Amyloid beta (Aβ or Abeta) is a peptide of 36–43 amino acids that is processed from the Amyloid precursor protein. While best known as a component of amyloid plaques in association with Alzheimer's disease, evidence has been found that Aβ is a highly multifunctional peptide with significant non-pathological activity.[1] Aβ is the main component of deposits found in the brains of patients with Alzheimer's disease
Beta Amyloid~Classification of Amyloid-Positivity in Controls: Comparison of Visual Read and Quantitative Approaches.
An important research application of amyloid imaging with positron emission tomography (PET) is detection of the earliest evidence of fibrillar amyloid-beta (Aβ) deposition. Use of amyloid
PET for this purpose, requires a reproducible method for defining a
cutoff that separates individuals with no significant Aβ deposition from
those in which Aβ deposition has begun. We previously reported the
iterative outlier approach (IO) for the analysis of Pittsburgh
Compound-B (PiB) PET data. Developments in amyloid
imaging since the initial report of IO have led us to re-examine the
generalizability of this method. IO was developed using full-dynamic
atrophy-corrected PiB PET data obtained from a group of control subjects
with a fairly distinct separation between PiB-positive [PiB(+)] and
PiB-negative [PiB(-)] subjects. METHODS: We tested the performance of IO
using late-summed tissue ratio data with atrophy correction or with an
automated template method without atrophy correction and tested the
robustness of the method when applied to a cohort of older subjects in
which separation between PiB(+) and PiB(-) subjects was not so distinct.
RESULTS: The IO method did not perform consistently across analyses and
performed particularly poorly when separation was less clear. We found
that a sparse k-means (SKM) cluster analysis approach performed
significantly better; performing more consistently across methods and
subject cohorts. We also compared SKM to a consensus visual read
approach and found very good correspondence. Conclusion The visual read
and SKM methods, applied together, may optimize the identification of
early Aβ deposition. These methods have the potential to provide a
standard approach to the detection of PiB-positivity that is
generalizable across centers.
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