息运动阈值(较低的皮质脊髓兴奋性)与临床结果的相关性最强,尤其是在对应较弱手的半球中进行测量时。更大的半球间不对称(半球之间的不平衡)与最多临床结果中的较差表现相关。我们还表明,不出所料,TMS变量与运动结果的相关性比与非运动结果的相关性更强。由于该方案在大量不同严重程度的中枢神经系统功能障碍患者样本中得到了验证,本文所述的方案可供研究人员和临床医生用于研究TMS作为MS和其他中枢神经系统疾病生物标志物的作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9526/8002717/88d70476d87d/brainsci-11-00384-g010.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9526/8002717/1045eaf79e7f/brainsci-11-00384-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9526/8002717/86eb8e598f65/brainsci-11-00384-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9526/8002717/8d2f11019480/brainsci-11-00384-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9526/8002717/850a24729294/brainsci-11-00384-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9526/8002717/c28d390d89d7/brainsci-11-00384-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9526/8002717/e3fe4c0c9aa4/brainsci-11-00384-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9526/8002717/4222ed85f702/brainsci-11-00384-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9526/8002717/790f11a68ea0/brainsci-11-00384-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9526/8002717/01ef01ebb391/brainsci-11-00384-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9526/8002717/88d70476d87d/brainsci-11-00384-g010.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9526/8002717/1045eaf79e7f/brainsci-11-00384-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9526/8002717/86eb8e598f65/brainsci-11-00384-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9526/8002717/8d2f11019480/brainsci-11-00384-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9526/8002717/850a24729294/brainsci-11-00384-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9526/8002717/c28d390d89d7/brainsci-11-00384-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9526/8002717/e3fe4c0c9aa4/brainsci-11-00384-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9526/8002717/4222ed85f702/brainsci-11-00384-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9526/8002717/790f11a68ea0/brainsci-11-00384-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9526/8002717/01ef01ebb391/brainsci-11-00384-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9526/8002717/88d70476d87d/brainsci-11-00384-g010.jpg

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