| Literature DB >> 20541611 |
Markus Donix1, Alison C Burggren, Nanthia A Suthana, Prabha Siddarth, Arne D Ekstrom, Allison K Krupa, Michael Jones, Anup Rao, Laurel Martin-Harris, Linda M Ercoli, Karen J Miller, Gary W Small, Susan Y Bookheimer.
Abstract
People with the apolipoprotein-Eepsilon4 (APOE-4) genetic risk for Alzheimer's disease show morphologic differences in medial temporal lobe regions when compared to non-carriers of the allele. Using a high-resolution MRI and cortical unfolding approach, our aim was to determine the rate of cortical thinning among medial temporal lobe subregions over the course of 2 years. We hypothesized that APOE-4 genetic risk would contribute to longitudinal cortical thickness change in the subiculum and entorhinal cortex, regions preferentially susceptible to Alzheimer's disease related pathology. Thirty-two cognitively intact subjects, mean age 61 years, 16 APOE-4 carriers, 16 non-carriers, underwent baseline and follow-up MRI scans. Over this relatively brief interval, we found significantly greater cortical thinning in the subiculum and entorhinal cortex of APOE-4 carriers when compared to non-carriers of the allele. Average cortical thinning across all medial temporal lobe subregions combined was also significantly greater for APOE-4 carriers. This finding is consistent with the hypothesis that carrying the APOE-4 allele renders subjects at a higher risk for developing Alzheimer's disease. Copyright 2010 Elsevier Inc. All rights reserved.Entities:
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Year: 2010 PMID: 20541611 PMCID: PMC3118546 DOI: 10.1016/j.neuroimage.2010.06.009
Source DB: PubMed Journal: Neuroimage ISSN: 1053-8119 Impact factor: 6.556