Annals of Neurology · 2005 · 281 citations · 38 references
Life SciencesNeurologyNeuroscienceDementiaNeurochemistryNeurodegenerationAlzheimer DiseaseBiomarkers Of NeurodegenerationCognitive ImpairmentDementia BiomarkersNeurodegenerative DiseasesNeurodegenerative DisordersAmnestic ImpairmentBiomarkers Of Lipid Oxidative DamageLipid Peroxidation BiomarkersLipid Peroxidation MarkersNeurochemical BiomarkersOxidative Damage BiomarkersOxidative Stress In NeurodegenerationRedox Metabolism In Neurodegeneration
Multiple studies demonstrate that the brain in Alzheimer's disease (AD) contains extensive oxidative damage. Most of these studies used advanced-stage AD patients raising the question of whether oxidative damage is a late effect of neurodegeneration or precedes and contributes to the pathogenesis of AD. Here we describe F(2)-isoprostane (F(2)-IsoP) and F(4)-neuroprostane (F(4)-NP) levels in longitudinally followed, well documented autopsied normal control subjects and patients with amnestic mild cognitive impairment (MCI), and late-stage AD. Gas chromatography/negative ion chemical ionization/mass spectrometry was used to determine F(2)-IsoP and F(4)-NP levels. Significant increases in F(2)-IsoP levels were found in frontal, parietal and occipital lobes in MCI and late AD compared to controls but no significant differences were present between MCI and late AD. A significant increase in F(4)-NPs was present in parietal and occipital lobes in MCI compared to controls and a significant increase was present in these regions and hippocampus in late AD compared to controls. The only difference between MCI and late AD was significantly increased F(4)-NP in hippocampus in late AD. Our data indicate that lipid peroxidation is present in the brain of MCI patients and suggest that oxidative damage may play a role in the pathogenesis of AD.
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Clinical diagnosis of Alzheimer's disease
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