4.6 Article

Distinct Interplay Between Atrophy and Hypometabolism in Alzheimer's Versus Semantic Dementia

Journal

CEREBRAL CORTEX
Volume 29, Issue 5, Pages 1889-1899

Publisher

OXFORD UNIV PRESS INC
DOI: 10.1093/cercor/bhy069

Keywords

Alzheimer's disease; FDG-PET; multimodal neuroimaging; neurodegeneration; progressive Aphasia; semantic variant primary

Categories

Funding

  1. Ministere de la Sante [PHRCI 2008-A01150-55, PHRCN 2011 A01493-38, PHRCN 2012 12-006-0347]
  2. Agence Nationale de la Recherche (ANR) [07LVIE 006]
  3. Fondation Plan Alzheimer (Alzheimer Plan 2008-2012)
  4. Association France Alzheimer et maladies apparentees (AAP 2013)
  5. Fondation pour la Recherche Medicale (FRM)
  6. Conseil Regional de Haute Normandie
  7. Institut national de la Sante et de la recherche medicale (INSERM)

Ask authors/readers for more resources

Multimodal neuroimaging analyses offer additional information beyond that provided by each neuroimaging modality. Thus, direct comparisons and correlations between neuroimaging modalities allow revealing disease-specific topographic relationships. Here, we compared the topographic discrepancies between atrophy and hypometabolism in two neurodegenerative diseases characterized by distinct pathological processes, namely Alzheimer's disease (AD) versus semantic dementia (SD), to unravel their specific influence on local and global brain structure-function relationships. We found that intermodality topographic discrepancies clearly distinguished the two patient groups: AD showed marked discrepancies between both alterations, with greater hypometabolism than atrophy in large posterior associative neocortical regions, while SD showed more topographic consistency between atrophy and hypometabolism across brain regions. These findings likely reflect the multiple pathologies versus the relatively unitary pathological process underlying AD versus SD respectively. Our results evidence that multimodal neuroimaging-derived indexes can provide clinically relevant information to discriminate the two diseases, and potentially reveal distinct neuropathological processes.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.6
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available