| Literature DB >> 27981671 |
Alexandre Bejanin1,2,3,4, Béatrice Desgranges1,2,3,4, Renaud La Joie1,2,3,4, Brigitte Landeau1,2,3,4, Audrey Perrotin1,2,3,4, Florence Mézenge1,2,3,4, Serge Belliard1,2,3,5, Vincent de La Sayette1,2,3,4,6, Francis Eustache1,2,3,4, Gaël Chételat1,2,3,4.
Abstract
This study aims at further understanding the distinct vulnerability of brain networks in Alzheimer's disease (AD) versus semantic dementia (SD) investigating the white matter injury associated with medial temporal lobe (MTL) atrophy in both conditions. Twenty-six AD patients, twenty-one SD patients, and thirty-nine controls underwent a high-resolution T1-MRI scan allowing to obtain maps of grey matter volume and white matter density. A statistical conjunction approach was used to identify MTL regions showing grey matter atrophy in both patient groups. The relationship between this common grey matter atrophy and white matter density maps was then assessed within each patient group. Patterns of grey matter atrophy were distinct in AD and SD but included a common region in the MTL, encompassing the hippocampus and amygdala. This common atrophy was associated with alterations in different white matter areas in AD versus SD, mainly including the cingulum and corpus callosum in AD, while restricted to the temporal lobe - essentially the uncinate and inferior longitudinal fasciculi - in SD. Complementary analyses revealed that these relationships remained significant when controlling for global atrophy or disease severity. Overall, this study provides the first evidence that atrophy of the same MTL region is related to damage in distinct white matter fibers in AD and SD. These different patterns emphasize the vulnerability of distinct brain networks related to the MTL in these two disorders, which might underlie the discrepancy in their symptoms. These results further suggest differences between AD and SD in the neuropathological processes occurring in the MTL. Hum Brain Mapp 38:1791-1800, 2017.Entities:
Keywords: Alzheimer's disease; hippocampus; medial temporal lobe; primary progressive aphasia; semantic dementia; white matter
Mesh:
Year: 2016 PMID: 27981671 PMCID: PMC6866822 DOI: 10.1002/hbm.23482
Source DB: PubMed Journal: Hum Brain Mapp ISSN: 1065-9471 Impact factor: 5.038