4.7 Article

Indicators of amyloid burden in a population-based study of cognitively normal elderly

Journal

NEUROLOGY
Volume 79, Issue 15, Pages 1570-1577

Publisher

LIPPINCOTT WILLIAMS & WILKINS
DOI: 10.1212/WNL.0b013e31826e2696

Keywords

-

Funding

  1. NIH [P50 AG016574, U01 AG006786, U01 AG037526, K01 MH068351, RO1 AG011378, K01 AG028573]
  2. NIH/NIA
  3. Baxter
  4. Elan Pharmaceuticals
  5. Forest Pharmaceuticals
  6. NIH
  7. GE Healthcare
  8. Siemens Molecular Imaging
  9. NIH (NIA, NCI)
  10. MN Partnership for Biotechnology and Medical Genomics
  11. Leukemia & Lymphoma Society
  12. Abbott Research Labs
  13. Robert Wood Johnson Foundation
  14. European Union Regional Development Fund
  15. Cephalon, Inc.
  16. Alzheimer's Association
  17. Center for Inherited Disease Research
  18. Baxter International Inc.
  19. Allon Therapeutics, Inc.
  20. Alexander Family Alzheimer's Disease Research Professorship of the Mayo Foundation
  21. Alexander Family Alzheimer's Disease Research Professorship, GE Healthcare [R01 AG034676]

Ask authors/readers for more resources

Objectives: Secondary prevention trials in subjects with preclinical Alzheimer disease may require documentation of brain amyloidosis. The identification of inexpensive and noninvasive screening variables that can identify individuals who have significant amyloid accumulation would reduce screening costs. Methods: A total of 483 cognitively normal (CN) individuals, aged 70-92 years, from the population-based Mayo Clinic Study of Aging, underwent Pittsburgh compound B (PiB)-PET imaging. Logistic regression determined whether age, sex, APOE genotype, family history, or cognitive performance was associated with odds of a PiB retention ratio >1.4 and >1.5. Area under the receiver operating characteristic curve (AUROC) evaluated the discrimination between PiB-positive and -negative subjects. For each characteristic, we determined the number needed to screen in each age group (70-79 and 80-89) to identify 100 participants with PiB > 1.4 or >1.5. Results: A total of 211 (44%) individuals had PiB >1.4 and 151 (31%) >1.5. In univariate and multivariate models, discrimination was modest (AUROC similar to 0.6-0.7). Multivariately, age and APOE best predicted odds of PiB > 1.4 and >1.5. Subjective memory complaints were similar to cognitive test performance in predicting PiB >1.5. Indicators of PiB positivity varied with age. Screening APOE epsilon 4 carriers alone reduced the number needed to screen to enroll 100 subjects with PIB >1.5 by 48% in persons aged 70-79 and 33% in those aged 80-89. Conclusions: Age and APOE genotype are useful predictors of the likelihood of significant amyloid accumulation, but discrimination is modest. Nonetheless, these results suggest that inexpensive and noninvasive measures could significantly reduce the number of CN individuals needed to screen to enroll a given number of amyloid-positive subjects. Neurology (R) 2012; 79: 1570-1577

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.7
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available