Comparative proteomics of cerebrospinal fluid in neuropathologically-confirmed Alzheimer's disease and non-demented elderly subjects

• Published in: Neurological research (New York) 2006-03, Vol.28 (2), p.155-163
• Main Authors: Castaño, Eduardo M., Roher, Alex E., Esh, Chera L., Kokjohn, Tyler A., Beach, Thomas
• Format: Article
• Language: English
• Subjects: Aged; Aged, 80 and over; Aging - metabolism; Alzheimer Disease - cerebrospinal fluid; Alzheimer Disease - diagnosis; Alzheimer Disease - physiopathology; ALZHEIMER'S DISEASE; Amyloid beta-Peptides - metabolism; Apolipoprotein A-I - analysis; Apolipoprotein A-I - cerebrospinal fluid; BIOMARKERS; Biomarkers - analysis; Biomarkers - cerebrospinal fluid; Brain - metabolism; Brain - pathology; Brain - physiopathology; Cathepsin D - analysis; Cathepsin D - cerebrospinal fluid; CEREBROSPINAL FLUID; Electrophoresis, Gel, Two-Dimensional; Eye Proteins - analysis; Eye Proteins - cerebrospinal fluid; Female; Hemopexin - analysis; Hemopexin - cerebrospinal fluid; Humans; Male; Mass Spectrometry; Nerve Growth Factors - analysis; Nerve Growth Factors - cerebrospinal fluid; Nerve Tissue Proteins - analysis; Nerve Tissue Proteins - cerebrospinal fluid; Prealbumin - analysis; Prealbumin - cerebrospinal fluid; Predictive Value of Tests; PROTEOMICS; Proteomics - methods; Reference Values; Serpins - analysis; Serpins - cerebrospinal fluid
• ISSN: 0161-6412; 1743-1328
• DOI: 10.1179/016164106X98035

Objectives: Diagnostic tests able to reveal Alzheimer's disease (AD) in living patients before cognitive ability is destroyed are urgently needed. Such tests must distinguish AD from other dementia causes, as well as differentiate subtle changes associated with normal aging from true pathology emergence. A single biomarker offering such diagnostic and prognostic capacities has eluded identification. Therefore, a valuable test for AD is likely to be based on a specific pattern of change in a set of proteins, rather than a single protein. Methods: We examined pooled cerebrospinal fluid (CSF) samples obtained from neuropathologically-confirmed AD (n=43) and non-demented control subjects (n=43) using 2-dimensional gel electrophoresis (2DE) proteomic methodology to detect differentially expressed proteins. Proteins exhibiting expression level differences between the pools were recovered and identified using matrix-assisted laser desorption/ionization-time of flight (MALDI-TOF) mass spectrometry. Results: Five differentially-expressed proteins with potential roles in amyloid-β metabolism and vascular and brain physiology [apolipoprotein A-1 (Apo A-1), cathepsin D (CatD), hemopexin (HPX), transthyretin (TTR), and two pigment epithelium-derived factor (PEDF) isoforms] were identified. Apo A-1, CatD and TTR were significantly reduced in the AD pool sample, while HPX and the PEDF isoforms were increased in AD CSF. Discussion: These results suggest that multi-factor proteomic pattern analysis of the CSF may provide a means to diagnose and assess AD.