Diagnostic value of cerebrospinal fluid Aβ ratios in preclinical Alzheimer's disease

被引:46
作者
Adamczuk, Katarzyna [1 ,2 ]
Schaeverbeke, Jolien [1 ,2 ]
Vanderstichele, Hugo M. J. [3 ]
Lilja, Johan [4 ,5 ]
Nelissen, Natalie [1 ,6 ]
Van Laere, Koen [2 ,7 ,8 ]
Dupont, Patrick [1 ,2 ]
Hilven, Kelly [9 ]
Poesen, Koen [10 ,11 ]
Vandenberghe, Rik [1 ,2 ,12 ]
机构
[1] Katholieke Univ Leuven, Lab Cognit Neurol, B-3000 Louvain, Belgium
[2] Katholieke Univ Leuven, Leuven Inst Neurosci & Dis, Alzheimer Res Ctr, B-3000 Louvain, Belgium
[3] ADx NeuroSci, B-9052 Ghent, Belgium
[4] GE Healthcare, S-75125 Uppsala, Sweden
[5] Uppsala Univ, Dept Surg Sci, Nucl Med & PET, S-75185 Uppsala, Sweden
[6] Univ Oxford, Dept Psychiat, Oxford OX3 7JX, England
[7] Katholieke Univ Leuven, Nucl Med & Mol Imaging Dept, B-3000 Louvain, Belgium
[8] Katholieke Univ Leuven Hosp, B-3000 Louvain, Belgium
[9] Katholieke Univ Leuven, Lab Neuroimmunol, B-3000 Louvain, Belgium
[10] Katholieke Univ Leuven, Lab Mol Neurobiomarker Res, B-3000 Louvain, Belgium
[11] UZ Leuven, Lab Med, B-3000 Louvain, Belgium
[12] Univ Hosp Leuven, Dept Neurol, B-3000 Louvain, Belgium
关键词
MEMORY COMPLAINTS; AMYLOID-BETA; CLINICAL-PRACTICE; DEMENTIA; F-18-FLUTEMETAMOL; CSF; VALIDATION; NEURODEGENERATION; PREVALENCE; DEPOSITION;
D O I
10.1186/s13195-015-0159-5
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Introduction: In this study of preclinical Alzheimer's disease (AD) we assessed the added diagnostic value of using cerebrospinal fluid (CSF) A beta ratios rather than A beta 42 in isolation for detecting individuals who are positive on amyloid positron emission tomography (PET). Methods: Thirty-eight community-recruited cognitively intact older adults (mean age 73, range 65-80 years) underwent F-18-flutemetamol PET and CSF measurement of A beta 1-42, A beta 1-40, A beta 1-38, and total tau (ttau). F-18-flutemetamol retention was quantified using standardized uptake value ratios in a composite cortical region (SUVRcomp) with reference to cerebellar grey matter. Based on a prior autopsy validation study, the SUVRcomp cut-off was 1.57. Sensitivities, specificities and cut-offs were defined based on receiver operating characteristic analysis with CSF analytes as variables of interest and F-18-flutemetamol positivity as the classifier. We also determined sensitivities and CSF cut-off values at fixed specificities of 90 % and 95 %. Results: Seven out of 38 subjects (18 %) were positive on amyloid PET. A beta 42/ttau, A beta 42/A beta 40, A beta 42/A beta 38, and A beta 42 had the highest accuracy to identify amyloid-positive subjects (area under the curve (AUC) >= 0.908). A beta 40 and A beta 38 had significantly lower discriminative power (AUC = 0.571). When specificity was fixed at 90 % and 95 %, A beta 42/ttau had the highest sensitivity among the different CSF markers (85.71 % and 71.43 %, respectively). Sensitivity of A beta 42 alone was significantly lower under these conditions (57.14 % and 42.86 %, respectively). Conclusion: For the CSF-based definition of preclinical AD, if a high specificity is required, our data support the use of A beta 42/ttau rather than using A beta 42 in isolation.
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