4.5 Article

The National Institute on Aging-Alzheimer's Association research criteria for mild cognitive impairment due to Alzheimer's disease: predicting the outcome

出版社

SPRINGER HEIDELBERG
DOI: 10.1007/s00406-012-0349-0

关键词

Mild cognitive impairment; Alzheimer's disease; Dementia; Diagnostic criteria

资金

  1. Alzheimer's Disease Neuroimaging Initiative (ADNI) (National Institutes of Health) [U01 AG024904]
  2. NIA
  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. Alzheimer's Association
  24. Alzheimer's Drug Discovery Foundation
  25. NIH [P30AG010129, K01 AG030514]
  26. Dana Foundation

向作者/读者索取更多资源

The National Institute on Aging-Alzheimer's Association (NIA-AA) clinical research criteria for mild cognitive impairment (MCI) due to Alzheimer's disease (AD) incorporate the use of biomarkers to classify patients according to the likelihood of the presence of AD pathology. The aim of the study was to compare the risk of progression to AD dementia between the four NIA-AA MCI subgroups using data from the AD Neuroimaging Initiative. Patients with MCI were categorised according to the NIA-AA criteria into subgroups with high, intermediate, and low likelihood of the presence of AD pathology (MCI-high, MCI-intermediate, and MCI-unlikely, respectively) or into a group of patients that only met the MCI-core clinical criteria (MCI-core). Data of follow-up visits conducted 6-60 months after baseline were used to compare the relative risk of future AD dementia between the four subgroups employing a Cox regression model. The MCI-high subgroup (N = 22) had a 2.3 times higher risk of developing AD dementia compared with the MCI-core subgroup (N = 327; P = 0.002), while there was a trend for a higher risk in the MCI-high subgroup in contrast to the MCI-intermediate subgroup (N = 31, P = 0.08). No patients in the MCI-unlikely subgroup (N = 17) progressed to AD dementia. Patients with MCI-high have a higher risk for developing AD dementia. The new NIA-AA MCI criteria represent a valuable research instrument that could be incorporated into the diagnostic process of the MCI syndrome after optimisation and refinement.

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