Basal Forebrain and Hippocampus as Predictors of Conversion to Alzheimer's Disease in Patients with Mild Cognitive Impairment - A Multicenter DTI and Volumetry Study

J Alzheimers Dis. 2015;48(1):197-204. doi: 10.3233/JAD-150063.

Abstract

Background: Hippocampal grey matter (GM) atrophy predicts conversion from mild cognitive impairment (MCI) to Alzheimer's disease (AD). Pilot data suggests that mean diffusivity (MD) in the hippocampus, as measured with diffusion tensor imaging (DTI), may be a more accurate predictor of conversion than hippocampus volume. In addition, previous studies suggest that volume of the cholinergic basal forebrain may reach a diagnostic accuracy superior to hippocampal volume in MCI.

Objective: The present study investigated whether increased MD and decreased volume of the hippocampus, the basal forebrain and other AD-typical regions predicted time to conversion from MCI to AD dementia.

Methods: 79 MCI patients with DTI and T1-weighted magnetic resonance imaging (MRI) were retrospectively included from the European DTI Study in Dementia (EDSD) dataset. Of these participants, 35 converted to AD dementia after 6-46 months (mean: 21 months). We used Cox regression to estimate the relative conversion risk predicted by MD values and GM volumes, controlling for age, gender, education and center.

Results: Decreased GM volume in all investigated regions predicted an increased risk for conversion. Additionally, increased MD in the right basal forebrain predicted increased conversion risk. Reduced volume of the right hippocampus was the only significant predictor in a stepwise model combining all predictor variables.

Conclusion: Volume reduction of the hippocampus, the basal forebrain and other AD-related regions was predictive of increased risk for conversion from MCI to AD. In this study, volume was superior to MD in predicting conversion.

Keywords: Alzheimer’s disease; Diffusion tensor imaging; Mild Cognitive Impairment; atrophy; basal forebrain; cholinergic; early diagnosis; magnetic resonance imaging.

Publication types

  • Multicenter Study

MeSH terms

  • Aged
  • Aged, 80 and over
  • Alzheimer Disease / complications
  • Alzheimer Disease / diagnosis*
  • Atrophy
  • Basal Forebrain / pathology*
  • Cognitive Dysfunction / complications
  • Cognitive Dysfunction / pathology*
  • Diffusion Tensor Imaging*
  • Disease Progression
  • Europe
  • Female
  • Hippocampus / pathology*
  • Humans
  • International Cooperation
  • Magnetic Resonance Imaging
  • Male
  • Mental Status Schedule
  • Neuropsychological Tests
  • Predictive Value of Tests
  • Statistics, Nonparametric