Amyloid PET imaging in patients with mild cognitive impairment: a 2-year follow-up study

J Koivunen1, N Scheinin, J R Virta

  • 1Turku PET Centre, University of Turku, Turku, Finland.

Neurology
|February 18, 2011
PubMed
Abstract

Insights

Patients with mild cognitive impairment (MCI) converting to Alzheimer's disease (AD) show increased amyloid deposition. Brain atrophy progresses in both converters and non-converters, but amyloid changes modestly during MCI progression.

Area of Science:

  • Neuroimaging
  • Neurology
  • Alzheimer's Disease Research

Background:

  • Mild cognitive impairment (MCI) increases the risk of progression to Alzheimer's disease (AD).
  • Amyloid-beta plaque accumulation, a hallmark of AD, can be visualized using PET imaging with tracers like Carbon-11 Pittsburgh compound B ([(11)C] PiB).

Purpose of the Study:

  • To assess changes in beta-amyloid deposition in individuals with MCI over a two-year period.
  • To investigate the relationship between amyloid burden, brain atrophy, and conversion to AD.

Main Methods:

  • [(11)C] PiB PET scans, MRI, and neuropsychological tests were administered at baseline and follow-up in MCI patients.
  • Control groups were included for comparison at baseline.
  • Analysis focused on [(11)C] PiB retention and hippocampal volume changes.

Main Results:

  • MCI patients who converted to AD exhibited higher baseline [(11)C] PiB retention in several brain regions compared to non-converters.
  • While converters showed no significant change in [(11)C] PiB uptake, non-converters demonstrated an increase in specific cortical and subcortical areas.
  • Hippocampal atrophy was greater at baseline in converters and increased significantly in both groups over time.

Conclusions:

  • Amyloid deposition and hippocampal atrophy appear to follow distinct trajectories during MCI evolution towards AD.
  • Modest changes in [(11)C] PiB retention accompany significant hippocampal atrophy preceding or during conversion to AD.
  • Further longitudinal studies are necessary to determine if non-converters eventually convert, indicating potential preclinical amyloid changes.