Combination assay of CSF Tau, Aβ1-40 and Aβ1-42(43) as a biochemical marker of Alzheimer's disease

被引:192
作者
Shoji, M
Matsubara, E
Kanai, M
Watanabe, M
Nakamura, T
Tomidokoro, Y
Shizuka, M
Wakabayashi, K
Igeta, Y
Ikeda, Y
Mizushima, K
Amari, M
Ishiguro, K
Kawarabayashi, T
Harigaya, Y
Okamoto, K
Hirai, S
机构
[1] Gunma Univ, Sch Med, Dept Neurol, Maebashi, Gumma 371, Japan
[2] Gunma Univ, Sch Med, Biosignal Res Ctr, Maebashi, Gumma 371, Japan
[3] Geriatr Res Inst & Hosp, Maebashi, Gumma 371, Japan
[4] Tokyo Metropolitan Neurol Hosp, Fuchu, Tokyo 183, Japan
关键词
CSF; Tau; A beta 1-40; A beta 1-42; Alzheimer's disease;
D O I
10.1016/S0022-510X(98)00122-1
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Cerebrospinal fluid samples from a total of 157 subjects consisting of 55 patients with sporadic Alzheimer's disease (AD), 34 normal controls, 23 patients with non-AD dementia, and 45 with other neurological diseases were examined by ELISA of tau, A beta 1-40, and A beta 1-42(43). The AD group had a significantly higher level of tau than the normal control group (P<0.001), and the diagnostic sensitivity was 31% and specificity was 94%. CSF A beta 1-40 levels did not show any significant differences. Although the level of A beta 1-42(43) was decreased significantly in the AD group compared to the control group (P<0.005), the overlap of A beta 1-42(43) levels among all groups meant that none of the AD samples exceeded the cut-off value, the mean 2SD of normal control subjects. Reduction of A beta 1-42(43) levels in AD resulted in a significant increase in the ratio of A beta 1-40 to A beta 1-42(43) (A beta ratio) as an improved marker. The diagnostic sensitivity and specificity of A beta ratio were 51% and 82% respectively. The three indexes, using the tan level and A beta ratio (tau or A beta ratio, deviation score and tau x A beta ratio), showed better sensitivity (58%, 67%, 69%) and specificity (82%, 86%, 88%) than previously reported methods. Combination assay for CSF tau, A beta 1-40 and A beta 1-42(43) in CSF is a biological marker of AD and may be useful to biochemically monitor subjects under treatment. (C) 1998 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:134 / 140
页数:7
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