Annals of Clinical Neurophysiology

  • 제17권1호
  • /
  • Pages.1-16
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  • 2015
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  • 2508-691X(pISSN)
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  • 2508-6960(eISSN)
대한임상신경생리학회 (The Korean Society of Clinical Neurophysiology)
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근위축측삭경화증에 대한 치료약물 임상시험 현황

Update of Therapeutic Clinical Trials for Amyotrophic Lateral Sclerosis

  • 김남희 (동국대학교 일산병원 신경과) ;
  • 이민오 (동국대학교 일산병원 신경과)
  • Kim, Nam-Hee (Department of Neurology, Dongguk University Ilsan Hospital) ;
  • Lee, Min Oh (Department of Neurology, Dongguk University Ilsan Hospital)
  • 투고 : 2014.12.12
  • 심사 : 2015.05.29
  • 발행 : 2015.06.30
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초록

Amyotrophic lateral sclerosis (ALS) is a fatal neurodegenerative disease that is characterized by progressive death of motor neurons in the cortex, brainstem, and spinal cord. Until now, many treatment strategies have been tested in ALS, but so far only Riluzole has shown efficacy of slightly slowing disease progression. The pathophysiological mechanisms underlying ALS are multifactorial, with a complex interaction between genetic factors and molecular pathways. Other motor neuron disease such as spinal muscular atrophy (SMA) and spinobulbar muscular atrophy (SBMA) are also progressive neurodegenerative disease with loss of motor neuron as ALS. This common thread of motor neuron loss has provided a target for the development of therapies for these motor neuron diseases. A better understanding of these pathogenic mechanisms and the potential pathological relationship between the various cellular processes have suggested novel therapeutic approaches, including stem cell and genetics-based strategies, providing hope for feasible treatment of ALS.

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참고문헌

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