4.6 Article

Different FDG-PET metabolic patterns at single-subject level in the behavioral variant of fronto-temporal dementia

Journal

CORTEX
Volume 83, Issue -, Pages 101-112

Publisher

ELSEVIER MASSON, CORPORATION OFFICE
DOI: 10.1016/j.cortex.2016.07.008

Keywords

Behavioral variant of fronto-temporal dementia; FDG positron emission tomography; Frontal variant of fronto-temporal dementia; Temporal variant of fronto-temporal dementia

Funding

  1. Fondazione Eli-Lilly (Eli-Lilly grant Imaging of neuroinflammation and neurodegeneration in prodromal and presymptomatic Alzheimer's disease phases)
  2. MIUR grant I meccanismi neurocognitivi alla base delle interazioni sociali [PRIN2010XPMFW4_008]
  3. Universita degli Studi di Milano-Bicocca grant Dottorato ad Alta Formazione in Psicologia Sperimentale, Linguistica e Neuroscienze Cognitive
  4. EU FP7 INMIND Project [278850, FP7-HEALTH-201]

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Background: The diagnosis of probable behavioral variant of fronto-temporal dementia (bvFTD) according to current criteria requires the imaging evidence of frontal and/or anterior temporal atrophy or hypoperfusion/hypometabolism. Different variants of this pattern of brain involvement may, however, be found in individual cases, supporting the presence of heterogeneous phenotypes. Objective: We examined in a case-by-case approach the FDG-PET metabolic patterns of patients fulfilling clinical criteria for probable bvFTD, assessing the presence and frequency of specific FDG-PET features. Materials and methods: Fifty two FDG-PET scans of probable bvFTD patients were retrospectively analyzed together with clinical and neuropsychological data. Neuroimaging experts rated the FDG-PET hypometabolism maps obtained at the single-subject level with optimized voxel-based Statistical Parametric Mapping (SPM). The functional metabolic heterogeneity was further tested by hierarchical cluster analysis and principal component analysis (PCA). Results: Both the SPM maps and cluster analysis identified two major variants of cerebral hypometabolism, namely the frontal and the temporo-limbic, which were correlated with different cognitive profiles. Executive and language deficits were the cognitive hallmark in the frontal subgroup, while poor encoding and recall on long-term memory tasks was typical of the temporo-limbic subgroup. Discussion: SPM single-subject analysis indicates distinct patterns of brain dysfunction in bvFTD, coupled with specific clinical features, suggesting different profiles of neurode-generative vulnerability. These findings have important implications for the early diagnosis of bvFTD and for the application of the recent international consensus criteria. (C) 2016 Elsevier Ltd. All rights reserved.

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