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Heart 2002;87:346-349; doi:10.1136/heart.87.4.346
Copyright © 2002 BMJ Publishing Group Ltd & British Cardiovascular Society
Heart 2002;87:346-349
© 2002 by Heart

CARDIOVASCULAR MEDICINE

Idebenone and reduced cardiac hypertrophy in Friedreich's ataxia

A O Hausse1, Y Aggoun1, D Bonnet1, D Sidi1, A Munnich2, A Rötig2, P Rustin2

1 Service de Cardiologie Pédiatrique, Hôpital Necker-Enfants Malades, 149 rue de Sévres, Paris, France
2 Unité de Recherches sur les Handicaps Génétiques de l'Enfant (INSERM U393), Hôpital Necker-Enfants Malades

Correspondence to:
Correspondence to:
Dr Arnold Munnich, INSERM U393, Hôpital Necker-Enfants Malades, 149 rue de Sévres, 75015 Paris, France;
munnich{at}necker.fr

Background: Friedreich's ataxia encodes a protein of unknown function, frataxin. The loss of frataxin is caused by a large GAA trinucleotide expansion in the first intron of the gene, resulting in deficiency of a Krebs cycle enzyme, aconitase, and of three mitochondrial respiratory chain complexes (I–III). This causes oxidative stress. Idebenone, a short chain quinone acting as an antioxidant, has been shown to protect heart muscle against oxidative stress in some patients.

Objective: To assess the efficiency of idebenone on cardiac hypertrophy in Friedreich's ataxia.

Design: Prospective, open trial.

Setting: Tertiary care centre.

Methods: Idebenone (5 mg/kg/day) was given orally to 38 patients with Friedreich's ataxia aged 4–22 years (20 males, 18 females). Cardiac ultrasound indices were recorded before and after idebenone treatment.

Results: After six months, cardiac ultrasound indicated a reduction in left ventricular mass of more than 20% in about half the patients (p < 0.001). The shortening fraction was initially reduced in six of the 38 patients (by between 11–26%) and it improved in five of these. In one patient, the shortening fraction only responded to 10 mg/kg/day of idebenone. No correlation was found between responsiveness to idebenone and age, sex, initial ultrasound indices, or the number of GAA repeats in the frataxin gene.

Conclusions: Idebenone is effective at controlling cardiac hypertrophy in Friedreich's ataxia. As the drug has no serious side effects, there is a good case for giving it continuously in a dose of 5–10 mg/kg/day in patients with Friedreich's ataxia at the onset of hypertrophic cardiomyopathy.

Keywords: hypertrophic cardiomyopathy; Friedreich's ataxia; idebenone; respiratory chain defect


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