Cited by 58Dementia and Cognitive Impairment ResearchAlzheimer's disease research and treatmentsCancer-related cognitive impairment studies

Comparative analytical performance of multiple plasma Aβ42 and Aβ40 assays and their ability to predict positron emission tomography amyloid positivity

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Zicha, Stephen, Bateman, Randall J., Shaw, Leslie M., Zetterberg, Henrik, Bannon, Anthony W., Horton, Wesley A., Baratta, Mike, Kolb, Hartmuth C. +18 more·2023·Alzheimer's & Dementia

Abstract

Introduction: This report details the approach taken to providing a dataset allowing for analyses on the performance of recently developed assays of amyloid beta (Aβ) peptides in plasma and the extent to which they improve the prediction of amyloid positivity. Methods: Alzheimer's Disease Neuroimaging Initiative plasma samples with corresponding amyloid positron emission tomography (PET) data were run on six plasma Aβ assays. Statistical tests were performed to determine whether the plasma Aβ measures significantly improved the area under the receiver operating characteristic curve for predicting amyloid PET status compared to age and apolipoprotein E ( APOE ) genotype. Results: The age and APOE genotype model predicted amyloid status with an area under the curve (AUC) of 0.75. Three assays improved AUCs to 0.81, 0.81, and 0.84 ( P < .05, uncorrected for multiple comparisons). Discussion: Measurement of Aβ in plasma contributes to addressing the amyloid component of the ATN (amyloid/tau/neurodegeneration) framework and could be a first step before or in place of a PET or cerebrospinal fluid screening study. Highlights: The Foundation of the National Institutes of Health Biomarkers Consortium evaluated six plasma amyloid beta (Aβ) assays using Alzheimer's Disease Neuroimaging Initiative samples. Three assays improved prediction of amyloid status over age and apolipoprotein E ( APOE ) genotype. Plasma Aβ42/40 predicted amyloid positron emission tomography status better than Aβ42 or Aβ40 alone.

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References 24 · Cited by 58

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Authors
Zicha, S., Bateman, R. J., Shaw, L. M., Zetterberg, H., Bannon, A. W., Horton, W. A., Baratta, M., Kolb, H. C., Dobler, I., Mordashova, Y., Saad, Z. S., Raunig, D. L., Spanakis, E. (., Li, Y., Schindler, S. E., Ferber, K., Rubel, C. E., Martone, R. L., Weber, C. J., Edelmayer, R. M., Meyers, E. A., Bollinger, J. G., Rosenbaugh, E. G., Potter, W. Z., (ADNI), A. D. N. I., & Foundation for the National Institutes of Health (FNIH) Biomarkers Consortium Plasma Aβ as a Predictor of Amyloid Positivity in Alzheimer's Disease Project Team
Affiliations
  • Takeda Pharmaceutical Company Ltd. Cambridge Massachusetts USA
  • Washington University in St. Louis (US)
  • University of Pennsylvania (US)
  • Sahlgrenska University Hospital (SE)
  • AbbVie (United States) (US)
  • Foundation for the National Institutes of Health (US)
  • Neuroscience Biomarkers Janssen Research and Development LLC La Jolla California USA
  • AbbVie (Germany) (DE)
  • Biogen (United States) (US)
  • Alzheimer's Association (US)
  • Highly qualified expert
Corresponding author
Zicha, Stephen
Venue
Alzheimer's & Dementia
Publisher
Wiley
Published
2022-07-12
Volume
19
Issue
3
Pages
956-966
ISSN
  • 1552-5260 (ISSN-L)
  • 1552-5279
OpenAlex
W4285088596
Cited by
58
References
24
Citations by year
2026: 6 · 2025: 15 · 2024: 19 · 2023: 13 · 2022: 4 · 2021: 1
FWCI
8.31
Type
journal article
Language
en
Open access
Locations
  • Alzheimer s & Dementia (publishedVersion, cc-by-nc)
  • PubMed (publishedVersion)
  • PubMed Central (acceptedVersion, other-oa)
  • UCL Discovery (University College London) (submittedVersion)
Funders
  • U.S. Department of Defense (W81XWH, W81XWH-12-2-, W81XWH1220012, AG024904)
  • Foundation for the National Institutes of Health (W81XWH-12-2-0012, U19 AG024904, AG024904)
  • Alzheimer's Association (W81XWH-12-2-0012)
  • Bristol-Myers Squibb (AG024904, W81XWH-12-2-0012)
  • Eli Lilly and Company (AG024904, W81XWH-12-2-0012)
  • Pfizer (AG024904, W81XWH-12-2-0012)
  • Biogen (W81XWH-12-2-0012, AG024904)
  • University of Southern California (W81XWH-12-2-0012)
  • AbbVie (W81XWH-12-2-0012, AG024904)
  • University of Pennsylvania
  • Meso Scale Diagnostics (AG024904, W81XWH-12-2-0012)
  • Alzheimer's Disease Neuroimaging Initiative (W81XWH-12-2–0012, AG024904, W81XWH-12-2-, U19 AG024904)
  • BioClinica (W81XWH-12-2-0012, AG024904)
  • Novartis Pharmaceuticals Corporation (W81XWH-12-2-0012, AG024904)
  • Northern California Institute for Research and Education (W81XWH-12-2-0012)
  • Eisai (W81XWH-12-2-0012, AG024904)
  • Göteborgs Universitet
  • Servier (AG024904, W81XWH-12-2-0012)
  • H. Lundbeck A/S (AG024904, W81XWH-12-2-0012)
  • IXICO (AG024904, W81XWH-12-2-0012)
  • National Institutes of Health (5u01ag024904-10, W81XWH, W81XWH-12-2-0012, AG024904)
  • Genentech (W81XWH-12-2-0012, AG024904)
  • Canadian Institutes of Health Research (W81XWH-12-2-0012)
  • National Institute on Aging (U01-AG-024904, W81XWH-12-2–0012, AG 024904, P30AG010124, R56AG061900, RF1AG061900, U19AG024904, P30AG072979)
Topics
  • Health Sciences › Medicine › Psychiatry and Mental health › Dementia and Cognitive Impairment Research
  • Health Sciences › Medicine › Physiology › Alzheimer's disease research and treatments
  • Health Sciences › Medicine › Pulmonary and Respiratory Medicine › Cancer-related cognitive impairment studies
Keywords
plasma amyloid-beta, amyloid-beta 42
MeSH terms
Aged, Aged, 80 and over, Alzheimer Disease, Apolipoproteins E, Female, Genotype, Humans, Male, Peptide Fragments, Biomarkers, Amyloid beta-Peptides, Positron-Emission Tomography

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