Abstract |
To seek for a new valid biomarker using non-invasive specimens for the diagnosis of Alzheimer's disease (AD) and mild cognitive impairment (MCI), we carried out the detection of amyloid beta (Abeta) protein in urine. Ten-millilitre urine samples were first sedimented with trichloroacetic acid, and the pellets were resuspended for further analysis by Western blotting with anti-Abeta antibody. The detection sensitivity of the method was 40pg/ml. Rates of subjects positive for monomeric Abeta according to their clinical dementia rating (CDR) were 11.1% for CDR 0, 62.5% for CDR 0.5, 83.3% for CDR 1, 54.5% for CDR 2 and 0% for CDR 3. A single Abeta band relative to the CDR score reflects an alteration in the production, solubility and clearance of Abeta in the brain. Thus, the method could be used as both a diagnostic and monitoring tool in assessing AD and MCI patients during disease-modifying therapies.
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Authors | Manabu Takata, Manabu Nakashima, Taro Takehara, Hideyo Baba, Kazuyuki Machida, Yoshiharu Akitake, Kazuhiko Ono, Masato Hosokawa, Mitsuo Takahashi |
Journal | Neuroscience letters
(Neurosci Lett)
Vol. 435
Issue 2
Pg. 126-30
(Apr 18 2008)
ISSN: 0304-3940 [Print] Ireland |
PMID | 18343031
(Publication Type: Comparative Study, Journal Article)
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Chemical References |
- Amyloid beta-Peptides
- Peptide Fragments
- amyloid beta-protein (1-42)
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Topics |
- Aged
- Aged, 80 and over
- Alzheimer Disease
(urine)
- Amyloid beta-Peptides
(urine)
- Cognition Disorders
(urine)
- Female
- Humans
- Male
- Middle Aged
- Peptide Fragments
(urine)
- Severity of Illness Index
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