Blood-Cerebrospinal Fluid Barrier Permeability in Alzheimer's Disease

被引:62
作者
Chalbot, Sonia
Zetterberg, Henrik [2 ]
Blennow, Kaj [2 ]
Fladby, Tormod [3 ,4 ]
Andreasen, Niels [5 ]
Grundke-Iqbal, Inge
Iqbal, Khalid [1 ]
机构
[1] New York State Inst Basic Res Dev Disabil, Dept Neurochem, Staten Isl, NY 10314 USA
[2] Sahlgrens Univ Hosp, Clin Neurochem Lab, Molndal, Sweden
[3] Akershus Univ Hosp, Dept Neurol, Lorenskog, Norway
[4] Univ Oslo, Fac Div, Akershus Univ Hosp, Dept Neurol, Oslo, Norway
[5] Karolinska Inst, Dept Geriatr Med, Karolinska Univ Hosp, Alzheimer Dis Res Ctr,Dept NVS,Memory Clin, S-10401 Stockholm, Sweden
基金
瑞典研究理事会; 美国国家卫生研究院;
关键词
Albumin; Alzheimer's disease; cerebrospinal fluid; secretory phospholipase A2; CENTRAL-NERVOUS-SYSTEM; CONTRAST-ENHANCED MRI; WHITE-MATTER LESIONS; BRAIN-BARRIER; CEREBROVASCULAR PATHOLOGY; PHOSPHOLIPASE-A2; ACTIVITY; MULTIPLE-SCLEROSIS; VASCULAR DEMENTIA; MAJOR DEPRESSION; REFERENCE VALUES;
D O I
10.3233/JAD-2011-101959
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The role of blood-cerebrospinal fluid barrier (BCB) dysfunction in Alzheimer's disease (AD) has been addressed but not yet established. We evaluated the BCB integrity in 179 samples of cerebrospinal fluid (CSF) retrospectively collected from AD patients and control cases using both CSF/serum albumin ratio (Q(Alb)) and CSF secretory Ca(2+)-dependent phospholipase A2 (sPLA2) activity. These analyses were supplemented with the measurement of total tau, amyloid-beta(1-42) (A beta(1-42)), and ubiquitin CSF levels. We found that due to its higher sensitivity, CSF sPLA2 activity could 1) discriminate AD from healthy controls and 2) showed BCB impairment in neurological control cases while QAlb could not. Moreover, the CSF sPLA2 activity measurement showed that around half of the AD patients were characterized by a BCB impairment. The BCB dysfunction observed in AD was independent from Mini-Mental State Examination score as well as CSF levels of total tau, A beta(1-42), and ubiquitin. Finally, the BCB dysfunction was not limited to any of the CSF biomarkers-based previously identified subgroups of AD. These results suggest that the BCB damage occurs independent of and probably precedes both A beta and tau pathologies in a restricted subgroup of AD patients.
引用
收藏
页码:505 / 515
页数:11
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