Cognitive impairment and Alzheimer's disease: Links with oxidative stress and cholesterol metabolism
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Sekler, Alejandra
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Cognitive impairment and Alzheimer's disease: Links with oxidative stress and cholesterol metabolism
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Abstract
Oxidative stress has be en implicated in the progression of a number of neurodegenerative
diseases, inc1uding Alzheimer's disease (AD), Parkinson's disease and amyotrophic lateral sclerosis.
We carried out a~ in-depth study of cognitive impainnent and its relationships with oxidative stress
markers such as ferric-reducing ability of plasma (FRAP), plasma malondialdehyde and total
antioxidative capacity (T AC), as well as cholesterol parameters, in two subsets ofsubjects, AD patients
(n = 59) and a control group ofneurologically normal subjects (n = 29), attending thc University
Hospital Salvador in Santiago, Chile. Cognitivc impairment was assessed by a sct of
neuropsychological tests (Mini-Mental State Examination, Boston Naming Test, Ideomotor Praxia by
imitatíoll, Semantic Verbal Fluency of animals or words with initial A, Test ofMcmory Alteration,
Frontal Asscssmcnt Battcry), whilc the levels ofthose oxidative stress markers and cholesterol
metabolism parameters were determined according with standard bioassays in fresh plasma samples of
the two subgroups of patients. No significant differences were observed when the cholesterol
parameters (low-, high-density lipoprotein, total cholesterol) of the AD group were compared with
normal controls. Interestingly, a correlation was evidenced when the levels of cognitive impairment
were analyzed with respect to the plasma antioxidant capacity (AOC) ofpatients. In this context, the
subset of subjects exhibiting cognitive impairment were divided into two subgroups according with
their Global Dementia Scale performance: a subgroup with mild AD and a subgroup with moderate to
severc AD. Significant differences in AOC were found between subgroups. The different correlations
between cognitive impainnent of subgroups of subjects with the oxidative stress profilc are discussed in
the context of AD pathogenesis.
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Research was supported by grants 1050198 and 1080254 from
FONDECYT, the International Center for Biomedicine (to
RBM) and by the Bicentennial Project IPC-79 of PBCT
-CONICYT (to AS). The authors report no conflicts of interest
in this work.
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Neuropsychiatric Disease and Treatment, 2008:4( 4) 715-722
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