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The hippocampal longitudinal axis – relevance for underlying tau and TDP-43 pathology?

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  • Accepted manuscript

    Accepted author manuscript, 1 MB, PDF-document

    Embargo ends: 1/06/19

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Authors

  • Albert Llado
  • Adrià Tort-Merino
  • Raquel Sanchez-Valle
  • Neus Falgas
  • Mircea Balasa
  • Bea Bosch
  • Magda Castellvi
  • Jaume Olives
  • Anna Antonell
  • Michael Hornberger

Organisational units

Abstract

Recent studies suggest that hippocampus has different cortical connectivity and functionality along its longitudinal axis. We sought to elucidate the possible different pattern of atrophy in longitudinal axis of hippocampus between Amyloid/Tau pathology and TDP-43-pathies.

Seventy-three presenile subjects were included: Amyloid/Tau group (33 Alzheimer’s disease (AD) with confirmed CSF biomarkers), probable TDP-43 group (7 semantic variant progressive primary aphasia, 5 GRN and 2 C9orf72 mutation carriers) and 26 healthy controls. We conducted a region-of-interest voxel-based morphometry analysis on the hippocampal longitudinal axis, by contrasting the groups, covarying with CSF biomarkers (Aβ42, total tau, p-tau) and covarying with episodic memory scores. Amyloid/Tau pathology affected mainly posterior hippocampus while anterior left hippocampus was more atrophied in probable TDP-43pathies. We also observed a significant correlation of posterior hippocampal atrophy with AD CSF biomarkers and visual memory scores. Taken together, these data suggest that there is a potential differentiation along the hippocampal longitudinal axis based on the underlying pathology, which could be used as a potential biomarker to identify the underlying pathology in different neurodegenerative diseases.

Details

Original languageEnglish
Pages (from-to)1-9
JournalNeurobiology of Aging
Volume73
Early online date1 Jun 2018
DOIs
Publication statusPublished - Oct 2018
Peer-reviewedYes

Keywords

    Research areas

  • Alzheimer’s disease, tau, TDP-43, MRI, semantic variant of progressive primary aphasia, frontotemporal dementia, memory, hippocampus

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