Familial Amyotrophic Lateral Sclerosis

Naoki Suzuki, Ayumi Nishiyama, Masaaki Kato, Hitoshi Warita, Masashi Aoki

Research output: Contribution to journalReview articlepeer-review

3 Citations (Scopus)

Abstract

Amyotrophic lateral sclerosis (ALS) is the most rapidly progressive motor neuron disease (MND) in adults, characterized by the selective death of motor neurons in the motor cortex, brainstem, and spinal cord. Riluzole and edaravone are the only approved drugs available in Japan to date. Approximately 10% of ALS cases are familial in rature, defined as the existence of disease-causing mutation. SOD1 is the most frequent causative gene for ALS among Japanese individuals, while C9orf72 mutation is more prevalent in Western countries. Genotype-phenotype correlation described in the literature of familial ALS enables to establish models of the disease. This review article describes the clinical characteristics of familial ALS based on each disease-causing mutation. The pathomechanism of ALS including proteostasis, RNA metabolism, and axonal pathology are discussed in detail. We also reviewed the status of development of therapeutic strategies for familial ALS based on analysis of animal models and induced pluripotent stem cells.

Original languageEnglish
Pages (from-to)1169-1181
Number of pages13
JournalBrain and nerve = Shinkei kenkyu no shinpo
Volume71
Issue number11
DOIs
Publication statusPublished - 2019 Nov 1

ASJC Scopus subject areas

  • Clinical Neurology

Fingerprint

Dive into the research topics of 'Familial Amyotrophic Lateral Sclerosis'. Together they form a unique fingerprint.

Cite this