4.6 Article

Adding Recognition Discriminability Index to the Delayed Recall Is Useful to Predict Conversion from Mild Cognitive Impairment to Alzheimer's Disease in the Alzheimer's Disease Neuroimaging Initiative

Journal

FRONTIERS IN AGING NEUROSCIENCE
Volume 9, Issue -, Pages -

Publisher

FRONTIERS MEDIA SA
DOI: 10.3389/fnagi.2017.00046

Keywords

disease progression; memory; recognition discriminability; mild cognitive impairment; Alzheimer's disease; signal detection theory

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, the National Institute of Biomedical Imaging and Bioengineering
  4. Alzheimer's Association
  5. Alzheimer's Drug Discovery Foundation
  6. BioClinica, Inc.
  7. Biogen Idec Inc.
  8. Bristol-Myers Squibb Company
  9. Eisai Inc.
  10. Elan Pharmaceuticals, Inc.
  11. Eli Lilly and Company
  12. F. Hoffmann-La Roche Ltd
  13. Genentech, Inc.
  14. GE Healthcare
  15. Innogenetics, N.V.
  16. IXICO Ltd.
  17. Janssen Alzheimer Immunotherapy Research & Development, LLC.
  18. Johnson & Johnson Pharmaceutical Research & Development LLC.
  19. Medpace, Inc.
  20. Merck Co., Inc.
  21. Meso Scale Diagnostics, LLC.
  22. NeuroRx Research
  23. Novartis Pharmaceuticals Corporation
  24. Pfizer Inc.
  25. Piramal Imaging
  26. Servier
  27. Synarc Inc.
  28. Takeda Pharmaceutical Company
  29. Canadian Institutes of Health Research

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Background : Ongoing research is focusing on the identification of those individuals with mild cognitive impairment (MCI) who are most likely to convert to Alzheimer's disease (AD). We investigated whether recognition memory tasks in combination with delayed recall measure of episodic memory and CSF biomarkers can predict MCI to AD conversion at 24-month follow-up. Methods : A total of 397 amnestic-MCI subjects from Alzheimer's disease Neuroimaging Initiative were included. Logistic regression modeling was done to assess the predictive value of all RAVLT measures, risk factors such as age, sex, education, APOE genotype, and CSF biomarkers for progression to AD. Estimating adjusted odds ratios was used to determine which variables would produce an optimal predictive model, and whether adding tests of interaction between the RAVLT Delayed Recall and recognition measures (traditional score and d-prime) would improve prediction of the conversion from a-MCI to AD. Results : 112 (28.2%) subjects developed dementia and 285 (71.8%) subjects did not. Of the all included variables, CSF A beta 1-42 levels, RAVLT Delayed Recall, and the combination of RAVLT Delayed Recall and d-prime were predictive of progression to AD ( chi(2) = 38.23, df = 14, p < 0.001). Conclusions : The combination of RAVLT Delayed Recall and d-prime measures may be predictor of conversion from MCI to AD in the ADNI cohort, especially in combination with amyloid biomarkers. A predictive model to help identify individuals at-risk for dementia should include not only traditional episodic memory measures (delayed recall or recognition), but also additional variables (d-prime) that allow the homogenization of the assessment procedures in the diagnosis of MCI.

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