Longitudinal naming and repetition relates to AD pathology and burden in autopsy-confirmed primary progressive aphasia

Alzheimers Dement (N Y). 2021 Aug 2;7(1):e12188. doi: 10.1002/trc2.12188. eCollection 2021.

Abstract

Introduction: In primary progressive aphasia (PPA) patients with autopsy-confirmed Alzheimer's disease (AD) or frontotemporal lobar degeneration (FLTD), we tested how the core clinical features of logopenic PPA-naming and repetition-change over time and relate to pathologic burden.

Methods: In PPA with AD (n = 13) or FTLD (n = 16) pathology, Boston Naming Test and Forward Digit Span measured longitudinal naming and repetition; as reference, Mini-Mental State Examination (MMSE) measured global cognition. Pathologic burden in left peri-Sylvian regions was related to longitudinal cognitive decline.

Results: PPA with AD showed greater decline in naming (P = 0.021) and repetition (P = 0.020), compared to FTLD; there was no difference in MMSE decline (P = 0.99). Across all PPA, declining naming (P = 0.0084) and repetition (P = 0.011) were associated with angular, superior-middle temporal (naming P = 0.014; repetition P = 0.011) and middle frontal (naming P = 0.041; repetition P = 0.030) pathologic burden.

Discussion: Unique longitudinal profiles of naming and repetition performance in PPA with AD are related to left peri-Sylvian pathology.

Keywords: Alzheimer's disease; frontotemporal lobar degeneration; primary progressive aphasia.