Alzheimer’s & Dementia: Diagnosis, Assessment & Disease Monitoring (Jan 2020)

Topographical distribution of Aβ predicts progression to dementia in Aβ positive mild cognitive impairment

  • Tharick A. Pascoal,
  • Joseph Therriault,
  • Sulantha Mathotaarachchi,
  • Min Su Kang,
  • Monica Shin,
  • Andrea L. Benedet,
  • Mira Chamoun,
  • Cecile Tissot,
  • Firoza Lussier,
  • Sara Mohaddes,
  • Jean‐Paul Soucy,
  • Gassan Massarweh,
  • Serge Gauthier,
  • Pedro Rosa‐Neto,
  • for the Alzheimer's Disease Neuroimaging Initiative

DOI
https://doi.org/10.1002/dad2.12037
Journal volume & issue
Vol. 12, no. 1
pp. n/a – n/a

Abstract

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Abstract Introduction Abnormal brain amyloid beta (Aβ) is typically assessed in vivo using global concentrations from cerebrospinal fluid and positron emission tomography (PET). However, it is unknown whether the assessment of the topographical distribution of Aβ pathology can provide additional information to identify, among global Aβ positive individuals, those destined for dementia. Methods We studied 260 amnestic mild cognitive impairment (MCI) subjects who were Aβ‐PET positive with [18F]florbetapir. Using [18F]florbetapir, we assessed the percentage of voxels sowing Aβ abnormality as well as the standardized uptake value ratio (SUVR) values across brain regions. Regressions tested the predictive effect of Aβ on progression to dementia over 2 years. Results Neither global nor regional [18F]florbetapir SUVR concentrations predicted progression to dementia. In contrast, the spatial extent of Aβ pathology in regions comprising the default mode network was highly associated with the development of dementia over 2 years. Discussion These results highlight that the regional distribution of Aβ abnormality may provide important complementary information at an individual level regarding the likelihood of Aβ positive MCI to progress to dementia.

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