Prediction of Alzheimer's disease using the CSF Aβ42/Aβ40 ratio in patients with mild cognitive impairment

被引:237
作者
Hansson, Oskar
Zetterberg, Henrik
Buchhave, Peder
Andreasson, Ulf
Londos, Elisabet
Minthon, Lennart
Blennow, Kaj
机构
[1] Lund Univ, Dept Clin Sci Malmo, Clin Memory Res Unit, Malmo, Sweden
[2] Malmo Univ Hosp, Neuropsychiat Clin, Malmo, Sweden
[3] Univ Gothenburg, Sahlgrenska Univ Hosp, Dept Psychiat & Neurochem, Inst Neurosci & Physiol, Gothenburg, Sweden
[4] Univ Gothenburg, Sahlgrenska Univ Hosp, Inst Biomed, Dept Clin Chem & Transfus Med, Gothenburg, Sweden
关键词
biomarkers; cerebrospinal fluid; amyloid; mild cognitive impairment; Alzheimer's disease;
D O I
10.1159/000100926
中图分类号
R592 [老年病学]; C [社会科学总论];
学科分类号
03 ; 0303 ; 100203 ;
摘要
Evidence supports an important role for beta-amyloid (A beta) in the pathogenesis of Alzheimer's disease ( AD). Here, we investigate baseline levels of the 40- and 42-amino-acid-long A beta peptides (A beta 40 and A beta 42) in cerebrospinal fluid (CSF) from a cohort of patients with mild cognitive impairment (MCI, n = 137) in relation to the final diagnosis after 4 - 6 years of follow-up time. CSF A beta 42 concentration at baseline and the A beta 42/A beta 40 ratio were significantly decreased in the MCI patients who developed AD as compared to cognitively stable MCI patients and MCI patients who developed other forms of dementia ( p < 0.001). The baseline levels of A beta 40 were similar in all MCI groups but correlated with change in Mini Mental State Examination scores in converters to AD. The A beta 42/A beta 40 ratio was superior to A beta 42 concentration with regard to identifying incipient AD in MCI ( p < 0.05). In conclusion, the data provide further support for the view that amyloid precursor protein metabolism is disturbed in early sporadic AD and points to the usefulness of the A beta 42/ A beta 40 ratio as a predictive biomarker for AD. Copyright (C) 2007 S. Karger AG, Basel.
引用
收藏
页码:316 / 320
页数:5
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