論文

査読有り 国際誌
2019年10月

Low-dose perampanel improves refractory cortical myoclonus by the dispersed and suppressed paroxysmal depolarization shifts in the sensorimotor cortex.

Clinical neurophysiology : official journal of the International Federation of Clinical Neurophysiology
  • Kazuki Oi
  • Shuichiro Neshige
  • Takefumi Hitomi
  • Katsuya Kobayashi
  • Maya Tojima
  • Masao Matsuhashi
  • Akihiro Shimotake
  • Daiki Fujii
  • Riki Matsumoto
  • Shuhei Kasama
  • Masutaro Kanda
  • Yoshiaki Wada
  • Hirofumi Maruyama
  • Ryosuke Takahashi
  • Akio Ikeda
  • 全て表示

130
10
開始ページ
1804
終了ページ
1812
記述言語
英語
掲載種別
研究論文(学術雑誌)
DOI
10.1016/j.clinph.2019.07.006

OBJECTIVE: To elucidate the effects of perampanel (PER) on refractory cortical myoclonus for dose, etiology and somatosensory-evoked potential (SEP) findings. METHODS: We examined 18 epilepsy patients with seizure and cortical myoclonus. Based on data accumulated before and after PER treatment, correlations among clinical scores in myoclonus and activities of daily life (ADL); early cortical components of SEP; and PER blood concentration, were analyzed. RESULTS: PER (mean dose: 3.2 ± 2.1 mg/day) significantly improved seizures, myoclonus and ADL and significantly decreased the amplitude of and prolonged latency of giant SEP components. The degree of P25 and N33 prolongations (23.8 ± 1.6 to 24.7 ± 1.7 ms and 32.1 ± 4.0 to 33.7 ± 3.4 ms) were significantly correlated with improved ADL score (p = 0.019 and p = 0.025) and blood PER concentration (p = 0.011 and p = 0.025), respectively. CONCLUSIONS: Low-dose PER markedly improved myoclonus and ADL in patients with refractory cortical myoclonus. Our results suggest that SEP, particularly P25 latency, can be used as a potential biomarker for assessing the objective effects of PER on intractable cortical myoclonus. SIGNIFICANCE: In this study, PER lessened the degree of synchronized discharges in the postsynaptic neurons in the primary motor cortex.

リンク情報
DOI
https://doi.org/10.1016/j.clinph.2019.07.006
PubMed
https://www.ncbi.nlm.nih.gov/pubmed/31401489
Scopus
https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85070191984&origin=inward
Scopus Citedby
https://www.scopus.com/inward/citedby.uri?partnerID=HzOxMe3b&scp=85070191984&origin=inward
ID情報
  • DOI : 10.1016/j.clinph.2019.07.006
  • ISSN : 1388-2457
  • eISSN : 1872-8952
  • PubMed ID : 31401489
  • SCOPUS ID : 85070191984

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