4.7 Article

An MRI measure of degenerative and cerebrovascular pathology in Alzheimer disease

期刊

NEUROLOGY
卷 91, 期 15, 页码 E1402-E1412

出版社

LIPPINCOTT WILLIAMS & WILKINS
DOI: 10.1212/WNL.0000000000006310

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资金

  1. NIH [P01AG007232, R01AG037212, RF1AG054023, R01AG034189, R56AG034189]
  2. National Center for Advancing Translational Sciences, NIH [UL1TR001873]
  3. Alzheimer's Disease Neuroimaging Initiative (ADNI) (NIH) [U01 AG024904]
  4. DOD ADNI (Department of Defense) [W81XWH-12-2-0012]
  5. National Institute on Aging
  6. National Institute of Biomedical Imaging and Bioengineering
  7. Alzheimer's Association
  8. Alzheimer's Drug Discovery Foundation
  9. Araclon Biotech
  10. Biogen
  11. Bristol-Myers Squibb Company
  12. CereSpir, Inc.
  13. Cogstate
  14. Elan Pharmaceuticals, Inc.
  15. Eli Lilly and Company
  16. EuroImmun
  17. Fujirebio
  18. Johnson & Johnson Pharmaceutical Research & Development LLC.
  19. Merck Co., Inc.
  20. Meso Scale Diagnostics
  21. NeuroRx Research
  22. Novartis Pharmaceuticals Corporation
  23. Pfizer Inc.
  24. Piramal Imaging
  25. Takeda Pharmaceutical Company
  26. Canadian Institutes of Health Research
  27. Northern California Institute for Research and Education
  28. AbbVie
  29. BioClinica, Inc.
  30. Eisai Inc.
  31. F. Hoffmann-La Roche Ltd.
  32. Genentech, Inc.
  33. GE Healthcare
  34. IXICO Ltd.
  35. Janssen Alzheimer Immunotherapy Research & Development, LLC.
  36. Lumosity
  37. Lundbeck
  38. Meso Scale Diagnostics, LLC.
  39. Neurotrack Technologies
  40. Piramal Imaging
  41. Servier
  42. Transition Therapeutics

向作者/读者索取更多资源

Objective To develop, replicate, and validate an MRI-based quantitative measure of both cerebrovascular and neurodegeneration in Alzheimer disease (AD) for clinical and potentially research purposes. Methods We used data from a cross-sectional and longitudinal community-based study of Medicare-eligible residents in northern Manhattan followed every 18-24 months (n = 1,175, mean age 78 years). White matter hyperintensities, infarcts, hippocampal volumes, and cortical thicknesses were quantified from MRI and combined to generate an MRI measure associated with episodic memory. The combined MRI measure was replicated and validated using autopsy data, clinical diagnoses, and CSF biomarkers and amyloid PET from the Alzheimer's Disease Neuroimaging Initiative. Results The quantitative MRI measure was developed in a group of community participants (n = 690) and replicated in a similar second group (n = 485). Compared with healthy controls, the quantitative MRI measure was lower in patients with mild cognitive impairment and lower still in those with clinically diagnosed AD. The quantitative MRI measure correlated with neurofibrillary tangles, neuronal loss, atrophy, and infarcts at postmortem in an autopsy subset and was also associated with PET amyloid imaging and CSF levels of total tau, phosphorylated tau, and beta-amyloid 42. The MRI measure predicted conversion to MCI and clinical AD among healthy controls. Conclusion We developed, replicated, and validated an MRI measure of cerebrovascular and neurodegenerative pathologies that are associated with clinical and neuropathologic diagnosis of AD and related to established biomarkers.

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