Stability of CSF [beta]-Amyloid1-42 and Tau Levels by APOE Genotype in Alzheimer Patients

Background: Cerebrospinal fluid (CSF) measures of β-amyloid1-42 and tau differ between patients with Alzheimer's Disease (AD) and elderly normal controls. The effect of time and APOE genotype on these biomarkers continues to be elucidated. Methods: We assessed CSF β-amyloid1-42 and tau in 20 mi...

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Veröffentlicht in:Dementia and geriatric cognitive disorders 2006-06, Vol.22 (1), p.48
Hauptverfasser: Huey, Edward D, Mirza, Nadeem, Putnam, Karen T, Soares, Holly, Csako, Gyorgy, Levy, James A, Copenhaver, Brittany, Cohen, Robert M, Sunderland, Trey
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Sprache:eng
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Zusammenfassung:Background: Cerebrospinal fluid (CSF) measures of β-amyloid1-42 and tau differ between patients with Alzheimer's Disease (AD) and elderly normal controls. The effect of time and APOE genotype on these biomarkers continues to be elucidated. Methods: We assessed CSF β-amyloid1-42 and tau in 20 mild-to-moderate AD patients, 11 APOE ε4+ and 9 APOE ε4-, over a mean time of 3.8 years (range 1-11.1 years). Results: Over the period measured, CSF β-amyloid1-42 levels were lower in APOE ε4+ compared to APOE ε4- patients, and the levels decreased over time. Tau levels were stable over time and did not show an effect of APOE allele. Conclusions: While this is a limited clinical sample, the further decrease in CSF β-amyloid1-42 (i.e., more abnormal) combined with the CSF tau stability over a mean period of almost 4 years suggests that β-amyloid1-42 and tau maintain their potential usefulness as diagnostic biomarkers over time. These findings should be taken into account if CSF β-amyloid1-42 and tau are used as measures of treatment response. Copyright © 2006 S. Karger AG, Basel
ISSN:1420-8008
1421-9824