Using Cerebrospinal Fluid Marker Profiles in Clinical Diagnosis of Dementia with Lewy Bodies, Parkinson's Disease, and Alzheimer's Disease

被引:39
作者
Kaerst, Lisa [1 ]
Kuhlmann, Andre [1 ]
Wedekind, Dirk [2 ]
Stoeck, Katharina [1 ]
Lange, Peter [1 ]
Zerr, Inga [1 ]
机构
[1] Univ Gottingen, Univ Med Ctr, Clin Dementia Ctr, Dept Neurol, D-37075 Gottingen, Germany
[2] Univ Gottingen, Univ Med Ctr, Clin Dementia Ctr, Dept Psychiat, D-37075 Gottingen, Germany
关键词
Alzheimer's disease; amyloid-beta; cerebrospinal fluid; clinical diagnosis; dementia; dementia with Lewy bodies; Parkinson's disease; tau; AMYLOID-BETA-PEPTIDES; PHOSPHORYLATED TAU; CSF BIOMARKERS; BODY DISEASE; PROTEIN; BETA-AMYLOID(1-42); CRITERIA;
D O I
10.3233/JAD-130995
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Background: Dementia with Lewy bodies (DLB) is difficult to differentiate from other neuro-degenerative diseases. Patients are often mistaken to suffer from Parkinson's disease (PD) or Alzheimer's disease (AD) because of the overlapping clinical appearances concerning cognition and movement. Objective: We investigated the possibility for a valid differential diagnosis using cerebrospinal fluid (CSF) biomarkers. Methods: In the context of a large retrospective study, we analyzed data of patients suffering from degenerative, ischemic, or inflammatory CNS (central nervous system) diseases and identified those with DLB (n = 34), PD (n = 37), and AD (n = 47) for further analyses. Results: We detected abnormalities in the CSF profiles of those patients with DLB while using a combination of decreased amyloid-alpha(A beta) 42 and increased tau levels. By stratification of data by disease severity, we observed a high sensitivity of this combination especially in the subgroup of patients with advanced stages, while the sensitivity in early forms was lower. In addition, with clinical deterioration, the abnormalities in the CSF profile became more pronounced. Conclusion: We conclude that DLB can be distinguished from PD, in spite of both being synucleinopathies, by CSF profiles using neurodegenerative marker analysis. The pathophysiology of increased tau and decreased A beta levels in those conditions has to be elucidated further, since both proteins are known to be involved in the pathogenesis of AD, but no clear explanation has been postulated for DLB yet.
引用
收藏
页码:63 / 73
页数:11
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