Skip to main navigation Skip to search Skip to main content

Retrosplenial cortex (BA 29) volumes in behavioral variant frontotemporal dementia and alzheimer's disease

Rachel H. Tan, Stephanie Wong, John R. Hodges, Glenda M. Halliday, Michael Hornberger*

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

Abstract

Background: The retrosplenial cortex (RSC) is a crucial transit region between the hippocampus and cingulate cortex and has been implicated in spatial navigation and memory. Importantly, RSC atrophy is a predilection site of Alzheimer's (AD) pathology, but there have been no studies assessing structural changes in the RSC in behavioral variant frontotemporal dementia (bvFTD). Methods: A manual tracing method was used to calculate regional RSC volume in MRI scans from patients with bvFTD (n = 15) and AD (n = 15), as well as age- and sex-matched controls (n = 15). Results: RSC volumes were significantly reduced in the AD (p < 0.001), but not the bvFTD cohort (p > 0.1) compared to age-matched controls. RSC volumes discriminated bvFTD from AD in over 90% of the cases. Conclusion: These findings provide further evidence that RSC atrophy is specific to AD, which might explain the commonly observed spatial disorientation in this patient group.

Original languageEnglish
Pages (from-to)177-182
Number of pages6
JournalDementia and Geriatric Cognitive Disorders
Volume35
Issue number3-4
DOIs
Publication statusPublished - Mar 2013
Externally publishedYes

Keywords

  • Alzheimer's disease
  • BA29
  • Behavioral variant frontotemporal dementia
  • Retrosplenial cortex
  • Volumetric tracing

Fingerprint

Dive into the research topics of 'Retrosplenial cortex (BA 29) volumes in behavioral variant frontotemporal dementia and alzheimer's disease'. Together they form a unique fingerprint.

Cite this