Pharmacological treatment of ALS

Neurol Neurochir Pol. 2001;35(1 Suppl):41-50.

Abstract

Amyotrophic lateral sclerosis (ALS) is a neurodegenerative disease resulting from chronic and selective loss of motor neurons in the brain and spinal cord. In 1993, the etiology of ALS has been clarified for a small sub-group of patients with an autosomal-dominant form of this disease. About 10 percent of familial ALS patients have been associated with more than 50 mutations of the gene of the Cu/Zn superoxide dismutase (SOD1). Mutations in the SOD1 gene account for 1 percent of all ALS patients and have therefore limited epidemological and clinical relevance; however, they are of fundamental importance for the understanding of the ALS pathogenesis, and the development of neuroprotective strategies. In two double-blind and placebo-controlled studies the membrane stabilisator riluzole has been shown to be the first neuroprotective compound with a significant effect on survival of ALS patients. The neuroprotective approach reduced therapeutic nihilism in ALS and is a first step in the treatment of this devastating disease.

Publication types

  • Review

MeSH terms

  • Amyotrophic Lateral Sclerosis / drug therapy*
  • Amyotrophic Lateral Sclerosis / genetics
  • Amyotrophic Lateral Sclerosis / pathology
  • Clinical Trials as Topic
  • Humans
  • Motor Neurons / pathology
  • Neuroprotective Agents / therapeutic use*
  • Point Mutation / genetics
  • Riluzole / therapeutic use*
  • Superoxide Dismutase / genetics

Substances

  • Neuroprotective Agents
  • Riluzole
  • Superoxide Dismutase