Biomarkers Obtained by Transcranial Magnetic Stimulation of the Motor Cortex in Epilepsy

被引:20
|
作者
Tsuboyama, Melissa [1 ,2 ]
Kaye, Harper Lee [1 ,2 ]
Rotenberg, Alexander [1 ,2 ,3 ]
机构
[1] Boston Childrens Hosp, Dept Neurol, Div Epilepsy & Clin Neurophysiol, Neuromodulat Program, Boston, MA 02115 USA
[2] Boston Childrens Hosp, Dept Neurol, FM Kirby Neurobiol Ctr, Boston, MA 02115 USA
[3] Beth Israel Deaconess Med Ctr, Berenson Allen Ctr Noninvas Brain Stimulat, Boston, MA 02215 USA
来源
基金
美国国家卫生研究院;
关键词
biomarker (development); transcranial magnetic stimulation (TMS); epilepsy-abnormalities; classification; drug therapy; drug development and application; neuromodulation; motor cortex excitability; THETA-BURST STIMULATION; CORTICAL EXCITABILITY; SILENT PERIOD; SEIZURE SUPPRESSION; SINGLE-PULSE; DOUBLE-BLIND; IN-VIVO; INHIBITION; SAFETY; BRAIN;
D O I
10.3389/fnint.2019.00057
中图分类号
B84 [心理学]; C [社会科学总论]; Q98 [人类学];
学科分类号
03 ; 0303 ; 030303 ; 04 ; 0402 ;
摘要
Epilepsy is associated with numerous neurodevelopmental disorders. Transcranial magnetic stimulation (TMS) of the motor cortex coupled with electromyography (EMG) enables biomarkers that provide measures of cortical excitation and inhibition that are particularly relevant to epilepsy and related disorders. The motor threshold (MT), cortical silent period (CSP), short interval intracortical inhibition (SICI), intracortical facilitation (ICF), and long interval intracortical inhibition (LICI) are among TMS-derived metrics that are modulated by antiepileptic drugs. TMS may have a practical role in optimization of antiepileptic medication regimens, as studies demonstrate dose-dependent relationships between TMS metrics and acute medication administration. A close association between seizure freedom and normalization of cortical excitability with long-term antiepileptic drug use highlights a plausible utility of TMS in measures of anti-epileptic drug efficacy. Finally, TMS-derived biomarkers distinguish patients with various epilepsies from healthy controls and thus may enable development of disorder-specific biomarkers and therapies both within and outside of the epilepsy realm.
引用
收藏
页数:10
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