4.7 Article

Hippocampal Atrophy Patterns in Mild Cognitive Impairment and Alzheimer's Disease

Journal

HUMAN BRAIN MAPPING
Volume 31, Issue 9, Pages 1339-1347

Publisher

WILEY
DOI: 10.1002/hbm.20934

Keywords

hippocampal subfields; Alzheimer's disease; manual parcellation; MRI

Funding

  1. National Institutes of Health [RO1 AG010897, P01 AG12435]

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Background: Histopathological studies and animal models suggest that hippocampal subfields may be differently affected by aging, Alzheimer's disease (AD), and other diseases High-resolution images at 4 Tesla depict details of the internal structure of the hippocampus allowing for in vivo volummetry of different subfields The aims of this study were as follows (1) to determine patterns of volume loss in hippocampal subfields in normal aging, AD, and amnestic mild cognitive impairment (MCI). (2) To determine if measurements of hippocampal subfields provide advantages over total hippocampal volume for differentiation between groups Methods. Ninety-one subjects (53 controls (mean age: 69 3 +/- 73), 20 MCI (mean age: 73.6 +/- 7 1), and 18 AD (mean age: 69 1 +/- 9.5) were studied with a high-resolution T2 weighted imaging sequence aimed at the hippocampus Entorhinal cortex (ERC), subiculum, CA1, CA1-CA2 transition zone (CA1-2), CA3 & dentate gyrus (CA3&DG) were manually marked in the anterior third of the hippocampal body. Hippocampal volume was obtained from the Freesurfer and manually edited Results Compared to controls, AD had smaller volumes of ERC, subiculum, CA1, CA1-2, and total hippocampal volumes. MCI had smaller CA1-2 volumes Discriminant analysis and power analysis showed that CA1-2 was superior to total hippocampal volume for distinction between controls and MCI Conclusion. The patterns of subfield atrophy in AD and MCI were consistent with patterns of neuronal cell loss/reduced synaptic density described by histopathology. These preliminary findings suggest that hippocampal subfield volumetry might be a better measure for diagnosis of early AD and for detection of other disease effects than measurement of total hippocampus Hum Brain Mapp 31 1339-1347, 2010 (C) 2010 Wiley-Liss. Inc.

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