HOMEPRODUCTSCOMPANYCONTACTFAQResearchDictionaryPharmaSign Up FREE or Login

Chitinase enzyme activity in CSF is a powerful biomarker of Alzheimer disease.

AbstractOBJECTIVE:
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:
Here, we analyzed the level of novel biomarkers of DNA damage and telomere dysfunction (chitinase activity, N-acetyl-glucosaminidase activity, stathmin, and EF-1α) in CSF of 94 patients with AD, 41 patients with non-AD dementia, and 40 control patients without dementia.
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.
AuthorsM 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
JournalNeurology (Neurology) Vol. 78 Issue 8 Pg. 569-77 (Feb 21 2012) ISSN: 1526-632X [Electronic] United States
PMID22323746 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • Biomarkers
  • Peptide Elongation Factor 1
  • Stathmin
  • Hexosaminidases
  • Chitinases
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)

Join CureHunter, for free Research Interface BASIC access!

Take advantage of free CureHunter research engine access to explore the best drug and treatment options for any disease. Find out why thousands of doctors, pharma researchers and patient activists around the world use CureHunter every day.
Realize the full power of the drug-disease research graph!


Choose Username:
Email:
Password:
Verify Password:
Enter Code Shown: