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Clinical Routine FDG-PET Imaging of Suspected Progressive Supranuclear Palsy and Corticobasal Degeneration: A Gatekeeper for Subsequent Tau-PET Imaging?

Background: F-18-fluordeoxyglucose positron emission tomography (FDG-PET) is widely used for discriminative diagnosis of tau-positive atypical parkinsonian syndromes (T+APS). This approach now stands to be augmented with more specific tau tracers. Therefore, we retrospectively analyzed a large clini...

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Autores principales: Beyer, Leonie, Meyer-Wilmes, Johanna, Schönecker, Sonja, Schnabel, Jonas, Brendel, Eva, Prix, Catharina, Nübling, Georg, Unterrainer, Marcus, Albert, Nathalie L., Pogarell, Oliver, Perneczky, Robert, Catak, Cihan, Bürger, Katharina, Bartenstein, Peter, Bötzel, Kai, Levin, Johannes, Rominger, Axel, Brendel, Matthias
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6019471/
https://www.ncbi.nlm.nih.gov/pubmed/29973914
http://dx.doi.org/10.3389/fneur.2018.00483
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author Beyer, Leonie
Meyer-Wilmes, Johanna
Schönecker, Sonja
Schnabel, Jonas
Brendel, Eva
Prix, Catharina
Nübling, Georg
Unterrainer, Marcus
Albert, Nathalie L.
Pogarell, Oliver
Perneczky, Robert
Catak, Cihan
Bürger, Katharina
Bartenstein, Peter
Bötzel, Kai
Levin, Johannes
Rominger, Axel
Brendel, Matthias
author_facet Beyer, Leonie
Meyer-Wilmes, Johanna
Schönecker, Sonja
Schnabel, Jonas
Brendel, Eva
Prix, Catharina
Nübling, Georg
Unterrainer, Marcus
Albert, Nathalie L.
Pogarell, Oliver
Perneczky, Robert
Catak, Cihan
Bürger, Katharina
Bartenstein, Peter
Bötzel, Kai
Levin, Johannes
Rominger, Axel
Brendel, Matthias
author_sort Beyer, Leonie
collection PubMed
description Background: F-18-fluordeoxyglucose positron emission tomography (FDG-PET) is widely used for discriminative diagnosis of tau-positive atypical parkinsonian syndromes (T+APS). This approach now stands to be augmented with more specific tau tracers. Therefore, we retrospectively analyzed a large clinical routine dataset of FDG-PET images for evaluation of the strengths and limitations of stand-alone FDG-PET. Methods: A total of 117 patients (age 68.4 ± 11.1 y) underwent an FDG-PET exam. Patients were followed clinically for a minimum of one year and their final clinical diagnosis was recorded. FDG-PET was rated visually (positive/negative) and categorized as high, moderate or low likelihood of T+APS and other neurodegenerative disorders. We then calculated positive and negative predictive values (PPV/NPV) of FDG-PET readings for the different subgroups relative to their final clinical diagnosis. Results: Suspected diagnoses were confirmed by clinical follow-up (≥1 y) for 62 out of 117 (53%) patients. PPV was excellent when FDG-PET indicated a high likelihood of T+APS in combination with low to moderate likelihood of another neurodegenerative disorder. PPV was distinctly lower when FDG-PET indicated only a moderate likelihood of T+APS or when there was deemed equal likelihood of other neurodegenerative disorder. NPV of FDG-PET with a low likelihood for T+APS was high. Conclusions: FDG-PET has high value in clinical routine evaluation of suspected T+APS, gaining satisfactory differential diagnosis in two thirds of the patients. One third of patients would potentially profit from further evaluation by more specific radioligands, with FDG-PET serving gatekeeper function for the more expensive methods.
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spelling pubmed-60194712018-07-04 Clinical Routine FDG-PET Imaging of Suspected Progressive Supranuclear Palsy and Corticobasal Degeneration: A Gatekeeper for Subsequent Tau-PET Imaging? Beyer, Leonie Meyer-Wilmes, Johanna Schönecker, Sonja Schnabel, Jonas Brendel, Eva Prix, Catharina Nübling, Georg Unterrainer, Marcus Albert, Nathalie L. Pogarell, Oliver Perneczky, Robert Catak, Cihan Bürger, Katharina Bartenstein, Peter Bötzel, Kai Levin, Johannes Rominger, Axel Brendel, Matthias Front Neurol Neurology Background: F-18-fluordeoxyglucose positron emission tomography (FDG-PET) is widely used for discriminative diagnosis of tau-positive atypical parkinsonian syndromes (T+APS). This approach now stands to be augmented with more specific tau tracers. Therefore, we retrospectively analyzed a large clinical routine dataset of FDG-PET images for evaluation of the strengths and limitations of stand-alone FDG-PET. Methods: A total of 117 patients (age 68.4 ± 11.1 y) underwent an FDG-PET exam. Patients were followed clinically for a minimum of one year and their final clinical diagnosis was recorded. FDG-PET was rated visually (positive/negative) and categorized as high, moderate or low likelihood of T+APS and other neurodegenerative disorders. We then calculated positive and negative predictive values (PPV/NPV) of FDG-PET readings for the different subgroups relative to their final clinical diagnosis. Results: Suspected diagnoses were confirmed by clinical follow-up (≥1 y) for 62 out of 117 (53%) patients. PPV was excellent when FDG-PET indicated a high likelihood of T+APS in combination with low to moderate likelihood of another neurodegenerative disorder. PPV was distinctly lower when FDG-PET indicated only a moderate likelihood of T+APS or when there was deemed equal likelihood of other neurodegenerative disorder. NPV of FDG-PET with a low likelihood for T+APS was high. Conclusions: FDG-PET has high value in clinical routine evaluation of suspected T+APS, gaining satisfactory differential diagnosis in two thirds of the patients. One third of patients would potentially profit from further evaluation by more specific radioligands, with FDG-PET serving gatekeeper function for the more expensive methods. Frontiers Media S.A. 2018-06-20 /pmc/articles/PMC6019471/ /pubmed/29973914 http://dx.doi.org/10.3389/fneur.2018.00483 Text en Copyright © 2018 Beyer, Meyer-Wilmes, Schönecker, Schnabel, Brendel, Prix, Nübling, Unterrainer, Albert, Pogarell, Perneczky, Catak, Bürger, Bartenstein, Bötzel, Levin, Rominger and Brendel. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Neurology
Beyer, Leonie
Meyer-Wilmes, Johanna
Schönecker, Sonja
Schnabel, Jonas
Brendel, Eva
Prix, Catharina
Nübling, Georg
Unterrainer, Marcus
Albert, Nathalie L.
Pogarell, Oliver
Perneczky, Robert
Catak, Cihan
Bürger, Katharina
Bartenstein, Peter
Bötzel, Kai
Levin, Johannes
Rominger, Axel
Brendel, Matthias
Clinical Routine FDG-PET Imaging of Suspected Progressive Supranuclear Palsy and Corticobasal Degeneration: A Gatekeeper for Subsequent Tau-PET Imaging?
title Clinical Routine FDG-PET Imaging of Suspected Progressive Supranuclear Palsy and Corticobasal Degeneration: A Gatekeeper for Subsequent Tau-PET Imaging?
title_full Clinical Routine FDG-PET Imaging of Suspected Progressive Supranuclear Palsy and Corticobasal Degeneration: A Gatekeeper for Subsequent Tau-PET Imaging?
title_fullStr Clinical Routine FDG-PET Imaging of Suspected Progressive Supranuclear Palsy and Corticobasal Degeneration: A Gatekeeper for Subsequent Tau-PET Imaging?
title_full_unstemmed Clinical Routine FDG-PET Imaging of Suspected Progressive Supranuclear Palsy and Corticobasal Degeneration: A Gatekeeper for Subsequent Tau-PET Imaging?
title_short Clinical Routine FDG-PET Imaging of Suspected Progressive Supranuclear Palsy and Corticobasal Degeneration: A Gatekeeper for Subsequent Tau-PET Imaging?
title_sort clinical routine fdg-pet imaging of suspected progressive supranuclear palsy and corticobasal degeneration: a gatekeeper for subsequent tau-pet imaging?
topic Neurology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6019471/
https://www.ncbi.nlm.nih.gov/pubmed/29973914
http://dx.doi.org/10.3389/fneur.2018.00483
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