Human kallikrein 6 as a biomarker of Alzheimer's disease

Citation
Ep. Diamandis et al., Human kallikrein 6 as a biomarker of Alzheimer's disease, CLIN BIOCH, 33(8), 2000, pp. 663-667
Citations number
35
Categorie Soggetti
Medical Research Diagnosis & Treatment
Journal title
CLINICAL BIOCHEMISTRY
ISSN journal
00099120 → ACNP
Volume
33
Issue
8
Year of publication
2000
Pages
663 - 667
Database
ISI
SICI code
0009-9120(200011)33:8<663:HK6AAB>2.0.ZU;2-H
Abstract
Background: Alzheimer's disease (AD) is a major cause of dementia in the el derly. It is generally difficult to diagnose accurately early AD. A few bio markers, including tau protein and amyloid beta -42, are now used as aids f or diagnosis and monitoring of AD. Our aim was to examine the possible use of cerebrospinal fluid, blood and tissue, and human kallikrein 6 (hK6) conc entration as a marker of AD. Methods: We have used a highly sensitive and specific immunofluorometric pr ocedure for measuring hK6. We measured hK6 in tissue extracts from AD brain or normal individuals, in cerebrospinal fluids of AD patients or normals a nd in whole blood of AD patients and normals and compared the findings. We have used ten pairs of AD/normal controls in all cases. Results: We found that hK6 concentration is tissue extracts from AD brain w ere approximately twofold lower than extracts from normal controls. Further , we found that cerebrospinal fluid hK6 concentration is approximately a th reefold increase, in comparison to cerebrospinal fluid controls (p = 0.001) . We have also found that the whole blood hK6 concentration in AD patients is about ten times higher than hK6 concentration in normal controls (p = 0. 002). We have immunohistochemically localized the expression of hK6 in epit helial cells of the chorioid plexus. Conclusions: This is the first report describing significant elevations of cerebrospinal fluid and plasma and whole blood hK6 concentration in AD pati ents, in comparison to controls. These data suggest that hK6 may constitute a new biomarker for diagnosis and monitoring of AD. Copyright (C) 2001 The Canadian Society of Clinical Chemists.