Peptides and proteins in plasma and cerebrospinal fluid as biomarkers for the prediction, diagnosis, and monitoring of therapeutic efficacy of Alzheimer's disease

被引:65
作者
Aluise, Christopher D.
Sowell, Rena A.
Butterfield, D. Allan [1 ]
机构
[1] Univ Kentucky, Ctr Membrane Sci, Dept Chem, Lexington, KY 40506 USA
来源
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR BASIS OF DISEASE | 2008年 / 1782卷 / 10期
关键词
Biomarker; Plasma; CSF; Alzheimer's disease;
D O I
10.1016/j.bbadis.2008.07.008
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
Alzheimer's disease (AD) affects millions of persons worldwide. Earlier detection and/or diagnosis of AD would permit earlier intervention, which conceivably could delay progression of this dementing disorder. In order to accomplish this goal, reliable and specific biomarkers are needed. Biomarkers are multidimensional and have the potential to aid in various facets of AD such as diagnostic prediction, assessment of disease stage, discrimination from normally cognitive controls as well as other forms of dementia. and therapeutic efficacy of AD drugs. To date, biomarker research has focused on plasma and cerebrospinal fluid (CSF), two bodily fluids believed to contain the richest source of biomarkers for AD. CSF is the fluid surrounding the central nervous system (CNS), and is the most indicative obtainable fluid of brain pathology. Blood plasma contains proteins that affect brain processes from the periphery, as well as proteins/peptides exported from the brain; this fluid would be ideal for biomarker discovery due to the ease and non-invasive process of sample collection. However, it seems reasonable that biomarker discovery will result in combinations of CSF, plasma, and other fluids such as urine, to serve the aforementioned purposes. This review focuses on proteins and peptides identified from CSF, plasma, and urine that may serve as biomarkers in AD. (C) 2008 Elsevier B.V. All rights reserved.
引用
收藏
页码:549 / 558
页数:10
相关论文
共 159 条
  • [1] The influence of diagnosis, intra- and inter-person variability on serum and plasma Aβ levels
    Abdullah, Laila
    Paris, Daniel
    Luis, Cheryl
    Quadros, Arnita
    Parrish, Julia
    Valdes, Luis
    Keegan, Andrew P.
    Mathura, Venkatarajan
    Crawford, Fiona
    Mullan, Michael
    [J]. NEUROSCIENCE LETTERS, 2007, 428 (2-3) : 53 - 58
  • [2] IMMUNOCHEMICAL IDENTIFICATION OF THE SERINE PROTEASE INHIBITOR ALPHA-1-ANTICHYMOTRYPSIN IN THE BRAIN AMYLOID DEPOSITS OF ALZHEIMERS-DISEASE
    ABRAHAM, CR
    SELKOE, DJ
    POTTER, H
    [J]. CELL, 1988, 52 (04) : 487 - 501
  • [3] Voluntary exercise decreases amyloid load in a transgenic model of Alzheimer's disease
    Adlard, PA
    Perreau, VM
    Pop, V
    Cotman, CW
    [J]. JOURNAL OF NEUROSCIENCE, 2005, 25 (17) : 4217 - 4221
  • [4] alpha 1-antichymotrypsin interaction with A beta(1-42) does not inhibit fibril formation but attenuates the peptide toxicity
    Aksenov, MY
    Aksenova, MV
    Carney, JM
    Butterfield, DA
    [J]. NEUROSCIENCE LETTERS, 1996, 217 (2-3) : 117 - 120
  • [5] alpha-1-Antichymotrypsin interaction with A beta (1-40) inhibits fibril formation but does not affect the peptide toxicity
    Aksenova, MV
    Aksenov, MY
    Butterfield, DA
    Carney, JM
    [J]. NEUROSCIENCE LETTERS, 1996, 211 (01) : 45 - 48
  • [6] Alzheimers Assoc, 1998, NEUROBIOL AGING, V19, P109
  • [7] Reductions in β-amyloid concentrations in vivo by the γ-secretase inhibitors BMS-289948 and BMS-299897
    Anderson, JJ
    Holtz, G
    Baskin, PP
    Turner, M
    Rowe, B
    Wang, BW
    Kounnas, MZ
    Lamb, BT
    Barten, D
    Felsenstein, K
    McDonald, I
    Srinivasan, K
    Munoz, B
    Wagner, SL
    [J]. BIOCHEMICAL PHARMACOLOGY, 2005, 69 (04) : 689 - 698
  • [8] Cerebrospinal fluid tau and Aβ42 as predictors of development of Alzheimer's disease in patients with mild cognitive impairment
    Andreasen, N
    Minthon, L
    Vanmechelen, E
    Vanderstichele, H
    Davidsson, P
    Winblad, B
    Blennow, K
    [J]. NEUROSCIENCE LETTERS, 1999, 273 (01) : 5 - 8
  • [9] Cerebrospinal fluid levels of total-tau, phospho-tau and Aβ42 predicts development of Alzheimer's disease in patients with mild cognitive impairment
    Andreasen, N
    Vanmechelen, E
    Vanderstichele, H
    Davidsson, P
    Blennow, K
    [J]. ACTA NEUROLOGICA SCANDINAVICA, 2003, 107 : 47 - 51
  • [10] Evaluation of CSF-tau and CSF-Aβ42 as diagnostic markers for Alzheimer disease in clinical practice
    Andreasen, N
    Minthon, L
    Davidsson, P
    Vanmechelen, E
    Vanderstichele, H
    Winblad, B
    Blennow, K
    [J]. ARCHIVES OF NEUROLOGY, 2001, 58 (03) : 373 - 379