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Published on: June 26, 2013
Mapping brain morphological and functional conversion patterns in amnestic MCI: a voxel-based MRI and FDG-PET study
Silvia Morbelli1, Arnoldo Piccardo, Giampiero Villavecchia
1Nuclear Medicine Unit, Department of Internal Medicine, University of Genoa, Viale Benedetto XV, 6, 16132 Genoa, Italy. silviadaniela.morbelli@hsanmartino.it
European Journal of Nuclear Medicine and Molecular Imaging
|August 8, 2009
Summary
Early Alzheimer disease (AD) detection in amnestic mild cognitive impairment (aMCI) shows distinct brain changes. Posterior cingulate-precuneus hypometabolism signals memory issues, while left temporal cortex changes predict conversion to AD.
Area of Science:
- Neuroimaging
- Neurology
- Alzheimer's Disease Research
Background:
- Amnestic mild cognitive impairment (aMCI) is a prodromal stage for Alzheimer disease (AD).
- Understanding the transition from aMCI to AD requires identifying early neurobiological markers.
Purpose of the Study:
- To investigate the morphological and functional brain changes associated with memory impairment in aMCI.
- To identify substrates predicting conversion from aMCI to Alzheimer disease.
Main Methods:
- Utilized brain MRI and FDG-PET in 20 aMCI patients and 12 controls.
- Tracked conversion to AD over a 2-year follow-up period.
- Compared grey matter density and glucose metabolism between converters, non-converters, and controls using SPM2.
Main Results:
- Converters showed reduced grey matter in the parahippocampal gyrus and thalami compared to controls.
- Hypometabolism was observed in the precuneus and posterior cingulate gyrus in both converters and non-converters versus controls.
- Converters exhibited greater hypometabolism in the left temporal cortex compared to non-converters.
Conclusions:
- Discrepancies between atrophy and hypometabolism, characteristic of AD, are evident at the aMCI stage.
- Posterior cingulate-precuneus hypometabolism may indicate early memory deficits.
- Left temporal cortex hypometabolism appears to be a marker for progression to Alzheimer disease.
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