Cerebrospinal fluid F2-isoprostane levels are increased in Alzheimer's disease

被引:200
作者
Montine, TJ
Markesbery, WR
Morrow, JD
Roberts, LJ
机构
[1] Vanderbilt Univ, Med Ctr, Dept Pathol, Nashville, TN 37232 USA
[2] Vanderbilt Univ, Med Ctr, Dept Med, Nashville, TN 37232 USA
[3] Vanderbilt Univ, Med Ctr, Dept Pharmacol, Nashville, TN 37232 USA
[4] Vanderbilt Univ, Med Ctr, Ctr Mol Neurosci, Nashville, TN 37232 USA
[5] Univ Kentucky, Med Ctr, Sanders Brown Ctr Aging, Lexington, KY USA
关键词
D O I
10.1002/ana.410440322
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Postmortem studies have associated Alzheimer's disease (AD) with regionally increased oxidative damage to brain. Lacking, however, is a specific marker of oxidative damage to brain that may be measured during life. We tested the hypothesis that cerebrospinal fluid (CSF) concentrations of F-2-isoprostanes (F-2-IsoPs), stable products of arachidonate peroxidation, are increased in CSF of AD patients. CSF from lateral ventricles (VF) was analyzed from 11 AD patients and 11 control subjects who participated in a rapid autopsy program. VF F-2-IsoP concentrations were significantly elevated in AD patients compared with control subjects (72 +/- 7 vs 46 +/- 4 pg/ml) and were significantly linearly correlated with brain weight (-0.3 pg/ml/g, r(2) = 0.32). These results suggest that quantification of CSF F-2-IsoP concentrations may provide a useful biomarker of central nervous system oxidative damage in AD.
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页码:410 / 413
页数:4
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