4.7 Article

Association of brain amyloid-β with cerebral perfusion and structure in Alzheimer's disease and mild cognitive impairment

Journal

BRAIN
Volume 137, Issue -, Pages 1550-1561

Publisher

OXFORD UNIV PRESS
DOI: 10.1093/brain/awu043

Keywords

Alzheimer's disease; beta-amyloid; PET imaging; perfusion imaging; magnetic resonance imaging

Funding

  1. Alzheimer's Disease Neuroimaging Initiative (National Institutes of Health) [U01 AG024904]
  2. National Institute on Ageing
  3. National Institute of Biomedical Imaging and Bioengineering
  4. Canadian Institutes of Health Research
  5. NIH [P30 AG010129, K01 AG030514]
  6. Swedish Research Council
  7. Goteborgs Lakaresallskap
  8. Svenska Lakaresallskapet
  9. Sahlgrenska Universitetssjukhuset
  10. Carl-Bertil Laurells fond
  11. Klinisk Biokemi i Norden

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Patients with Alzheimer's disease have reduced cerebral blood flow measured by arterial spin labelling magnetic resonance imaging, but it is unclear how this is related to amyloid-beta pathology. Using 182 subjects from the Alzheimer's Disease Neuroimaging Initiative we tested associations of amyloid-beta with regional cerebral blood flow in healthy controls (n = 51), early (n = 66) and late (n = 41) mild cognitive impairment, and Alzheimer's disease with dementia (n = 24). Based on the theory that Alzheimer's disease starts with amyloid-beta accumulation and progresses with symptoms and secondary pathologies in different trajectories, we tested if cerebral blood flow differed between amyloid-beta-negative controls and -positive subjects in different diagnostic groups, and if amyloid-beta had different associations with cerebral blood flow and grey matter volume. Global amyloid-beta load was measured by florbetapir positron emission tomography, and regional blood flow and volume were measured in eight a priori defined regions of interest. Cerebral blood flow was reduced in patients with dementia in most brain regions. Higher amyloid-beta load was related to lower cerebral blood flow in several regions, independent of diagnostic group. When comparing amyloid-beta-positive subjects with -negative controls, we found reductions of cerebral blood flow in several diagnostic groups, including in precuneus, entorhinal cortex and hippocampus (dementia), inferior parietal cortex (late mild cognitive impairment and dementia), and inferior temporal cortex (early and late mild cognitive impairment and dementia). The associations of amyloid-beta with cerebral blood flow and volume differed across the disease spectrum, with high amyloid-beta being associated with greater cerebral blood flow reduction in controls and greater volume reduction in late mild cognitive impairment and dementia. In addition to disease stage, amyloid-beta pathology affects cerebral blood flow across the span from controls to dementia patients. Amyloid-beta pathology has different associations with cerebral blood flow and volume, and may cause more loss of blood flow in early stages, whereas volume loss dominates in late disease stages.

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