Four‐Year Follow‐up of [18F]Fluorodeoxyglucose Positron Emission Tomography–Based Parkinson's Disease–Related Pattern Expression in 20 Patients with Isolated Rapid Eye Movement Sleep Behavior Disorder Shows Prodromal Progression
Background Isolated rapid eye movement sleep behavior disorder is known to be prodromal for alpha‐synucleinopathies, such as Parkinson's disease (PD) and dementia with Lewy bodies. The [18F]fluorodeoxyglucose‐positron emission tomography (PET)–based PD‐related brain pattern can be used to monit...
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Published in | Movement disorders Vol. 36; no. 1; pp. 230 - 235 |
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Main Authors | , , , , , , , , , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
Hoboken, USA
John Wiley & Sons, Inc
01.01.2021
Wiley Subscription Services, Inc |
Subjects | |
Online Access | Get full text |
ISSN | 0885-3185 1531-8257 |
DOI | 10.1002/mds.28260 |
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Abstract | Background
Isolated rapid eye movement sleep behavior disorder is known to be prodromal for alpha‐synucleinopathies, such as Parkinson's disease (PD) and dementia with Lewy bodies. The [18F]fluorodeoxyglucose‐positron emission tomography (PET)–based PD‐related brain pattern can be used to monitor disease progression.
Objective
We longitudinally investigated PD‐related brain pattern expression changes in 20 subjects with isolated rapid eye movement sleep behavior disorder to investigate whether this may be a suitable technique to study prodromal PD progression in these patients and to identify potential phenoconverters.
Methods
Subjects underwent two [18F]fluorodeoxyglucose‐PET brain scans ~3.7 years apart, along with baseline and repeated motor, cognitive, and olfactory testing within roughly the same time frame.
Results
At baseline, 8 of 20 (40%) subjects significantly expressed the PD‐related brain pattern (with z scores above the receiver operating characteristic–determined threshold). At follow‐up, six additional subjects exhibited significant PD‐related brain pattern expression (70% in total). PD‐related brain pattern expression increased in all subjects (P = 0.00008). Four subjects (20%), all with significant baseline PD‐related brain pattern expression, phenoconverted to clinical PD.
Conclusions
Suprathreshold PD‐related brain pattern expression and greater score rate of change may signify greater shorter‐term risk for phenoconversion. Our results support the use of serial PD‐related brain pattern expression measurements as a prodromal PD progression biomarker in patients with isolated rapid eye movement sleep behavior disorder. © 2020 The Authors. Movement Disorders published by Wiley Periodicals LLC on behalf of International Parkinson and Movement Disorder Society |
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AbstractList | Isolated rapid eye movement sleep behavior disorder is known to be prodromal for alpha-synucleinopathies, such as Parkinson's disease (PD) and dementia with Lewy bodies. The [
F]fluorodeoxyglucose-positron emission tomography (PET)-based PD-related brain pattern can be used to monitor disease progression.
We longitudinally investigated PD-related brain pattern expression changes in 20 subjects with isolated rapid eye movement sleep behavior disorder to investigate whether this may be a suitable technique to study prodromal PD progression in these patients and to identify potential phenoconverters.
Subjects underwent two [
F]fluorodeoxyglucose-PET brain scans ~3.7 years apart, along with baseline and repeated motor, cognitive, and olfactory testing within roughly the same time frame.
At baseline, 8 of 20 (40%) subjects significantly expressed the PD-related brain pattern (with z scores above the receiver operating characteristic-determined threshold). At follow-up, six additional subjects exhibited significant PD-related brain pattern expression (70% in total). PD-related brain pattern expression increased in all subjects (P = 0.00008). Four subjects (20%), all with significant baseline PD-related brain pattern expression, phenoconverted to clinical PD.
Suprathreshold PD-related brain pattern expression and greater score rate of change may signify greater shorter-term risk for phenoconversion. Our results support the use of serial PD-related brain pattern expression measurements as a prodromal PD progression biomarker in patients with isolated rapid eye movement sleep behavior disorder. © 2020 The Authors. Movement Disorders published by Wiley Periodicals LLC on behalf of International Parkinson and Movement Disorder Society. Background Isolated rapid eye movement sleep behavior disorder is known to be prodromal for alpha‐synucleinopathies, such as Parkinson's disease (PD) and dementia with Lewy bodies. The [18F]fluorodeoxyglucose‐positron emission tomography (PET)–based PD‐related brain pattern can be used to monitor disease progression. Objective We longitudinally investigated PD‐related brain pattern expression changes in 20 subjects with isolated rapid eye movement sleep behavior disorder to investigate whether this may be a suitable technique to study prodromal PD progression in these patients and to identify potential phenoconverters. Methods Subjects underwent two [18F]fluorodeoxyglucose‐PET brain scans ~3.7 years apart, along with baseline and repeated motor, cognitive, and olfactory testing within roughly the same time frame. Results At baseline, 8 of 20 (40%) subjects significantly expressed the PD‐related brain pattern (with z scores above the receiver operating characteristic–determined threshold). At follow‐up, six additional subjects exhibited significant PD‐related brain pattern expression (70% in total). PD‐related brain pattern expression increased in all subjects (P = 0.00008). Four subjects (20%), all with significant baseline PD‐related brain pattern expression, phenoconverted to clinical PD. Conclusions Suprathreshold PD‐related brain pattern expression and greater score rate of change may signify greater shorter‐term risk for phenoconversion. Our results support the use of serial PD‐related brain pattern expression measurements as a prodromal PD progression biomarker in patients with isolated rapid eye movement sleep behavior disorder. © 2020 The Authors. Movement Disorders published by Wiley Periodicals LLC on behalf of International Parkinson and Movement Disorder Society BackgroundIsolated rapid eye movement sleep behavior disorder is known to be prodromal for alpha‐synucleinopathies, such as Parkinson's disease (PD) and dementia with Lewy bodies. The [18F]fluorodeoxyglucose‐positron emission tomography (PET)–based PD‐related brain pattern can be used to monitor disease progression.ObjectiveWe longitudinally investigated PD‐related brain pattern expression changes in 20 subjects with isolated rapid eye movement sleep behavior disorder to investigate whether this may be a suitable technique to study prodromal PD progression in these patients and to identify potential phenoconverters.MethodsSubjects underwent two [18F]fluorodeoxyglucose‐PET brain scans ~3.7 years apart, along with baseline and repeated motor, cognitive, and olfactory testing within roughly the same time frame.ResultsAt baseline, 8 of 20 (40%) subjects significantly expressed the PD‐related brain pattern (with z scores above the receiver operating characteristic–determined threshold). At follow‐up, six additional subjects exhibited significant PD‐related brain pattern expression (70% in total). PD‐related brain pattern expression increased in all subjects (P = 0.00008). Four subjects (20%), all with significant baseline PD‐related brain pattern expression, phenoconverted to clinical PD.ConclusionsSuprathreshold PD‐related brain pattern expression and greater score rate of change may signify greater shorter‐term risk for phenoconversion. Our results support the use of serial PD‐related brain pattern expression measurements as a prodromal PD progression biomarker in patients with isolated rapid eye movement sleep behavior disorder. © 2020 The Authors. Movement Disorders published by Wiley Periodicals LLC on behalf of International Parkinson and Movement Disorder Society |
Author | García, David Vállez Janzen, Annette Peretti, Débora E. Reesink, Fransje E. Oertel, Wolfgang H. Kogan, Rosalie V. Reetz, Kathrin Booij, Jan Kok, Jelmer G. Gurvits, Vita Teune, Laura K. Overeem, Sebastiaan Mayer, Geert Pijpers, Angelique Renken, Remco J. Meles, Sanne K. Sittig, Elisabeth Leenders, Klaus L. Bernhard, Felix |
AuthorAffiliation | 2 Department of Neurology Philipps‐Universität Marburg Marburg Germany 3 Department of Neurology University of Groningen, University Medical Center Groningen Groningen the Netherlands 4 Department of Biomedical Sciences of Cells & Systems, Cognitive Neuroscience Center University of Groningen Groningen the Netherlands 5 Institute for Neurogenomics Helmholtz Center for Health and Environment Munich Germany 1 Department of Nuclear Medicine and Molecular Imaging University of Groningen, University Medical Center Groningen Groningen the Netherlands |
AuthorAffiliation_xml | – name: 5 Institute for Neurogenomics Helmholtz Center for Health and Environment Munich Germany – name: 1 Department of Nuclear Medicine and Molecular Imaging University of Groningen, University Medical Center Groningen Groningen the Netherlands – name: 3 Department of Neurology University of Groningen, University Medical Center Groningen Groningen the Netherlands – name: 2 Department of Neurology Philipps‐Universität Marburg Marburg Germany – name: 4 Department of Biomedical Sciences of Cells & Systems, Cognitive Neuroscience Center University of Groningen Groningen the Netherlands |
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ContentType | Journal Article |
Contributor | Reesink, Fransje E Overeem, Sebastiaan García, David Vállez Peretti, Débora E Pijpers, Angelique Reetz, Kathrin Booij, Jan Bernhard, Felix Teune, Laura K Kok, Jelmer G |
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Copyright | 2020 The Authors. published by Wiley Periodicals LLC on behalf of International Parkinson and Movement Disorder Society 2020 The Authors. Movement Disorders published by Wiley Periodicals LLC on behalf of International Parkinson and Movement Disorder Society. 2020. This article is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. |
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Keywords | Parkinson's disease-related pattern [18F]FDG-PET prodromal progression biomarker neuroimaging rapid eye movement sleep behavior disorder |
Language | English |
License | Attribution 2020 The Authors. Movement Disorders published by Wiley Periodicals LLC on behalf of International Parkinson and Movement Disorder Society. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
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Notes | Full financial disclosures and author roles may be found in the online version of this article. Members of the REMPET Working Group are listed in the Appendix. Rosalie V. Kogan, Annette Janzen, Klaus L. Leenders, and Wolfgang H. Oertel share first and last authorship. Nothing to report. This study was funded by Dutch “Stichting ParkinsonFonds” and the German “ParkinsonFonds Deutschland. The funders of this study did not have any role in designing this study, collecting, analyzing, or interpreting the data, or in writing this article. The corresponding author had access to and responsibility for all of the relevant data that were submitted for publication. Relevant conflicts of interest/financial disclosures Funding agencies ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 14 Funding agencies: This study was funded by Dutch “Stichting ParkinsonFonds” and the German “ParkinsonFonds Deutschland. The funders of this study did not have any role in designing this study, collecting, analyzing, or interpreting the data, or in writing this article. The corresponding author had access to and responsibility for all of the relevant data that were submitted for publication. Relevant conflicts of interest/financial disclosures: Nothing to report. |
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Isolated rapid eye movement sleep behavior disorder is known to be prodromal for alpha‐synucleinopathies, such as Parkinson's disease (PD) and... Isolated rapid eye movement sleep behavior disorder is known to be prodromal for alpha-synucleinopathies, such as Parkinson's disease (PD) and dementia with... BackgroundIsolated rapid eye movement sleep behavior disorder is known to be prodromal for alpha‐synucleinopathies, such as Parkinson's disease (PD) and... |
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SubjectTerms | [18F]FDG‐PET Behavior disorders Brief Report Cognitive ability Dementia disorders Eye movements Follow-Up Studies Humans Lewy bodies Movement disorders Neurodegenerative diseases Neuroimaging Parkinson Disease - diagnostic imaging Parkinson's disease Parkinson's disease–related pattern Positron emission tomography prodromal progression biomarker Prodromal Symptoms rapid eye movement sleep behavior disorder Regular Issue REM sleep REM Sleep Behavior Disorder - diagnostic imaging Sleep Sleep disorders |
Title | Four‐Year Follow‐up of [18F]Fluorodeoxyglucose Positron Emission Tomography–Based Parkinson's Disease–Related Pattern Expression in 20 Patients with Isolated Rapid Eye Movement Sleep Behavior Disorder Shows Prodromal Progression |
URI | https://onlinelibrary.wiley.com/doi/abs/10.1002%2Fmds.28260 https://www.ncbi.nlm.nih.gov/pubmed/32909650 https://www.proquest.com/docview/2480336290 https://pubmed.ncbi.nlm.nih.gov/PMC7891341 |
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