Oxidative stress in patients with Friedreich ataxia

被引:260
作者
Schulz, JB
Dehmer, T
Schöls, L
Mende, H
Hardt, C
Vorgerd, M
Bürk, K
Matson, W
Dichgan, J
Beal, MF
Bogdanov, MB
机构
[1] Univ Tubingen, Dept Neurol, D-72076 Tubingen, Germany
[2] Univ Tubingen, Sch Med, D-72074 Tubingen, Germany
[3] Ruhr Univ Bochum, St Josef Hosp, Dept Neurol, D-4630 Bochum, Germany
[4] Univ Essen Gesamthsch, Dept Human Genet, D-4300 Essen 1, Germany
[5] Ruhr Univ Bochum, Bergmannsheil Hosp, Dept Neurol, D-4630 Bochum, Germany
[6] ESA Inc, Chelmsford, MA USA
[7] Weill Med Col, Dept Neurol, New York, NY USA
[8] Weill Med Col, Dept Neurosci, New York, NY USA
[9] Cornell Univ, New York, NY USA
[10] New York Presbyterian Hosp, New York, NY USA
关键词
D O I
10.1212/WNL.55.11.1719
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
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.
引用
收藏
页码:1719 / 1721
页数:3
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