TY - JOUR
T1 - Cerebrospinal fluid biomarkers measured by Elecsys assays compared to amyloid imaging
AU - Schindler, Suzanne E.
AU - Gray, Julia D.
AU - Gordon, Brian A.
AU - Xiong, Chengjie
AU - Batrla-Utermann, Richard
AU - Quan, Marian
AU - Wahl, Simone
AU - Benzinger, Tammie L.S.
AU - Holtzman, David M.
AU - Morris, John C.
AU - Fagan, Anne M.
N1 - Publisher Copyright:
© 2018 The Authors
PY - 2018/11
Y1 - 2018/11
N2 - Introduction: Levels of amyloid β peptide 42 (Aβ42), total tau, and phosphorylated tau-181 are well-established cerebrospinal fluid (CSF) biomarkers of Alzheimer's disease, but variability in manual plate-based assays has limited their use. We examined the relationship between CSF biomarkers, as measured by a novel automated immunoassay platform, and amyloid positron emission tomography. Methods: CSF samples from 200 individuals underwent separate analysis for Aβ42, total tau, and phosphorylated tau-181 with automated Roche Elecsys assays. Aβ40 was measured with a commercial plate-based assay. Positron emission tomography with Pittsburgh Compound B was performed less than 1 year from CSF collection. Results: Ratios of CSF biomarkers (total tau/Aβ42, phosphorylated tau-181/Aβ42, and Aβ42/Aβ40) best discriminated Pittsburgh Compound B–positive from Pittsburgh Compound B–negative individuals. Discussion: CSF biomarkers and amyloid positron emission tomography reflect different aspects of Alzheimer's disease brain pathology, and therefore, less-than-perfect correspondence is expected. Automated assays are likely to increase the utility of CSF biomarkers.
AB - Introduction: Levels of amyloid β peptide 42 (Aβ42), total tau, and phosphorylated tau-181 are well-established cerebrospinal fluid (CSF) biomarkers of Alzheimer's disease, but variability in manual plate-based assays has limited their use. We examined the relationship between CSF biomarkers, as measured by a novel automated immunoassay platform, and amyloid positron emission tomography. Methods: CSF samples from 200 individuals underwent separate analysis for Aβ42, total tau, and phosphorylated tau-181 with automated Roche Elecsys assays. Aβ40 was measured with a commercial plate-based assay. Positron emission tomography with Pittsburgh Compound B was performed less than 1 year from CSF collection. Results: Ratios of CSF biomarkers (total tau/Aβ42, phosphorylated tau-181/Aβ42, and Aβ42/Aβ40) best discriminated Pittsburgh Compound B–positive from Pittsburgh Compound B–negative individuals. Discussion: CSF biomarkers and amyloid positron emission tomography reflect different aspects of Alzheimer's disease brain pathology, and therefore, less-than-perfect correspondence is expected. Automated assays are likely to increase the utility of CSF biomarkers.
KW - Alzheimer's disease
KW - Amyloid
KW - Biomarker
KW - Cerebrospinal fluid
KW - Cutoff
UR - http://www.scopus.com/inward/record.url?scp=85044286063&partnerID=8YFLogxK
U2 - 10.1016/j.jalz.2018.01.013
DO - 10.1016/j.jalz.2018.01.013
M3 - Article
C2 - 29501462
AN - SCOPUS:85044286063
SN - 1552-5260
VL - 14
SP - 1460
EP - 1469
JO - Alzheimer's and Dementia
JF - Alzheimer's and Dementia
IS - 11
ER -