Discrimination of normal aging, MCI and AD with multimodal imaging measures on the medial temporal lobe

Psychiatry Res. 2010 Sep 30;183(3):237-43. doi: 10.1016/j.pscychresns.2010.03.006. Epub 2010 Aug 11.

Abstract

This study aimed to compare the discrimination accuracy of hippocampal volume (HC-Vol), parahippocampal cingulum fractional anisotropy (PHC-FA), hippocampal glucose metabolism (HC-Glu), and any combination of the three measurements among normal control (NC), mild cognitive impairment (MCI), and Alzheimer's disease (AD). Three-dimensional MRI, diffusion tensor imaging, and FDG-PET were applied to age- and gender-matched 17 NC, 17 MCI, and 17 mild AD patients. Subjects also underwent a neuropsychological test battery including three verbal episodic memory tests. Logistic regression analyses were systematically conducted to select the best model for between-group discrimination. PHC-FA plus HC-Vol model, HC-Glu only model, and the model combining all three modalities were finally chosen for NC vs. MCI (discrimination accuracy: 79.4%), MCI vs. AD (73.5%), and NC vs. AD discrimination (94.1%), respectively. All the three imaging measures also showed significant correlation with all three episodic memory tests. These findings support that each imaging measure, respectively, and their combination have a stage-specific potential as a useful neuroimaging marker for detection and progression monitoring of early stage of AD.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aged
  • Aging / pathology*
  • Alzheimer Disease / diagnostic imaging
  • Alzheimer Disease / pathology*
  • Analysis of Variance
  • Brain Mapping
  • Cognition Disorders / diagnostic imaging
  • Cognition Disorders / pathology*
  • Female
  • Hippocampus / pathology
  • Humans
  • Imaging, Three-Dimensional / methods
  • Logistic Models
  • Magnetic Resonance Imaging / methods
  • Male
  • Memory / physiology
  • Middle Aged
  • Neuropsychological Tests
  • Positron-Emission Tomography / methods
  • Temporal Lobe / diagnostic imaging
  • Temporal Lobe / pathology*