Optimizing Parkinson’s disease diagnosis: the role of a dual nuclear imaging algorithm

Abstract The diagnosis of Parkinson’s disease (PD) currently relies almost exclusively on the clinical judgment of an experienced neurologist, ideally a specialist in movement disorders. However, such clinical diagnosis is often incorrect in a large percentage of patients, particularly in the early...

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Autores principales: J. William Langston, Jesse C. Wiley, Michele Tagliati
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Lenguaje:EN
Publicado: Nature Portfolio 2018
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Acceso en línea:https://doaj.org/article/1b8e167263ed4d5483547bc741ca5407
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spelling oai:doaj.org-article:1b8e167263ed4d5483547bc741ca54072021-12-02T15:10:33ZOptimizing Parkinson’s disease diagnosis: the role of a dual nuclear imaging algorithm10.1038/s41531-018-0041-92373-8057https://doaj.org/article/1b8e167263ed4d5483547bc741ca54072018-02-01T00:00:00Zhttps://doi.org/10.1038/s41531-018-0041-9https://doaj.org/toc/2373-8057Abstract The diagnosis of Parkinson’s disease (PD) currently relies almost exclusively on the clinical judgment of an experienced neurologist, ideally a specialist in movement disorders. However, such clinical diagnosis is often incorrect in a large percentage of patients, particularly in the early stages of the disease. A commercially available, objective and quantitative marker of nigrostriatal neurodegeneration was recently provided by 123-iodine 123I-ioflupane SPECT imaging, which is however unable to differentiate PD from a variety of other parkinsonian syndromes associated with striatal dopamine deficiency. There is evidence to support an algorithm utilizing a dual neuroimaging strategy combining 123I-ioflupane SPECT and the noradrenergic receptor ligand 123I-metaiodobenzylguanidine (MIBG), which assesses the post-ganglion peripheral autonomic nervous system. Evolving concepts regarding the synucleinopathy affecting the central and peripheral autonomic nervous systems as part of a multisystem disease are reviewed to sustain such strategy. Data are presented to show how MIBG deficits are a common feature of multisystem Lewy body disease and can be used as a unique feature to distinguish PD from atypical parkinsonisms. We propose that the combination of cardiac (MIBG) and cerebral 123I-ioflupane SPECT could satisfy one of the most significant unmet needs of current PD diagnosis and management, namely the early and accurate diagnosis of patients with typical Lewy body PD. Exemplary case scenarios will be described, highlighting how dual neuroimaging strategy can maximize diagnostic accuracy for patient care, clinical trials, pre-symptomatic PD screening, and special cases provided by specific genetic mutations associated with PD.J. William LangstonJesse C. WileyMichele TagliatiNature PortfolioarticleNeurology. Diseases of the nervous systemRC346-429ENnpj Parkinson's Disease, Vol 4, Iss 1, Pp 1-7 (2018)
institution DOAJ
collection DOAJ
language EN
topic Neurology. Diseases of the nervous system
RC346-429
spellingShingle Neurology. Diseases of the nervous system
RC346-429
J. William Langston
Jesse C. Wiley
Michele Tagliati
Optimizing Parkinson’s disease diagnosis: the role of a dual nuclear imaging algorithm
description Abstract The diagnosis of Parkinson’s disease (PD) currently relies almost exclusively on the clinical judgment of an experienced neurologist, ideally a specialist in movement disorders. However, such clinical diagnosis is often incorrect in a large percentage of patients, particularly in the early stages of the disease. A commercially available, objective and quantitative marker of nigrostriatal neurodegeneration was recently provided by 123-iodine 123I-ioflupane SPECT imaging, which is however unable to differentiate PD from a variety of other parkinsonian syndromes associated with striatal dopamine deficiency. There is evidence to support an algorithm utilizing a dual neuroimaging strategy combining 123I-ioflupane SPECT and the noradrenergic receptor ligand 123I-metaiodobenzylguanidine (MIBG), which assesses the post-ganglion peripheral autonomic nervous system. Evolving concepts regarding the synucleinopathy affecting the central and peripheral autonomic nervous systems as part of a multisystem disease are reviewed to sustain such strategy. Data are presented to show how MIBG deficits are a common feature of multisystem Lewy body disease and can be used as a unique feature to distinguish PD from atypical parkinsonisms. We propose that the combination of cardiac (MIBG) and cerebral 123I-ioflupane SPECT could satisfy one of the most significant unmet needs of current PD diagnosis and management, namely the early and accurate diagnosis of patients with typical Lewy body PD. Exemplary case scenarios will be described, highlighting how dual neuroimaging strategy can maximize diagnostic accuracy for patient care, clinical trials, pre-symptomatic PD screening, and special cases provided by specific genetic mutations associated with PD.
format article
author J. William Langston
Jesse C. Wiley
Michele Tagliati
author_facet J. William Langston
Jesse C. Wiley
Michele Tagliati
author_sort J. William Langston
title Optimizing Parkinson’s disease diagnosis: the role of a dual nuclear imaging algorithm
title_short Optimizing Parkinson’s disease diagnosis: the role of a dual nuclear imaging algorithm
title_full Optimizing Parkinson’s disease diagnosis: the role of a dual nuclear imaging algorithm
title_fullStr Optimizing Parkinson’s disease diagnosis: the role of a dual nuclear imaging algorithm
title_full_unstemmed Optimizing Parkinson’s disease diagnosis: the role of a dual nuclear imaging algorithm
title_sort optimizing parkinson’s disease diagnosis: the role of a dual nuclear imaging algorithm
publisher Nature Portfolio
publishDate 2018
url https://doaj.org/article/1b8e167263ed4d5483547bc741ca5407
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AT jessecwiley optimizingparkinsonsdiseasediagnosistheroleofadualnuclearimagingalgorithm
AT micheletagliati optimizingparkinsonsdiseasediagnosistheroleofadualnuclearimagingalgorithm
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