Oxidative stress in patients with Friedreich ataxia

Increased generation of reactive oxygen species may underlie the pathophysiology of Friedreich ataxia (FRDA). The authors measured concentrations of 8-hydroxy-2'-deoxyguanosine (8OH2'dG), a marker of oxidative DNA damage, in urine and of dihydroxybenzoic acid (DHBA), a marker of hydroxyl r...

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Veröffentlicht in:Neurology 2000-12, Vol.55 (11), p.1719-1721
Hauptverfasser: SCHULZ, J. B, DEHMER, T, BOGDANOV, M. B, SCHÖLS, L, MENDE, H, HARDT, C, VORGERD, M, BÜRK, K, MATSON, W, DICHGANS, J, BEAL, M. F
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Sprache:eng
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Zusammenfassung:Increased generation of reactive oxygen species may underlie the pathophysiology of Friedreich ataxia (FRDA). The authors measured concentrations of 8-hydroxy-2'-deoxyguanosine (8OH2'dG), a marker of oxidative DNA damage, in urine and of dihydroxybenzoic acid (DHBA), a marker of hydroxyl radical attack, in plasma of 33 patients with FRDA. They found a 2.6-fold increase in normalized urinary 8OH2'dG but no change in plasma DHBA as compared with controls. Oral treatment with 5 mg/kg/day of the antioxidant idebenone for 8 weeks significantly decreased urinary 8OH2'dG concentrations, indicating that 8OH2'dG may be useful in monitoring therapeutic interventions in patients with FRDA.-1721
ISSN:0028-3878
1526-632X
DOI:10.1212/WNL.55.11.1719