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Abstract Details

Characterization of language features of subtypes of primary progressive aphasia based on clustering analysis of brain metabolism
Aging, Dementia, and Behavioral Neurology
P3 - Poster Session 3 (5:30 PM-6:30 PM)
9-002

Our aim was to study the language and cognitive features associated to a new proposal of classification of primary progressive aphasia (PPA).

Primary progressive aphasia (PPA) is a clinical syndrome of neurodegenerative origin. Currently, three main variants (non-fluent, semantic, and logopenic) are recognized with the last consensus criteria published in 2011. This classification has improved the clinical-pathological correlation. However, there is some controversy about the existence of some additional subtypes.

68 patients with PPA in mild or early stages of the disease and 20 healthy controls were assessed with a comprehensive language and cognitive protocol. They were also evaluated with 18F-FDG-PET. Patients were classified according to FDG-PET regional metabolism using a previously developed and validated lgorithm based on a hierarchical agglomerative cluster analysis with Ward’s linkage method. Five variants were found, which mainly resulted from splitting both non-fluent and logopenic variants into two subtypes. 

Non-fluent type 1 showed a greater impairment in repetition of sentences and reading of irregular words in comparison to non-fluent type 2. Conversely, this group showed a higher degree of apraxia of speech. Non-fluent type 1 differed from both logopenic subtypes only in buccofacial apraxia, which was more impaired in non-fluent type 1. Logopenic variant type 1 showed a greater degree of impairment in action naming in comparison to logopenic type 2. Each subtype of PPA was associated to specific brain regions in voxel-based brain mapping analysis. 

Our study supports the existence of five variants of PPA. These variants show some differences in language and FDG-PET imaging characteristics. Future studies should determine if this classification could improve the clinical-pathological correlation. 

Authors/Disclosures
Jordi A. Matias-Guiu
PRESENTER
No disclosure on file
No disclosure on file
No disclosure on file
Vanesa Pytel No disclosure on file
No disclosure on file
No disclosure on file
Jorge Matias Guiu Guia, MD (Hospital Clinico San Carlos) No disclosure on file