4.7 Review

The Alzheimer's Disease Neuroimaging Initiative: Annual change in biomarkers and clinical outcomes

Journal

ALZHEIMERS & DEMENTIA
Volume 6, Issue 3, Pages 257-264

Publisher

ELSEVIER SCIENCE INC
DOI: 10.1016/j.jalz.2010.03.002

Keywords

Alzheimer's disease; Cerebrospinal fluid; Neuroimaging; FDG PET; MRI; Biomarkers; Clinical trial design; Mild cognitive impairment; Cognitive decline

Funding

  1. Alzheimer's Disease Neuroimaging Initiative (ADNI) (National Institutes of Health) [U01 AG024904]
  2. National Institute on Aging
  3. National Institute of Biomedical Imaging and Bioengineering
  4. Abbott
  5. AstraZeneca AB
  6. Bayer Schering Pharma AG
  7. Bristol-Myers Squibb
  8. Eisai Global Clinical Development
  9. Elan Corporation
  10. Genentech
  11. GE Healthcare
  12. GlaxoSmithKline
  13. Innogenetics
  14. Johnson and Johnson
  15. Eli Lilly and Co.
  16. Medpace, Inc
  17. Merck and Co, Inc.
  18. Novartis AG
  19. Pfizer Inc
  20. F Hoffman-La Roche
  21. Schering-Plough
  22. Synarc, Inc.
  23. Wyeth
  24. U S Food and Drug Administration
  25. NIH [P30 AG00129, K01 AG030514]
  26. Dana Foundation
  27. NATIONAL INSTITUTE ON AGING [P30AG010129, U01AG024904, K01AG030514, U19AG010483] Funding Source: NIH RePORTER

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Background: The Alzheimer's Disease Neuroimaging Initiative Phase 1 (ADNI-1) is a molt site prospective study designed to examine potential cerebrospinal fluid and imaging markers of Alzheimer's disease (AD) and their relationship to cognitive change The objective of this study was to provide a global summary of the overall results and patterns of change observed m candidate markets and clinical measures over the first 2 years of follow-up Methods: Change was summarized for 210 normal controls, 357 mild cognitive impairment. and 162 AD subjects. with baseline and at least one cognitive follow-up assessment Repeated measures and survival models were used to assess baseline biomarker levels as predictors Potential for improving clinical trials was assessed by comparison of precision of markers for capturing change in hypothetical trial designs Results: The first 12 months of complete data on ADNI participants demonstrated the potential for substantial advances in characterizing trajectories of change in a range of biomarkers and clinical outcomes, examining their relationship and timing. and assessing the potential for improvements in clinical trial design Reduced metabolism and greater brain atrophy in the mild cognitive impairment at baseline ale associated with mole rapid cognitive decline and a higher rate of conversion to AD. Use of biomarkers as study entry criteria or as outcomes could reduce the number of participants requited for clinical trials Conclusions: Analyses and comparisons of ADNI data strongly support the hypothesis that measurable change occurs in cerebiospinal fluid. position emission tomography. and magnetic resonance imaging well in advance of the actual diagnosis of AD (C) 2010 The Alzheimer's Association All rights reserved

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