Cerebral atrophy in mild cognitive impairment and Alzheimer disease: rates and acceleration

Kelvin K Leung1, Jonathan W Bartlett, Josephine Barnes

  • 1Dementia Research Centre, UCL Institute of Neurology, Queen Square, London, UK.

Neurology
|January 11, 2013
PubMed
Abstract

Insights

Brain atrophy accelerates in mild cognitive impairment (MCI) and Alzheimer disease (AD) patients, particularly in the hippocampus and ventricles. This acceleration suggests a prolonged transition to advanced Alzheimer disease pathology.

Area of Science:

  • Neuroscience
  • Medical Imaging
  • Gerontology

Background:

  • Alzheimer disease (AD) is characterized by progressive neurodegeneration.
  • Mild cognitive impairment (MCI) represents an intermediate stage between normal aging and AD.
  • Quantifying atrophy rates and their acceleration is crucial for understanding disease progression.

Purpose of the Study:

  • To quantify regional and global cerebral atrophy rates.
  • To assess atrophy acceleration in healthy controls, MCI, and mild AD.
  • To identify patterns of neurodegeneration over time.

Main Methods:

  • Utilized MRI scans from the Alzheimer's Disease Neuroimaging Initiative (ADNI) database.
  • Analyzed scans at 0, 6, 12, 18, 24, and 36 months.
  • Calculated volume changes (whole brain, hippocampus, ventricles) using boundary shift integral.

Main Results:

  • No acceleration in whole-brain atrophy rates observed in any group.
  • Significant acceleration in hippocampal atrophy rates in MCI subjects (0.22%/year²).
  • Accelerated ventricular enlargement in MCI (0.27 mL/year²) and AD (0.88 mL/year²) subjects.

Conclusions:

  • Observed acceleration rates suggest a lengthy transition period to AD-related pathology.
  • Hippocampal atrophy acceleration in MCI is linked to progression to clinical AD.
  • Ventricular enlargement acceleration is evident in both MCI and AD stages.

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