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Staging Alzheimer's disease progression with multimodality neuroimaging
Authors:Ewers Michael  Frisoni Giovanni B  Teipel Stefan J  Grinberg Lea T  Amaro Edson  Heinsen Helmut  Thompson Paul M  Hampel Harald
Affiliation:Department of Radiology, University of California at San Francisco, San Francisco, USA. michael.ewers@ucsf.edu
Abstract:Rapid developments in medical neuroimaging have made it possible to reconstruct the trajectory of Alzheimer's disease (AD) as it spreads through the living brain. The current review focuses on the progressive signature of brain changes throughout the different stages of AD. We integrate recent findings on changes in cortical gray matter volume, white matter fiber tracts, neuropathological alterations, and brain metabolism assessed with molecular positron emission tomography (PET). Neurofibrillary tangles accumulate first in transentorhinal and cholinergic brain areas, and 4-D maps of cortical volume changes show early progressive temporo-parietal cortical thinning. Findings from diffusion tensor imaging (DTI) for assessment fiber tract integrity show cortical disconnection in corresponding brain networks. Importantly, the developmental trajectory of brain changes is not uniform and may be modulated by several factors such as onset of disease mechanisms, risk-associated and protective genes, converging comorbidity, and individual brain reserve. There is a general agreement between in vivo brain maps of cortical atrophy and amyloid pathology assessed through PET, reminiscent of post mortem histopathology studies that paved the way in the staging of AD. The association between in vivo and post mortem findings will clarify the temporal dynamics of pathophysiological alterations in the development of preclinical AD. This will be important in designing effective treatments that target specific underlying disease AD mechanisms.
Keywords:Aβ, amyloid-beta   AD, Alzheimer's disease   ADNI, Alzheimer's Disease Neuroimaging Initiative   ApoE4, apolipoprotein ?4   BDNF, brain derived neurotrophic factor   CSF, cerebrospinal fluid   DTI, diffusion tensor imaging   FA, fractional anisotropy   FDG-PET, fluoro-deoxyglucose positron emission tomography   MCI, mild cognitive impairment   MRI, magnetic resonance imaging   MTR, magnetic transfer ratio   NbM, basal nucleus of Meynert   [11C]PIB, Pittsburgh Compound B
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