3.9 Article

Using subjective cognitive decline to identify high global amyloid in community-based samples: A cross-cohort study

出版社

WILEY
DOI: 10.1016/j.dadm.2019.08.004

关键词

Subjective cognitive decline; Amyloid; APOE epsilon 4; Alzheimer's disease

资金

  1. NHMRC Dementia Research Fellowship [APP1105576]
  2. Canadian Institutes of Health Research Postdoctoral Fellowship
  3. National Institutes of Health [P01 AG036694, P50 AG005134, K23 EB019023, K23 AG049087, K24 AG035007, K01 040197]
  4. Center for Functional Neuroimaging Technologies [P41EB015896]
  5. National Institute of Biomedical Imaging and Bioengineering (NIBIB)
  6. National Institutes of Health
  7. NIH [S10RR021110, S10RR023401, S10RR023043]
  8. Alzheimer's Disease Neuroimaging Initiative (ADNI) (National Institutes of Health) [U01 AG024904]
  9. DODADNI (Department of Defense) [W81XWH-12-2-0012]
  10. National Institute on Aging
  11. National Institute of Biomedical Imaging and Bioengineering
  12. AbbVie
  13. Alzheimer's Association
  14. Alzheimer's Drug Discovery Foundation
  15. Araclon Biotech
  16. BioClinica, Inc.
  17. Biogen
  18. Bristol-Myers Squibb Company
  19. CereSpir, Inc.
  20. Cogstate
  21. Eisai Inc.
  22. Elan Pharmaceuticals, Inc.
  23. Eli Lilly and Company
  24. EuroImmun
  25. F. Hoffmann-La Roche Ltd
  26. Genentech, Inc.
  27. Fujirebio
  28. GE Healthcare
  29. IXICO Ltd.
  30. Janssen Alzheimer Immunotherapy Research & Development, LLC.
  31. Johnson & Johnson Pharmaceutical Research & Development LLC.
  32. Lumosity
  33. Lundbeck
  34. Merck Co., Inc.
  35. Meso Scale Diagnostics, LLC.
  36. NeuroRx Research
  37. Neurotrack Technologies
  38. Novartis Pharmaceuticals Corporation
  39. Pfizer Inc.
  40. Piramal Imaging
  41. Servier
  42. Takeda Pharmaceutical Company
  43. Transition Therapeutics
  44. Canadian Institutes of Health Research

向作者/读者索取更多资源

Introduction: We aimed to examine the contribution of subjective cognitive decline (SCD) to reduce the number of beta-amyloid (A beta) positron emission tomography scans required for recruiting A beta+ clinically normal individuals in clinical trials. Methods: Three independent cohorts (890 clinically normal: 72 yrs 6.7; Female: 43.4%; SCD+: 24%; apolipoprotein E [APOE] epsilon 4+: 28.5%; A beta+: 32%) were used. SCD was dichotomized from one question. Using logistic regression, we classified A beta+ using the SCD dichotomy, APOE epsilon 4, sex, and age. Results: SCD increased odds of A beta+ by 1.58 relative to non-SCD. Female APOE epsilon 4 carriers with SCD exhibited higher odds of A beta+ (OR = 3.34), whereas male carriers with SCD showed a weaker, opposing effect (OR = 0.37). SCD endorsement reduces the number of A beta positron emission tomography scans to recruit A beta+ individuals by 13% and by 9% if APOE epsilon 4 status is known. Conclusion: SCD helps to classify those with high A beta, even beyond the substantial effect of APOE genotype. Collecting SCD is a feasible method for targeting recruitment for those likely on the AD trajectory. (C) 2019 The Authors. Published by Elsevier Inc. on behalf of the Alzheimer's Association.

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