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Dkk-3 is elevated in CSF and plasma of Alzheimer's disease patients
被引:40
作者:
Zenzmaier, Christoph
[1
]
Marksteiner, Josef
[2
]
Kiefer, Andreas
[3
]
Berger, Peter
[1
]
Humpel, Christian
[4
]
机构:
[1] Austrian Acad Sci, Inst Biomed Aging Res, A-6020 Innsbruck, Austria
[2] Landeskrankenhaus Klagenfurt, Dept Psychiat & Psychotherapy, Klagenfurt, Austria
[3] Landeskrankenhaus Klagenfurt, Inst Pathol, Klagenfurt, Austria
[4] Innsbruck Med Univ, Lab Psychiat & Exp Alzheimers Res, Dept Psychiat, Innsbruck, Austria
基金:
奥地利科学基金会;
关键词:
beta-amyloid (1-42);
Alzheimer's disease;
CSF;
Dickkopf-3;
p-tau-181;
tau;
MILD COGNITIVE IMPAIRMENT;
CEREBROSPINAL-FLUID;
ENDOTHELIAL-CELLS;
EARLY-DIAGNOSIS;
BIOMARKERS;
DEMENTIA;
PROTEINS;
DICKKOPF-3;
MODULATORS;
PATHWAY;
D O I:
10.1111/j.1471-4159.2009.06158.x
中图分类号:
Q5 [生物化学];
Q7 [分子生物学];
学科分类号:
071010 ;
081704 ;
摘要:
Biomarkers in CSF can offer improved diagnostic accuracy for Alzheimer's disease (AD). The present study investigated whether the glycoprotein and putative tumor suppressor Dickkopf homolog 3 (Dkk-3) is secreted into CSF and evaluated its applicability as a diagnostic marker for AD. Using our highly specific immunoenzymometric assay, Dkk-3 levels were measured in plasma and/or CSF of patients suffering from depression, mild cognitive impairment (MCI), or AD and compared with healthy subjects. Dkk-3 identity was verified by western blot and matrix-assisted laser desorption/ionization time-of-flight (MALDI-TOF) mass spectrometry (MS)/MS. High concentrations of Dkk-3 were detected in CSF compared with plasma (28.2 +/- 1.3 vs. 1.22 +/- 0.04 nmol/L, respectively). Consistently Dkk-3 expression was demonstrated in neurons of the cortex and epithelial cells of the choroid plexus, the major source of CSF. Significantly increased Dkk-3 levels in plasma and CSF were observed for AD patients compared with healthy subjects but not patients suffering from MCI or depression. In summary, our data indicate that elevated Dkk-3 levels are specifically associated with AD and might serve as a potential non-invasive AD biomarker in plasma.
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页码:653 / 661
页数:9
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