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Published in: European Journal of Nuclear Medicine and Molecular Imaging 4/2012

Open Access 01-04-2012 | Original Article

Using PET with 18F-AV-45 (florbetapir) to quantify brain amyloid load in a clinical environment

Authors: V. Camus, P. Payoux, L. Barré, B. Desgranges, T. Voisin, C. Tauber, R. La Joie, M. Tafani, C. Hommet, G. Chételat, K. Mondon, V. de La Sayette, J. P. Cottier, E. Beaufils, M. J. Ribeiro, V. Gissot, E. Vierron, J. Vercouillie, B. Vellas, F. Eustache, D. Guilloteau

Published in: European Journal of Nuclear Medicine and Molecular Imaging | Issue 4/2012

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Abstract

Purpose

Positron emission tomography (PET) imaging of brain amyloid load has been suggested as a core biomarker for Alzheimer’s disease (AD). The aim of this study was to test the feasibility of using PET imaging with 18F-AV-45 (florbetapir) in a routine clinical environment to differentiate between patients with mild to moderate AD and mild cognitive impairment (MCI) from normal healthy controls (HC).

Methods

In this study, 46 subjects (20 men and 26 women, mean age of 69.0 ± 7.6 years), including 13 with AD, 12 with MCI and 21 HC subjects, were enrolled from three academic memory clinics. PET images were acquired over a 10-min period 50 min after injection of florbetapir (mean ± SD of radioactivity injected, 259 ± 57 MBq). PET images were assessed visually by two individuals blinded to any clinical information and quantitatively via the standard uptake value ratio (SUVr) in the specific regions of interest, which were defined in relation to the cerebellum as the reference region.

Results

The mean values of SUVr were higher in AD patients (median 1.20, Q1-Q3 1.16-1.30) than in HC subjects (median 1.05, Q1-Q3 1.04-1.08; p = 0.0001) in the overall cortex and all cortical regions (precuneus, anterior and posterior cingulate, and frontal median, temporal, parietal and occipital cortex). The MCI subjects also showed a higher uptake of florbetapir in the posterior cingulate cortex (median 1.06, Q1-Q3 0.97-1.28) compared with HC subjects (median 0.95, Q1-Q3 0.82-1.02; p = 0.03). Qualitative visual assessment of the PET scans showed a sensitivity of 84.6% (95% CI 0.55–0.98) and a specificity of 38.1% (95% CI 0.18–0.62) for discriminating AD patients from HC subjects; however, the quantitative assessment of the global cortex SUVr showed a sensitivity of 92.3% and specificity of 90.5% with a cut-off value of 1.122 (area under the curve 0.894).

Conclusion

These preliminary results suggest that PET with florbetapir is a safe and suitable biomarker for AD that can be used routinely in a clinical environment. However, the low specificity of the visual PET scan assessment could be improved by the use of specific training and automatic or semiautomatic quantification tools.
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Metadata
Title
Using PET with 18F-AV-45 (florbetapir) to quantify brain amyloid load in a clinical environment
Authors
V. Camus
P. Payoux
L. Barré
B. Desgranges
T. Voisin
C. Tauber
R. La Joie
M. Tafani
C. Hommet
G. Chételat
K. Mondon
V. de La Sayette
J. P. Cottier
E. Beaufils
M. J. Ribeiro
V. Gissot
E. Vierron
J. Vercouillie
B. Vellas
F. Eustache
D. Guilloteau
Publication date
01-04-2012
Publisher
Springer-Verlag
Published in
European Journal of Nuclear Medicine and Molecular Imaging / Issue 4/2012
Print ISSN: 1619-7070
Electronic ISSN: 1619-7089
DOI
https://doi.org/10.1007/s00259-011-2021-8

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