Cerebrospinal Fluid Biomarkers in Cerebral Amyloid Angiopathy: New Data and Quantitative Meta-Analysis

被引:18
作者
Margraf, Nils G. [1 ]
Jensen-Kondering, Ulf [2 ,3 ]
Weiler, Caroline [1 ]
Leypoldt, Frank [1 ,4 ]
Maetzler, Walter [1 ]
Philippen, Sarah [1 ]
Bartsch, Thorsten [1 ]
Flueh, Charlotte [5 ]
Roecken, Christoph [6 ]
Moeller, Bettina [1 ]
Royl, Georg [7 ]
Neumann, Alexander [3 ]
Brueggemann, Norbert [7 ,8 ]
Roeben, Benjamin [9 ,10 ]
Schulte, Claudia [9 ,10 ]
Bender, Benjamin [11 ]
Berg, Daniela [1 ,9 ]
Kuhlenbaeumer, Gregor [1 ]
机构
[1] Univ Kiel, Univ Med Ctr Schleswig Holstein, Dept Neurol, Campus Kiel, Kiel, Germany
[2] Univ Kiel, Univ Med Ctr Schleswig Holstein, Dept Radiol & Neuroradiol, Campus Kiel, Kiel, Germany
[3] Univ Med Ctr Schleswig Holstein, Dept Neuroradiol, Campus Lubeck, Lubeck, Germany
[4] Univ Med Ctr Schleswig Holstein, Inst Clin Chem, Kiel, Germany
[5] Univ Kiel, Univ Med Ctr Schleswig Holstein, Dept Neurosurg, Campus Kiel, Kiel, Germany
[6] Univ Kiel, Univ Med Ctr Schleswig Holstein, Dept Pathol, Campus Kiel, Kiel, Germany
[7] Univ Med Ctr Schleswig Holstein, Dept Neurol, Campus Lubeck, Lubeck, Germany
[8] Univ Lubeck, Inst Neurogenet, Lubeck, Germany
[9] Univ Tubingen, Hertie Inst Clin Brain Res, Dept Neurodegenerat, Tubingen, Germany
[10] Univ Tubingen, German Ctr Neurodegenerat Dis, Tubingen, Germany
[11] Univ Tubingen Hosp, Dept Neuroradiol Diagnost & Intervent Neuroradiol, Tubingen, Germany
来源
FRONTIERS IN AGING NEUROSCIENCE | 2022年 / 14卷
关键词
cerebral amyloid angiopathy (CAA); cerebrospinal fluid (CSF); high-precision electro-chemiluminescence immunoassay (ECLIA); Boston criteria; Alzheimer's dementia (AD); SMALL-VESSEL DISEASE; ALZHEIMER-DISEASE; A-BETA(42)/A-BETA(40); DIAGNOSIS; DEMENTIA; PET;
D O I
10.3389/fnagi.2022.783996
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
BackgroundTo evaluate the diagnostic accuracy of cerebrospinal fluid (CSF) biomarkers in patients with probable cerebral amyloid angiopathy (CAA) according to the modified Boston criteria in a retrospective multicentric cohort. MethodsBeta-amyloid 1-40 (A beta 40), beta-amyloid 1-42 (A beta 42), total tau (t-tau), and phosphorylated tau 181 (p-tau(181)) were measured in 31 patients with probable CAA, 28 patients with Alzheimer's disease (AD), and 30 controls. Receiver-operating characteristics (ROC) analyses were performed for the measured parameters as well as the A beta 42/40 ratio to estimate diagnostic parameters. A meta-analysis of all amenable published studies was conducted. ResultsIn our data A beta 42/40 (AUC 0.88) discriminated best between CAA and controls while A beta 40 did not perform well (AUC 0.63). Differentiating between CAA and AD, p-tau(181) (AUC 0.75) discriminated best in this study while A beta 40 (AUC 0.58) and A beta 42 (AUC 0.54) provided no discrimination. In the meta-analysis, A beta 42/40 (AUC 0.90) showed the best discrimination between CAA and controls followed by t-tau (AUC 0.79), A beta 40 (AUC 0.76), and p-tau(181) (AUC 0.71). P-tau(181) (AUC 0.76), A beta 40 (AUC 0.73), and t-tau (AUC 0.71) differentiated comparably between AD and CAA while A beta 42 (AUC 0.54) did not. In agreement with studies examining AD biomarkers, A beta 42/40 discriminated excellently between AD and controls (AUC 0.92-0.96) in this study as well as the meta-analysis. ConclusionThe analyzed parameters differentiate between controls and CAA with clinically useful accuracy (AUC > similar to 0.85) but not between CAA and AD. Since there is a neuropathological, clinical and diagnostic continuum between CAA and AD, other diagnostic markers, e.g., novel CSF biomarkers or other parameters might be more successful.
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页数:11
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