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Applications of amyloid, tau, and neuroinflammation PET imaging to Alzheimer's disease and mild cognitive impairment

期刊

HUMAN BRAIN MAPPING
卷 40, 期 18, 页码 5424-5442

出版社

WILEY
DOI: 10.1002/hbm.24782

关键词

Alzheimer's disease; amyloid; mild cognitive impairment; neuroinflammation; neuropathology; PET; tau

资金

  1. Alzheimer's Disease Neuroimaging Initiative
  2. European Commission IMI2 fund
  3. Alzheimer's Research UK
  4. National Institute for Health Research
  5. AVID Radiopharmaceuticals
  6. Medical Research Council
  7. Curium
  8. Invicro
  9. Life Molecular Imaging
  10. Glaxo Wellcome R D
  11. CHDI Foundation
  12. Edmond and Lilly Safra Foundation
  13. Michael J Fox Foundation
  14. Foundation for the National Institutes of Health
  15. Canadian Institutes of Health Research
  16. Transition Therapeutics
  17. Takeda Pharmaceutical Company
  18. Servier
  19. Piramal Imaging
  20. Pfizer Inc.
  21. Novartis Pharmaceuticals Corporation
  22. Neurotrack Technologies
  23. NeuroRx Research
  24. Meso Scale Diagnostics, LLC.
  25. Lumosity
  26. Lundbeck
  27. Merck Co., Inc.
  28. Johnson & Johnson Pharmaceutical Research & Development LLC.
  29. Janssen Alzheimer Immunotherapy Research & Development, LLC.
  30. IXICO Ltd.
  31. GE Healthcare
  32. Fujarebio US
  33. Genentech, Inc.
  34. F. Hoffmann-La Roche Ltd.
  35. EuroImmun
  36. Eli Lilly and Company
  37. Elan Pharmaceuticals, Inc.
  38. Eisai, Inc.
  39. Cogstate
  40. CereSpir, Inc.
  41. Bristol-Myers Squibb Compan
  42. Biogen
  43. BioClinica, Inc.
  44. Araclon Biotech
  45. Alzheimer's Drug Discovery Foundation
  46. Alzheimer's Association
  47. AbbVie
  48. National Institute of Biomedical Imaging and Bioengineering
  49. National Institute on Aging
  50. Department of Defense [W81XWH-12-2-0012]
  51. National Institutes of Health [U01 AG024904]

向作者/读者索取更多资源

Alzheimer's disease (AD) is a devastating and progressive neurodegenerative disease for which there is no cure. Mild cognitive impairment (MCI) is considered a prodromal stage of the disease. Molecular imaging with positron emission tomography (PET) allows for the in vivo visualisation and tracking of pathophysiological changes in AD and MCI. PET is a very promising methodology for differential diagnosis and novel targets of PET imaging might also serve as biomarkers for disease-modifying therapeutic interventions. This review provides an overview of the current status and applications of in vivo molecular imaging of AD pathology, specifically amyloid, tau, and microglial activation. PET imaging studies were included and evaluated as potential biomarkers and for monitoring disease progression. Although the majority of radiotracers showed the ability to discriminate AD and MCI patients from healthy controls, they had various limitations that prevent the recommendation of a single technique or tracer as an optimal biomarker. Newer research examining amyloid, tau, and microglial PET imaging in combination suggest an alternative approach in studying the disease process.

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