Familial amyotrophic lateral sclerosis (ALS) in Japan associated with H46R mutation in Cu Zn superoxide dismutase gene

A possible new subtype of familial ALS

Masashi Aoki, Masahito Ogasawara, Yoichi Matsubara, Kuniaki Narisawa, Shozo Nakamura, Yasuto Itoyama, Koji Abe

Research output: Contribution to journalArticle

94 Citations (Scopus)

Abstract

Amyotrophic lateral sclerosis (ALS) is a progressive and fatal neurological disorder that results in relentless damage to the motor neuron system. Although about 5-10% of cases are familial, the pathophysiologic process of ALS remains unknown. We identified a novel point mutation A to G in exon 2 of the Cu Zn SOD gene, resulting in an amino acid substitution of histidine46 by arginine (H46R), in two Japanese familial ALS (FALS) families. The segregations of the mutation were evident. The enzymatic activities of Cu Zn SOD of peripheral red blood cell lysate were reduced to about 80% in the affected members, compared with other non-affected family members. The patients in these families are clinically characterized by relative late onset, initial involvement in lower extremities, relative rare impairment of bulbar muscles and much slow progression of muscular weakness and atrophy, compared with other Japanese FALS cases who have no mutation in the Cu Zn SOD gene. These findings suggest that the H46R mutation in Cu Zn SOD gene is highly related to this unique subtype of FALS.

Original languageEnglish
Pages (from-to)77-83
Number of pages7
JournalJournal of the Neurological Sciences
Volume126
Issue number1
DOIs
Publication statusPublished - 1994
Externally publishedYes

Fingerprint

Japan
Amyotrophic Lateral Sclerosis
Mutation
Genes
Muscular Atrophy
Muscle Weakness
Motor Neurons
Amino Acid Substitution
Nervous System Diseases
Point Mutation
Arginine
Lower Extremity
Exons
Erythrocytes
Muscles
Amyotrophic lateral sclerosis 1
Superoxide Dismutase-1

Keywords

  • Cu Zn superoxide dismutase gene
  • Familial ALS
  • Mutation
  • Subtype

ASJC Scopus subject areas

  • Ageing
  • Clinical Neurology
  • Surgery
  • Neuroscience(all)
  • Developmental Neuroscience
  • Neurology

Cite this

Familial amyotrophic lateral sclerosis (ALS) in Japan associated with H46R mutation in Cu Zn superoxide dismutase gene : A possible new subtype of familial ALS. / Aoki, Masashi; Ogasawara, Masahito; Matsubara, Yoichi; Narisawa, Kuniaki; Nakamura, Shozo; Itoyama, Yasuto; Abe, Koji.

In: Journal of the Neurological Sciences, Vol. 126, No. 1, 1994, p. 77-83.

Research output: Contribution to journalArticle

Aoki, Masashi ; Ogasawara, Masahito ; Matsubara, Yoichi ; Narisawa, Kuniaki ; Nakamura, Shozo ; Itoyama, Yasuto ; Abe, Koji. / Familial amyotrophic lateral sclerosis (ALS) in Japan associated with H46R mutation in Cu Zn superoxide dismutase gene : A possible new subtype of familial ALS. In: Journal of the Neurological Sciences. 1994 ; Vol. 126, No. 1. pp. 77-83.
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abstract = "Amyotrophic lateral sclerosis (ALS) is a progressive and fatal neurological disorder that results in relentless damage to the motor neuron system. Although about 5-10{\%} of cases are familial, the pathophysiologic process of ALS remains unknown. We identified a novel point mutation A to G in exon 2 of the Cu Zn SOD gene, resulting in an amino acid substitution of histidine46 by arginine (H46R), in two Japanese familial ALS (FALS) families. The segregations of the mutation were evident. The enzymatic activities of Cu Zn SOD of peripheral red blood cell lysate were reduced to about 80{\%} in the affected members, compared with other non-affected family members. The patients in these families are clinically characterized by relative late onset, initial involvement in lower extremities, relative rare impairment of bulbar muscles and much slow progression of muscular weakness and atrophy, compared with other Japanese FALS cases who have no mutation in the Cu Zn SOD gene. These findings suggest that the H46R mutation in Cu Zn SOD gene is highly related to this unique subtype of FALS.",
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AB - Amyotrophic lateral sclerosis (ALS) is a progressive and fatal neurological disorder that results in relentless damage to the motor neuron system. Although about 5-10% of cases are familial, the pathophysiologic process of ALS remains unknown. We identified a novel point mutation A to G in exon 2 of the Cu Zn SOD gene, resulting in an amino acid substitution of histidine46 by arginine (H46R), in two Japanese familial ALS (FALS) families. The segregations of the mutation were evident. The enzymatic activities of Cu Zn SOD of peripheral red blood cell lysate were reduced to about 80% in the affected members, compared with other non-affected family members. The patients in these families are clinically characterized by relative late onset, initial involvement in lower extremities, relative rare impairment of bulbar muscles and much slow progression of muscular weakness and atrophy, compared with other Japanese FALS cases who have no mutation in the Cu Zn SOD gene. These findings suggest that the H46R mutation in Cu Zn SOD gene is highly related to this unique subtype of FALS.

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