4.7 Article

Using machine learning to quantify structuralMRIneurodegeneration patterns of Alzheimer's disease into dementia score: Independent validation on 8,834 images from ADNI, AIBL, OASIS, and MIRIAD databases

Journal

HUMAN BRAIN MAPPING
Volume 41, Issue 14, Pages 4127-4147

Publisher

WILEY
DOI: 10.1002/hbm.25115

Keywords

Alzheimer's disease; cross-database independent validation; dementia of Alzheimer's type; dementia score; disease progression; ensemble learning; longitudinal diagnostic stratification; magnetic resonance imaging; probabilistic classifier; prognosis prediction

Funding

  1. Wellcome Trust [091593/Z/10/Z]
  2. National Institute for Health Research (NIHR)
  3. EPSRC [EP/H046410/1]
  4. Medical Research Council [MR/J014257/1]
  5. UK Alzheimer's Society
  6. Foundation for the National Institutes of Health
  7. Canadian Institutes of Health Research
  8. Takeda Pharmaceutical Company
  9. Pfizer Inc.
  10. Novartis Pharmaceuticals Corporation
  11. Neurotrack Technologies
  12. Meso Scale Diagnostics, LLC
  13. Merck Co., Inc.
  14. Johnson & Johnson Pharmaceutical Research & Development LLC
  15. IXICO Ltd.
  16. GE Healthcare
  17. Fujirebio US
  18. F. HoffmannLa Roche Ltd
  19. Eli Lilly and Company
  20. Elan Pharmaceuticals, Inc.
  21. Eisai Inc.
  22. Cogstate
  23. CereSpir, Inc.
  24. Bristol-Myers Squibb Company
  25. Biogen
  26. Araclon Biotech
  27. Alzheimer's Drug Discovery Foundation
  28. Alzheimer's Association
  29. National Institute of Biomedical Imaging and Bioengineering [R01 AG055121-01A1]
  30. Department of Defense [W81XWH-12-2-0012]
  31. National Institutes of Health [U01 AG024904]
  32. Alzheimer's Disease Neuroimaging Initiative (ADNI)
  33. National Institute on Aging
  34. Pacific Alzheimer's Research Foundation
  35. Foundation Brain Canada
  36. Canadian Institutes of Health Research (CIHR)
  37. National Science Engineering Research Council (NSERC)
  38. Alzheimer Society Research Program [ASRP 19-09]
  39. GlaxoSmithKline
  40. Transition Therapeutics
  41. Servier
  42. Piramal Imaging
  43. NeuroRx Research
  44. Lundbeck
  45. Lumosity
  46. Janssen Alzheimer Immunotherapy Research & Development, LLC
  47. Genentech
  48. EuroImmun
  49. BioClinica, Inc.
  50. AbbVie
  51. Michael Smith Foundation for Health Research (MSFHR)
  52. Engineering and Physical Sciences Research Council [EP/H046410/1] Funding Source: researchfish

Ask authors/readers for more resources

Biomarkers for dementia of Alzheimer's type (DAT) are sought to facilitate accurate prediction of the disease onset, ideally predating the onset of cognitive deterioration. T1-weighted magnetic resonance imaging (MRI) is a commonly used neuroimaging modality for measuring brain structure in vivo, potentially providing information enabling the design of biomarkers for DAT. We propose a novel biomarker using structural MRI volume-based features to compute a similarity score for the individual's structural patterns relative to those observed in the DAT group. We employed ensemble-learning framework that combines structural features in most discriminative ROIs to create an aggregate measure of neurodegeneration in the brain. This classifier is trained on 423 stable normal control (NC) and 330 DAT subjects, where clinical diagnosis is likely to have the highest certainty. Independent validation on 8,834 unseen images from ADNI, AIBL, OASIS, and MIRIAD Alzheimer's disease (AD) databases showed promising potential to predict the development of DAT depending on the time-to-conversion (TTC). Classification performance on stable versus progressive mild cognitive impairment (MCI) groups achieved an AUC of 0.81 for TTC of 6 months and 0.73 for TTC of up to 7 years, achieving state-of-the-art results. The output score, indicating similarity to patterns seen in DAT, provides an intuitive measure of how closely the individual's brain features resemble the DAT group. This score can be used for assessing the presence of AD structural atrophy patterns in normal aging and MCI stages, as well as monitoring the progression of the individual's brain along with the disease course.

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