Concordance of CSF measures of Alzheimer's pathology with amyloid PET status in a preclinical cohort: A comparison of Lumipulse and established immunoassays

被引:8
|
作者
Keshavan, Ashvini [1 ]
Wellington, Henrietta [2 ]
Chen, Zhongbo [1 ]
Khatun, Ayesha [1 ]
Chapman, Miles [3 ]
Hart, Melanie [3 ,4 ]
Cash, David M. [1 ]
Coath, William [1 ]
Parker, Thomas D. [1 ]
Buchanan, Sarah M. [1 ]
Keuss, Sarah E. [1 ]
Harris, Matthew J. [1 ]
Murray-Smith, Heidi [1 ]
Heslegrave, Amanda [2 ]
Fox, Nick C. [1 ]
Zetterberg, Henrik [2 ,5 ]
Schott, Jonathan M. [1 ]
机构
[1] UCL, Dementia Res Ctr, UCL Queen Sq Inst Neurol, London, England
[2] UCL, UK DRI, Fluid Biomarkers Lab, UK Dementia Res Inst, London, England
[3] Natl Hosp Neurol & Neurosurg, Neuroimmunol & CSF Lab, London, England
[4] UCL, Dept Neuroinflammat, UCL Queen Sq Inst Neurol, London, England
[5] Univ Gothenburg, Sahlgrenska Univ Hosp, Sahlgrenska Acad, Clin Neurochem Lab,Dept Psychiat & Neurochem,Inst, Molndal, Sweden
基金
英国医学研究理事会;
关键词
amyloid; CSF; Lumipulse; PET; tau; BIRTH COHORT; DEMENTIA; NEUROPATHOLOGY; VALIDATION; A-BETA(42); CRITERIA; DISEASE; RATIO;
D O I
10.1002/dad2.12097
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Introduction: We assessed the concordance of cerebrospinal fluid (CSF) amyloid beta (A beta) and tau measured on the fully automated Lumipulse platform with pre-symptomatic Alzheimer's disease (AD) pathology on amyloid positron emission tomography (PET). Methods: In 72 individuals from the Insight 46 study, CSF A beta 40, A beta 42, total tau (t-tau), and phosphorylated tau at site 181 (p-tau181) were measured using Lumipulse, INNOTEST, and Meso Scale Discovery (MSD) assays, and inter-platform Pearson correlations were derived. Logistic regressions and receiver-operating characteristic analysis generated CSF cut-points optimizing concordance with F-18-florbetapir amyloid PET status (n = 63). Results: Measurements of CSF A beta, p-tau181, and their ratios correlated well across platforms (r 0.84-.94, P < .0001); those of t-tau and t-tau/A beta 42 correlated moderately (r 0.57-0.79, P < .0001). The best concordance with amyloid PET (100% sensitivity and 94% specificity) was afforded by cut-points of 0.110 for Lumipulse A beta 42/A beta 40, 0.087 for MSD A beta 42/A beta 40, and 25.3 for Lumipulse A beta 42/p-tau181. Discussion: The Lumipulse platform provides comparable sensitivity and specificity to established CSF immunoassays in identifying pre-symptomatic AD pathology.
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页数:10
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