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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Frontiers Media S.A.
2018-06-01
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Series: | Frontiers in Neurology |
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Online Access: | https://www.frontiersin.org/article/10.3389/fneur.2018.00483/full |
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record_format |
Article |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Leonie Beyer Johanna Meyer-Wilmes Sonja Schönecker Jonas Schnabel Eva Brendel Catharina Prix Georg Nübling Marcus Unterrainer Nathalie L. Albert Oliver Pogarell Robert Perneczky Robert Perneczky Robert Perneczky Robert Perneczky Cihan Catak Katharina Bürger Katharina Bürger Peter Bartenstein Peter Bartenstein Kai Bötzel Johannes Levin Johannes Levin Axel Rominger Axel Rominger Axel Rominger Matthias Brendel Matthias Brendel |
spellingShingle |
Leonie Beyer Johanna Meyer-Wilmes Sonja Schönecker Jonas Schnabel Eva Brendel Catharina Prix Georg Nübling Marcus Unterrainer Nathalie L. Albert Oliver Pogarell Robert Perneczky Robert Perneczky Robert Perneczky Robert Perneczky Cihan Catak Katharina Bürger Katharina Bürger Peter Bartenstein Peter Bartenstein Kai Bötzel Johannes Levin Johannes Levin Axel Rominger Axel Rominger Axel Rominger Matthias Brendel Matthias Brendel Clinical Routine FDG-PET Imaging of Suspected Progressive Supranuclear Palsy and Corticobasal Degeneration: A Gatekeeper for Subsequent Tau-PET Imaging? Frontiers in Neurology atypical parkinsonian syndrome progressive supranuclear palsy corticobasal degeneration F-18-FDG PET clinical routine |
author_facet |
Leonie Beyer Johanna Meyer-Wilmes Sonja Schönecker Jonas Schnabel Eva Brendel Catharina Prix Georg Nübling Marcus Unterrainer Nathalie L. Albert Oliver Pogarell Robert Perneczky Robert Perneczky Robert Perneczky Robert Perneczky Cihan Catak Katharina Bürger Katharina Bürger Peter Bartenstein Peter Bartenstein Kai Bötzel Johannes Levin Johannes Levin Axel Rominger Axel Rominger Axel Rominger Matthias Brendel Matthias Brendel |
author_sort |
Leonie Beyer |
title |
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_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_sort |
clinical routine fdg-pet imaging of suspected progressive supranuclear palsy and corticobasal degeneration: a gatekeeper for subsequent tau-pet imaging? |
publisher |
Frontiers Media S.A. |
series |
Frontiers in Neurology |
issn |
1664-2295 |
publishDate |
2018-06-01 |
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. |
topic |
atypical parkinsonian syndrome progressive supranuclear palsy corticobasal degeneration F-18-FDG PET clinical routine |
url |
https://www.frontiersin.org/article/10.3389/fneur.2018.00483/full |
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doaj-fd5955cc9a2c479e81d2f41f50e5943d2020-11-24T23:07:49ZengFrontiers Media S.A.Frontiers in Neurology1664-22952018-06-01910.3389/fneur.2018.00483355042Clinical Routine FDG-PET Imaging of Suspected Progressive Supranuclear Palsy and Corticobasal Degeneration: A Gatekeeper for Subsequent Tau-PET Imaging?Leonie Beyer0Johanna Meyer-Wilmes1Sonja Schönecker2Jonas Schnabel3Eva Brendel4Catharina Prix5Georg Nübling6Marcus Unterrainer7Nathalie L. Albert8Oliver Pogarell9Robert Perneczky10Robert Perneczky11Robert Perneczky12Robert Perneczky13Cihan Catak14Katharina Bürger15Katharina Bürger16Peter Bartenstein17Peter Bartenstein18Kai Bötzel19Johannes Levin20Johannes Levin21Axel Rominger22Axel Rominger23Axel Rominger24Matthias Brendel25Matthias Brendel26Department of Nuclear Medicine, University Hospital, LMU Munich, Munich, GermanyDepartment of Nuclear Medicine, University Hospital, LMU Munich, Munich, GermanyDepartment of Neurology, University Hospital, LMU Munich, Munich, GermanyDepartment of Nuclear Medicine, University Hospital, LMU Munich, Munich, GermanyDepartment of Nuclear Medicine, University Hospital, LMU Munich, Munich, GermanyDepartment of Neurology, University Hospital, LMU Munich, Munich, GermanyDepartment of Neurology, University Hospital, LMU Munich, Munich, GermanyDepartment of Nuclear Medicine, University Hospital, LMU Munich, Munich, GermanyDepartment of Nuclear Medicine, University Hospital, LMU Munich, Munich, GermanyDepartment of Psychiatry, University of Munich, Munich, GermanyDepartment of Psychiatry, University of Munich, Munich, GermanyGerman Center for Neurodegenerative Diseases (DZNE), Munich, GermanyNeuroepidemiology and Ageing Research Unit, School of Public Health, Imperial College, London, United KingdomWest London Mental Health NHS Trust, London, United KingdomInstitute for Stroke and Dementia Research, University of Munich, Munich, GermanyGerman Center for Neurodegenerative Diseases (DZNE), Munich, GermanyInstitute for Stroke and Dementia Research, University of Munich, Munich, GermanyDepartment of Nuclear Medicine, University Hospital, LMU Munich, Munich, GermanyMunich Cluster for Systems Neurology (SyNergy), Munich, GermanyDepartment of Neurology, University Hospital, LMU Munich, Munich, GermanyDepartment of Neurology, University Hospital, LMU Munich, Munich, GermanyGerman Center for Neurodegenerative Diseases (DZNE), Munich, GermanyDepartment of Nuclear Medicine, University Hospital, LMU Munich, Munich, GermanyMunich Cluster for Systems Neurology (SyNergy), Munich, GermanyDepartment of Nuclear Medicine, Inselspital, University Hospital Bern, Bern, SwitzerlandDepartment of Nuclear Medicine, University Hospital, LMU Munich, Munich, GermanyMunich Cluster for Systems Neurology (SyNergy), Munich, GermanyBackground: 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.https://www.frontiersin.org/article/10.3389/fneur.2018.00483/fullatypical parkinsonian syndromeprogressive supranuclear palsycorticobasal degenerationF-18-FDGPETclinical routine |