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.
引用
收藏
页码:653 / 661
页数:9
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