CSF biomarkers for mild cognitive impairment and early Alzheimer's disease

被引:143
作者
Andreasen, N
Blennow, K
机构
[1] Karolinska Univ Hosp, Geriatr Med Sect, Dept NEUROTEC, Karolinska Inst, SE-41486 Stockholm, Sweden
[2] Gothenburg Univ, Sahlgrenska Acad, Sect Expt Neurosci, Dept Clin Neurosci, Gothenburg, Sweden
关键词
biomarkers; CSF; MCI; AD;
D O I
10.1016/j.clineuro.2004.10.011
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
A correct clinical diagnosis, early in the course of Alzheimer's disease (AD), is of importance given the currently available symptomatic treatment with acetylcholine esterase inhibitors. The development of disease-modifying drugs like beta-sheet breakers or gamma- and beta-secretase inhibitors, emphasizes the need of improved diagnostic accuracy, especially in patients with mild cognitive impairment (MCI) that have incipient AD. Therefore, diagnostic markers in the cerebrospinal fluid (CSF) have become a rapidly growing research field. Three cerebrospinal fluid biomarkers (the 42 amino acid form of beta-amyloid (A beta), total tau, and phospho tau) have been evaluated in numerous scientific papers. These CSF markers have high sensitivity to differentiate early and incipient AD from normal aging, depression, alcohol dementia and Parkinson's disease, but lower specificity against other dementias, such as frontotemporal and Lewy body dementia. If these biomarkers are used in combination with a careful medical history, clinical examination, standard laboratory tests and imaging techniques of the brain, the diagnostic accuracy may be appropriate for the clinical evaluation of MCI cases. (c) 2004 Elsevier B.V. All rights reserved.
引用
收藏
页码:165 / 173
页数:9
相关论文
共 98 条
[1]   Cerebrospinal fluid tau and Aβ42 as predictors of development of Alzheimer's disease in patients with mild cognitive impairment [J].
Andreasen, N ;
Minthon, L ;
Vanmechelen, E ;
Vanderstichele, H ;
Davidsson, P ;
Winblad, B ;
Blennow, K .
NEUROSCIENCE LETTERS, 1999, 273 (01) :5-8
[2]   Cerebrospinal fluid tau protein as a biochemical marker for Alzheimer's disease:: a community based follow up study [J].
Andreasen, N ;
Vanmechelen, E ;
Van de Voorde, A ;
Davidsson, P ;
Hesse, C ;
Tarvonen, S ;
Räihä, I ;
Sourander, L ;
Winblad, B ;
Blennow, K .
JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY, 1998, 64 (03) :298-305
[3]   CSF markers for Alzheimer's disease:: Total Tau, phospho-tau and Aβ42 [J].
Andreasen, N ;
Sjögren, M ;
Blennow, K .
WORLD JOURNAL OF BIOLOGICAL PSYCHIATRY, 2003, 4 (04) :147-155
[4]   Cerebrospinal fluid levels of total-tau, phospho-tau and Aβ42 predicts development of Alzheimer's disease in patients with mild cognitive impairment [J].
Andreasen, N ;
Vanmechelen, E ;
Vanderstichele, H ;
Davidsson, P ;
Blennow, K .
ACTA NEUROLOGICA SCANDINAVICA, 2003, 107 :47-51
[5]   Sensitivity, specificity, and stability of CSF-tau in AD in a community-based patient sample [J].
Andreasen, N ;
Minthon, L ;
Clarberg, A ;
Davidsson, P ;
Gottfries, J ;
Vanmechelen, E ;
Vanderstichele, H ;
Winblad, B ;
Blennow, K .
NEUROLOGY, 1999, 53 (07) :1488-1494
[6]   Cerebrospinal fluid β-amyloid(1-42) in Alzheimer disease -: Differences between early- and late-onset Alzheimer disease and stability during the course of disease [J].
Andreasen, N ;
Hesse, C ;
Davidsson, P ;
Minthon, L ;
Wallin, A ;
Winblad, B ;
Vanderstichele, H ;
Vanmechelen, E ;
Blennow, K .
ARCHIVES OF NEUROLOGY, 1999, 56 (06) :673-680
[7]   Evaluation of CSF-tau and CSF-Aβ42 as diagnostic markers for Alzheimer disease in clinical practice [J].
Andreasen, N ;
Minthon, L ;
Davidsson, P ;
Vanmechelen, E ;
Vanderstichele, H ;
Winblad, B ;
Blennow, K .
ARCHIVES OF NEUROLOGY, 2001, 58 (03) :373-379
[8]   CSF phosphorylated tau protein and mild cognitive impairment: a prospective study [J].
Arai, H ;
Ishiguro, K ;
Ohno, H ;
Moriyama, M ;
Itoh, N ;
Okamura, N ;
Matsui, T ;
Morikawa, Y ;
Horikawa, E ;
Kohno, H ;
Sasaki, H ;
Imahori, K .
EXPERIMENTAL NEUROLOGY, 2000, 166 (01) :201-203
[9]  
ARAI H, 1997, ALZHEIMERS RES, V3, P211
[10]   Synaptic pathology in Alzheimer's disease: Relation to severity of dementia, but not to senile plaques, neurofibrillary tangles, or the ApoE4 allele [J].
Blennow, K ;
Bogdanovic, N ;
Alafuzoff, I ;
Ekman, R ;
Davidsson, P .
JOURNAL OF NEURAL TRANSMISSION, 1996, 103 (05) :603-618