Pierre Payoux

Prof. Pierre Payoux

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Research Focus & Metrics

Academic Career Length

25Years (2002-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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1 May 2017 in The Lancet Neurology
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Journal Article
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SASandrine Andrieu
Sandrine Andrieu
SGSophie Guyonnet
Sophie Guyonnet
NCNicola Coley
Nicola Coley
CCChristelle Cantet
Christelle Cantet
MBMarc Bonnefoy
Marc Bonnefoy
POPascale Olivier-Abbal
Pascale Olivier-Abbal

1 November 2007 in Headache: The Journal of Head and Face Pain
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Journal Article
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MDMarie Denuelle
Marie Denuelle
NFNelly Fabre
Nelly Fabre
PPPierre Payoux
Pierre Payoux
FCFrancois Chollet
Francois Chollet
GGGilles Geraud
Gilles Geraud

2 August 2005 in Movement Disorders
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CBChristine Brefel‐Courbon
Christine Brefel‐Courbon
PPPierre Payoux
Pierre Payoux
CTClaire Thalamas
Claire Thalamas
FOFabienne Ory
Fabienne Ory
IQIsabelle Quelven
Isabelle Quelven
OROlivier Rascol
Olivier Rascol

24 March 2003 in Annals of Neurology
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OROlivier Rascol
Olivier Rascol
PPPierre Payoux
Pierre Payoux
FOFabienne Ory
Fabienne Ory
Joaquim FerreiraJoaquim Ferreira
Joaquim Ferreira
CBChristine Brefel-Courbon
Christine Brefel-Courbon
JMJean-Louis Montastruc
Jean-Louis Montastruc

18 January 2012 in European Journal of Nuclear Medicine and Molecular Imaging
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Journal Article
Open access
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VCV. Camus
V. Camus
PPPierre Payoux
Pierre Payoux
LBL. Barré
L. Barré
BDB. Desgranges
B. Desgranges
TVT. Voisin
T. Voisin
DGD. Guilloteau
D. Guilloteau
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.

1 December 2013 in NeuroImage
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Journal Article
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JJJorge Jovicich
Jorge Jovicich
MMMoira Marizzoni
Moira Marizzoni
RSRoser Sala-Llonch
Roser Sala-Llonch
BBBeatriz Bosch
Beatriz Bosch
DBDavid Bartrés-Faz
David Bartrés-Faz
GFGiovanni B. Frisoni
Giovanni B. Frisoni