In April 2016 Manchester eScholar was replaced by the University of Manchester’s new Research Information Management System, Pure. In the autumn the University’s research outputs will be available to search and browse via a new Research Portal. Until then the University’s full publication record can be accessed via a temporary portal and the old eScholar content is available to search and browse via this archive.

18F-florbetapir positron emission tomography in patients with frontotemporal dementia and Alzheimer's disease

Kobylecki, C; Langheinrich, T; Hinz, R; Vardy, E; Brown, G; Martino, M; Haense, C; Richardson, A; Gerhard, A; Anton-Rodriguez, J; Snowden, J; Neary, D; Pontecorvo, M; Herholz, K

J Nucl Med. 2015;.

Access to files

Full-text and supplementary files are not available from Manchester eScholar. Full-text is available externally using the following links:

Full-text held externally

Abstract

Pathological deposition of amyloid beta (Abeta) protein is a key component in the pathogenesis of Alzheimer's disease (AD), but not a feature of frontotemporal dementia (FTD). PET ligands for Abeta protein are increasingly used in diagnosis and research of dementia syndromes. Here we report a PET study using 18F-florbetapir in healthy control subjects and patients with AD and FTD. METHODS: Ten healthy controls (mean age 62.5+/-5.2 years), 10 AD patients (mean age 62.6+/-4.5) and 8 FTD patients (mean age 62.5+/-9.6) were recruited to the study. All patients underwent detailed clinical and neuropsychological assessment, T1-weighted MR, and were genotyped for apolipoprotein E (APOE) status. All participants underwent dynamic 18F-florbetapir PET on a high-resolution research tomograph, and FTD patients also underwent FDG PET scans. Standardised uptake value ratios (SUVRs) were extracted for predefined grey and white matter regions of interest using cerebellar grey matter as reference region. Static PET images were evaluated by trained raters blinded to clinical status and regional analysis. RESULTS: Total cortical grey matter florbetapir uptake values were significantly higher in AD (median SUVR 1.73) compared to FTD patients (1.13, P = 0.002) and controls (1.26, P = 0.04). Florbetapir uptake was also higher in AD compared to FTD and controls in frontal, parietal, occipital and cingulate cortex as well as central subcortical regions. Only one FTD patient (homozygous for APOE 4) displayed high cortical florbetapir retention, while FDG PET demonstrated mesiofrontal hypometabolism consistent with the clinical diagnosis of FTD. The majority of visual raters classified 1 control (10%), 8 AD (80%), and 2 FTD (25%) patients as amyloid positive, while ratings were tied in another 2 FTD patients and 1 healthy control. CONCLUSION: Cortical 18F-florbetapir uptake is low in the majority of FTD patients, providing good discrimination from AD. However, visual rating of FTD scans was challenging with a higher rate of discordance between readers than in AD and control subjects.

Bibliographic metadata

Type of resource:
Content type:
Published date:
Language:
eng
Journal title:
Alternative journal title:
Journal of nuclear medicine : official publication, Society of Nuclear Medicine
Digital Object Identifier:
10.2967/jnumed.114.147454
ISI Accession Number:
25655625
General notes:
  • Kobylecki, Christopher Langheinrich, Tobias Hinz, Rainer Vardy, Emma Brown, Gavin Martino, Maria Haense, Cathleen Richardson, Anna Gerhard, Alexander Anton-Rodriguez, Jose Snowden, Julie Neary, David Pontecorvo, Michael Herholz, Karl J Nucl Med. 2015 Feb 5. pii: jnumed.114.147454.
Access state:
Active

Institutional metadata

University researcher(s):

Record metadata

Manchester eScholar ID:
uk-ac-man-scw:269221
Created by:
Gerhard, Alexander
Created:
22nd July, 2015, 10:39:43
Last modified by:
Gerhard, Alexander
Last modified:
16th December, 2015, 08:48:12

Can we help?

The library chat service will be available from 11am-3pm Monday to Friday (excluding Bank Holidays). You can also email your enquiry to us.