Quantitative in vivo biomarkers of oxidative damage and their application to the diagnosis and management of Alzheimer's disease

Thomas J. Montine; Joseph F. Quinn; Kathleen S. Montine; Jeffrey A. Kaye; John C.S. Breitner

doi:10.3233/jad-2005-8405

Quantitative in vivo biomarkers of oxidative damage and their application to the diagnosis and management of Alzheimer's disease

Thomas J. Montine, Joseph F. Quinn, Kathleen S. Montine, Jeffrey A. Kaye, John C.S. Breitner

Research output: Contribution to journal › Article › peer-review

18 Scopus citations

Abstract

Dementia from Alzheimer's disease (AD) represents a significant and growing public health burden and presents a clear therapeutic imperative. Key to success in this undertaking will be biomarkers for the objective assessment of disease progression and response to therapeutics. Oxidative damage is one facet of AD pathogenesis for which there are experimentally validated quantitative in vivo biomarkers, the F₂-isoprostanes (IsoPs). While plasma- or urine-based assays are desirable, consistent and reproducible cross-sectional data for increased F₂-IsoPs in AD and mild cognitive impairment have been obtained only for CSF. In addition, measurement of CSF F₂-IsoPs can increase the accuracy of laboratory-based classification of geriatric dementias, and have been used to assess objectively the response to anti-oxidant interventions in AD.

Original language	English (US)
Pages (from-to)	359-367
Number of pages	9
Journal	Journal of Alzheimer's Disease
Volume	8
Issue number	4
DOIs	https://doi.org/10.3233/jad-2005-8405
State	Published - Jan 1 2005
Externally published	Yes

Keywords

Alzheimer's disease
Biomarkers
F2-isoprostanes
Oxidative stress

ASJC Scopus subject areas

Neuroscience(all)
Clinical Psychology
Geriatrics and Gerontology
Psychiatry and Mental health

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10.3233/jad-2005-8405

Cite this

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abstract = "Dementia from Alzheimer's disease (AD) represents a significant and growing public health burden and presents a clear therapeutic imperative. Key to success in this undertaking will be biomarkers for the objective assessment of disease progression and response to therapeutics. Oxidative damage is one facet of AD pathogenesis for which there are experimentally validated quantitative in vivo biomarkers, the F2-isoprostanes (IsoPs). While plasma- or urine-based assays are desirable, consistent and reproducible cross-sectional data for increased F2-IsoPs in AD and mild cognitive impairment have been obtained only for CSF. In addition, measurement of CSF F2-IsoPs can increase the accuracy of laboratory-based classification of geriatric dementias, and have been used to assess objectively the response to anti-oxidant interventions in AD.",

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AU - Kaye, Jeffrey A.

AU - Breitner, John C.S.

PY - 2005/1/1

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Quantitative in vivo biomarkers of oxidative damage and their application to the diagnosis and management of Alzheimer's disease

Abstract

Keywords

ASJC Scopus subject areas

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