Hemispheric asymmetries in hippocampal volume related to memory in left and right temporal variants of frontotemporal degeneration

Front Neurol. 2024 Apr 29:15:1374827. doi: 10.3389/fneur.2024.1374827. eCollection 2024.

Abstract

In addition to Alzheimer's disease (AD), the hippocampus is now known to be affected in variants of frontotemporal degeneration (FTD). In semantic variant primary progressive aphasia (svPPA), characterized by language impairments, hippocampal atrophy is greater in the left hemisphere. Nonverbal impairments (e.g., visual object recognition) are prominent in the right temporal variant of FTD (rtvFTD), and hippocampal atrophy may be greater in the right hemisphere. In this study we examined the hypothesis that leftward hippocampal asymmetry (predicted in svPPA) would be associated with selective verbal memory impairments (with relative preservation of visual memory), while rightward asymmetry (predicted in rtvFTD) would be associated with the opposite pattern (greater visual memory impairment). In contrast, we predicted that controls and individuals in the amnestic mild cognitive impairment stage of AD (aMCI), both of whom were expected to show symmetrical hippocampal volumes, would show roughly equivalent scores in verbal and visual memory. Participants completed delayed recall tests with words and geometric shapes, and hippocampal volumes were assessed with MRI. The aMCI sample showed symmetrical hippocampal atrophy, and similar degree of verbal and visual memory impairment. The svPPA sample showed greater left hippocampal atrophy and verbal memory impairment, while rtvFTD showed greater right hippocampal atrophy and visual memory impairment. Greater asymmetry in hippocampal volumes was associated with larger differences between verbal and visual memory in the FTD samples. Unlike AD, asymmetry is a core feature of brain-memory relationships in temporal variants of FTD.

Keywords: Alzheimer’s disease; episodic memory; frontotemporal dementia; frontotemporal lobar degeneration; hippocampus; primary progressive aphasia; right temporal variant FTD; semantic dementia.

Grants and funding

The author(s) declare financial support was received for the research, authorship, and/or publication of this article. This study was supported by the National Institute on Aging (1P30 AG062428 and 1P30 AG072959), Keep Memory Alive Foundation and The Iversen Family Endowed Chair in Alzheimer’s Disease Research. Additional funding for the control group assessments was provided by a Cleveland State University Faculty Research and Development award to RH.