Abstract | OBJECTIVE: DNA damage accumulation in brain is associated with the development of Alzheimer disease (AD), but newly identified protein markers of DNA damage have not been evaluated in the diagnosis of AD and other forms of dementia. METHODS: RESULTS: Enzymatic activity of chitinase ( chitotriosidase activity) and stathmin protein level were significantly increased in CSF of patients with AD and non-AD dementia compared with that of no dementia control patients. As a single marker, chitinase activity was most powerful for distinguishing patients with AD from no dementia patients with an accuracy of 85.8% using a single threshold. Discrimination was even superior to clinically standard CSF markers that showed an accuracy of 78.4% (β- amyloid) and 77.6% (tau). Combined analysis of chitinase with other markers increased the accuracy to a maximum of 91%. The biomarkers of DNA damage were also increased in CSF of patients with non-AD dementia compared with no dementia patients, and the new biomarkers improved the diagnosis of non-AD dementia as well as the discrimination of AD from non-AD dementia. CONCLUSIONS: Taken together, the findings in this study provide experimental evidence that DNA damage markers are significantly increased in AD and non-AD dementia. The biomarkers identified outperformed the standard CSF markers for diagnosing AD and non-AD dementia in the cohort investigated.
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Authors | M Watabe-Rudolph, Z Song, L Lausser, C Schnack, Y Begus-Nahrmann, M-O Scheithauer, G Rettinger, M Otto, H Tumani, D R Thal, J Attems, K A Jellinger, H A Kestler, C A F von Arnim, K L Rudolph |
Journal | Neurology
(Neurology)
Vol. 78
Issue 8
Pg. 569-77
(Feb 21 2012)
ISSN: 1526-632X [Electronic] United States |
PMID | 22323746
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Chemical References |
- Biomarkers
- Peptide Elongation Factor 1
- Stathmin
- Hexosaminidases
- Chitinases
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Topics |
- Adult
- Aged
- Aged, 80 and over
- Alzheimer Disease
(cerebrospinal fluid, diagnosis, enzymology)
- Biomarkers
(cerebrospinal fluid)
- Chitinases
(cerebrospinal fluid)
- DNA Damage
(physiology)
- Dementia
(cerebrospinal fluid, diagnosis, enzymology)
- Diagnosis, Differential
- Female
- Hexosaminidases
(cerebrospinal fluid)
- Humans
- Male
- Middle Aged
- Peptide Elongation Factor 1
(cerebrospinal fluid)
- Stathmin
(cerebrospinal fluid)
- Telomere
(physiology)
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