Idebenone treatment in Friedreich's ataxia: neurological, cardiac, and biochemical monitoring

Neurology. 2003 May 27;60(10):1679-81. doi: 10.1212/01.wnl.0000068549.52812.0f.

Abstract

The authors report 1-year prospective data on eight patients with Friedreich ataxia. Idebenone did not halt the progression of ataxia. At the end of therapy, cardiac ultrasound demonstrated significant reduction of cardiac hypertrophy in six of eight patients. Cardiac strain and strain rate imaging showed that the reduction of hypertrophy is preceded by an early and linear improvement in cardiac function. Idebenone reduced erythrocyte protoporphyrin IX levels in five of six patients with elevated baseline levels; however, changes did not consistently relate to cardiac improvement.

Publication types

  • Clinical Trial
  • Randomized Controlled Trial
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adolescent
  • Adult
  • Benzoquinones / pharmacology
  • Benzoquinones / therapeutic use*
  • Cardiomyopathy, Hypertrophic / drug therapy
  • Cardiomyopathy, Hypertrophic / etiology
  • Cardiomyopathy, Hypertrophic / physiopathology
  • Child
  • Erythrocytes / chemistry
  • Female
  • Frataxin
  • Free Radical Scavengers / pharmacology
  • Free Radical Scavengers / therapeutic use*
  • Free Radicals
  • Friedreich Ataxia / blood
  • Friedreich Ataxia / complications*
  • Friedreich Ataxia / genetics
  • Friedreich Ataxia / physiopathology
  • Humans
  • Hypertrophy, Left Ventricular / drug therapy*
  • Hypertrophy, Left Ventricular / etiology
  • Hypertrophy, Left Ventricular / physiopathology
  • Iron-Binding Proteins / genetics
  • Iron-Binding Proteins / physiology
  • Male
  • Mitochondria / metabolism
  • Oxidative Stress
  • Prospective Studies
  • Protoporphyrins / blood
  • Stroke Volume
  • Ubiquinone / analogs & derivatives

Substances

  • Benzoquinones
  • Free Radical Scavengers
  • Free Radicals
  • Iron-Binding Proteins
  • Protoporphyrins
  • Ubiquinone
  • protoporphyrin IX
  • idebenone