4.2 Article

APOE and Spatial Navigation in Amnestic MCI: Results From a Computer-Based Test

期刊

NEUROPSYCHOLOGY
卷 28, 期 5, 页码 676-684

出版社

AMER PSYCHOLOGICAL ASSOC
DOI: 10.1037/neu0000072

关键词

mild cognitive impairment; apolipoprotein E; hippocampus; Hidden Goal Task; neuropsychology

资金

  1. Grant Agency of the Czech Republic [309/09/1053, 309/09/0286]
  2. Grant Agency of Charles University in Prague [624012, 546113]
  3. Internal Grant Agency of the Ministry of Health of the Czech Republic [NT11225-4]
  4. European Regional Development Fund-Project FNUSA-ICRC [CZ.1.05/1.1.00/02.0123]
  5. European Social Fund
  6. State Budget of the Czech Republic
  7. European Social Fund within the project Young Talent Incubator II [CZ.1.07/2.3.00/20.0117]
  8. Ministry of Health, Czech Republic-conceptual development of research organization, University Hospital Motol, Prague, Czech Republic [00064203]
  9. CTSA from the National Center for Advancing Translational Sciences (NCATS), a component of the National Institutes of Health (NIH) [UL1 TR000135]
  10. [2/2012 (699002)]
  11. [AV0Z50110509]
  12. [RVO:67985823]

向作者/读者索取更多资源

Objective: We investigated the association between APOE epsilon 4 status and spatial navigation in patients with amnestic mild cognitive impairment (aMCI) and assessed the role of hippocampal volume in this association. Method: Participants were 74 patients with clinically confirmed aMCI (33 APOE epsilon 4 noncarriers, 26 heterozygous, and 15 homozygous epsilon 4 carriers). Body-centered (egocentric) and world-centered (allocentric) spatial navigation in a computerized human analogue of the Morris Water Maze was assessed. Brain MRI with subsequent automated hippocampal volumetry was included. Results: Groups were similar in neuropsychological profile. Controlling for age, sex, education, and free memory recall, the APOE epsilon 4 carriers performed more poorly on all spatial navigation subtasks (ps < .05). APOE epsilon 4 homozygotes performed worse than heterozygotes (p = .021). Right hippocampal volume accounted for the differences in allocentric and delayed subtasks (ps > .05), but not in the egocentric subtask (p < .001). Conclusions: Using an easy-to-use, computer-based tool to assess spatial navigation, we found spatial navigation deficits to worsen in a dose-dependent manner as a function of APOE epsilon 4 status. This was at least partially due to differences in right hippocampal volume.

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