4.7 Article

Limited agreement between biomarkers of neuronal injury at different stages of Alzheimer's disease

Journal

ALZHEIMERS & DEMENTIA
Volume 10, Issue 6, Pages 684-689

Publisher

ELSEVIER SCIENCE INC
DOI: 10.1016/j.jalz.2014.03.006

Keywords

Dementia; Agreement; Diagnostic criteria; Tau; FDG-PET; Hippocampal atrophy

Funding

  1. Alzheimer's Disease Neuroimaging Initiative (ADNI) (National Institutes of Health Grant) [U01 AG024904]
  2. DOD ADNI (Department of Defense) [W81XWH-12-2-0012]
  3. National Institute on Aging
  4. National Institute of Biomedical Imaging and Bioengineering
  5. Canadian Institutes of Health Research
  6. Alzheimer's Association
  7. Alzheimer Drug Discovery Foundation
  8. BioClinica, Inc
  9. Biogen Idec
  10. Bristol-Myers Squibb
  11. Eisai Inc
  12. Elan Pharmaceuticals, Inc
  13. Eli Lilly
  14. F. Hoffmann-La Roche Ltd
  15. Genentech
  16. GE
  17. Innogenetics
  18. N.V.
  19. IXICO Ltd
  20. Janssen Alzheimer Immunotherapy Research & Development, LLC
  21. Johnson & Johnson Pharmaceutical Research & Development, LLC
  22. Medpace, Inc
  23. Merck Co., Inc.
  24. Meso Scale Diagnostics, LLC
  25. NeuroRx Research
  26. Novartis
  27. Pfizer
  28. Piramal Imaging
  29. Servier
  30. Synarc Inc
  31. Takeda Pharmaceutical Company

Ask authors/readers for more resources

New diagnostic criteria for Alzheimer's disease (AD) treat different biomarkers of neuronal injury as equivalent. Here, we quantified the degree of agreement between hippocampal volume on structural magnetic resonance imaging, regional glucose metabolism on positron emission tomography, and levels of phosphorylated tau in cerebrospinal fluid (CSF) in 585 subjects from all phases of the AD Neuroimaging Initiative. The overall chance-corrected agreement was poor (Cohen kappa, 0.24-0.34), in accord with a high rate of conflicting findings (26%-41%). Neither diagnosis nor APOE epsilon 4 status significantly influenced the distribution of agreement between the biomarkers. The degree of agreement tended to be higher in individuals with abnormal versus normal CSF beta-am-yloid (A beta(1-42)) levels. Prospective diagnostic criteria for AD should address the relative importance of markers of neuronal injury and elaborate a way of dealing with conflicting biomarker findings. (C) 2014 The Alzheimer's Association. All rights reserved.

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