Assessment of amyloid β in pathologically confirmed frontotemporal dementia syndromes

Rachel H. Tan*, Jillian J. Kril, Yue Yang, Nicole Tom, John R. Hodges, Victor L. Villemagne, Christopher C. Rowe, Cristian E. Leyton, John B. J. Kwok, Lars M. Ittner, Glenda M. Halliday

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

25 Citations (Scopus)
21 Downloads (Pure)

Abstract

Introduction: The diagnostic utility of in vivo amyloid β (Aβ) imaging to aid in the clinical distinction between frontotemporal dementia (FTD) and Alzheimer's disease remains unclear without data on the prevalence and severity of Aβ in pathologically confirmed FTD syndromes. Methods: Aβ was assessed in 98 autopsy-confirmed FTD and 36 control cases, and the pathological accuracy of 11C-Pittsburgh compound B (PiB)–positron emission tomography imaging was assessed in a subset of FTD cases (n = 15). Results: Aβ was identified in a similar proportion of FTD syndromes and age-matched controls and increases with age. Alzheimer's disease pathology was identified in all cases with high PiB retention and in one case with low PiB retention. We further demonstrate a strong regional correlation between volume fraction of histological Aβ with PiB standard uptake value ratio scaled to the white matter. Discussion: The present study provides a pathologic reference to assist in the interpretation of in vivo assessments in FTD syndromes.

Original languageEnglish
Pages (from-to)10-20
Number of pages11
JournalAlzheimer's and Dementia: Diagnosis, Assessment and Disease Monitoring
Volume9
DOIs
Publication statusPublished - 1 Jan 2017
Externally publishedYes

Bibliographical note

Copyright the Author(s) 2017. Version archived for private and non-commercial use with the permission of the author/s and according to publisher conditions. For further rights please contact the publisher.

Keywords

  • 11C-Pittsburgh compound B
  • Alzheimer's disease
  • Amyloid β
  • Diagnostic
  • Frontotemporal dementia syndromes

Fingerprint Dive into the research topics of 'Assessment of amyloid β in pathologically confirmed frontotemporal dementia syndromes'. Together they form a unique fingerprint.

Cite this