A New MRI Measure to Early Differentiate Progressive Supranuclear Palsy From De Novo Parkinson's Disease in Clinical Practice: An International Study.


Journal

Movement disorders : official journal of the Movement Disorder Society
ISSN: 1531-8257
Titre abrégé: Mov Disord
Pays: United States
ID NLM: 8610688

Informations de publication

Date de publication:
03 2021
Historique:
revised: 02 09 2020
received: 08 07 2020
accepted: 12 10 2020
pubmed: 6 11 2020
medline: 28 4 2021
entrez: 5 11 2020
Statut: ppublish

Résumé

Enlargement of the third ventricle has been reported in atypical parkinsonism. We investigated whether the measurement of third ventricle width could distinguish Parkinson's disease (PD) from progressive supranuclear palsy (PSP). We assessed a new MR T1-weighted measurement (third ventricle width/internal skull diameter) in a training cohort of 268 participants (98 PD, 73 PSP, 98 controls from our center) and in a testing cohort of 291 participants (82 de novo PD patients and 133 controls from the Parkinson's Progression Markers Initiative, 76 early-stage PSP from an international research group). PD diagnosis was confirmed after a 4-year follow-up. Diagnostic performance of the third ventricle/internal skull diameter was assessed using receiver operating characteristic curve with bootstrapping; the area under the curve of the training cohort was compared with the area under the curve of the testing cohort using the De Long test. In both cohorts, third ventricle/internal skull diameter values did not differ between PD and controls but were significantly lower in PD than in PSP patients (P < 0.0001). In PD, third ventricle/internal skull diameter values did not change significantly between baseline and follow-up evaluation. Receiver operating characteristic analysis accurately differentiated PD from PSP in the training cohort (area under the curve, 0.94; 95% CI, 91.1-97.6; cutoff, 5.72) and in the testing cohort (area under the curve, 0.91; 95% CI, 87.0-97.0; cutoff,: 5.88), validating the generalizability of the results. Our study provides a new reliable and validated MRI measurement for the early differentiation of PD and PSP. The simplicity and generalizability of this biomarker make it suitable for routine clinical practice and for selection of patients in clinical trials worldwide. © 2020 International Parkinson and Movement Disorder Society.

Sections du résumé

BACKGROUND
Enlargement of the third ventricle has been reported in atypical parkinsonism. We investigated whether the measurement of third ventricle width could distinguish Parkinson's disease (PD) from progressive supranuclear palsy (PSP).
METHODS
We assessed a new MR T1-weighted measurement (third ventricle width/internal skull diameter) in a training cohort of 268 participants (98 PD, 73 PSP, 98 controls from our center) and in a testing cohort of 291 participants (82 de novo PD patients and 133 controls from the Parkinson's Progression Markers Initiative, 76 early-stage PSP from an international research group). PD diagnosis was confirmed after a 4-year follow-up. Diagnostic performance of the third ventricle/internal skull diameter was assessed using receiver operating characteristic curve with bootstrapping; the area under the curve of the training cohort was compared with the area under the curve of the testing cohort using the De Long test.
RESULTS
In both cohorts, third ventricle/internal skull diameter values did not differ between PD and controls but were significantly lower in PD than in PSP patients (P < 0.0001). In PD, third ventricle/internal skull diameter values did not change significantly between baseline and follow-up evaluation. Receiver operating characteristic analysis accurately differentiated PD from PSP in the training cohort (area under the curve, 0.94; 95% CI, 91.1-97.6; cutoff, 5.72) and in the testing cohort (area under the curve, 0.91; 95% CI, 87.0-97.0; cutoff,: 5.88), validating the generalizability of the results.
CONCLUSION
Our study provides a new reliable and validated MRI measurement for the early differentiation of PD and PSP. The simplicity and generalizability of this biomarker make it suitable for routine clinical practice and for selection of patients in clinical trials worldwide. © 2020 International Parkinson and Movement Disorder Society.

Identifiants

pubmed: 33151015
doi: 10.1002/mds.28364
pmc: PMC8330364
mid: NIHMS1726629
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

681-689

Subventions

Organisme : NINDS NIH HHS
ID : R01 NS052318
Pays : United States
Organisme : NINDS NIH HHS
ID : U01 NS102038
Pays : United States

Commentaires et corrections

Type : CommentIn
Type : CommentIn

Informations de copyright

© 2020 International Parkinson and Movement Disorder Society.

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Auteurs

Andrea Quattrone (A)

Institute of Neurology, University "Magna Graecia", Catanzaro, Italy.

Angelo Antonini (A)

Department of Neuroscience, University of Padua, Padua, Italy.

David E Vaillancourt (DE)

Department of Applied Physiology and Kinesiology, University of Florida, Gainesville, Florida, USA.
Department of Neurology and Biomedical Engineering, University of Florida, Gainesville, Florida, USA.

Klaus Seppi (K)

Department of Neurology, Medical University Innsbruck, Innsbruck, Austria.
Neuroimaging Core Facility, Medical University Innsbruck, Innsbruck, Austria.

Roberto Ceravolo (R)

Department of Clinical and Experimental Medicine, Unit of Neurology, University of Pisa, Pisa, Italy.

Antonio P Strafella (AP)

Krembil Research Institute, UHN & Research Imaging Centre, Campbell Family Mental Health Research Institute, CAMH, University of Toronto, Toronto, Ontario, Canada.

Maurizio Morelli (M)

Institute of Neurology, University "Magna Graecia", Catanzaro, Italy.

Salvatore Nigro (S)

Neuroscience Research Center, University "Magna Graecia", Catanzaro, Italy.

Basilio Vescio (B)

Biotecnomed S.C.aR.L, Catanzaro, Italy.

Maria G Bianco (MG)

Department of Health Sciences, Magna Graecia University, Catanzaro, Italy.

Roberta Vasta (R)

Neuroscience Research Center, University "Magna Graecia", Catanzaro, Italy.

Pier Paolo Arcuri (PP)

Department of Radiology, Pugliese-Ciaccio Hospital, Catanzaro, Italy.

Luca Weis (L)

IRCCS San Camillo Hospital, Venice, Italy.

Eleonora Fiorenzato (E)

IRCCS San Camillo Hospital, Venice, Italy.

Roberta Biundo (R)

IRCCS San Camillo Hospital, Venice, Italy.

Roxana G Burciu (RG)

Department of Kinesiology and Applied Physiology, University of Delaware, Newark, Delaware, USA.

Florian Krismer (F)

Department of Neurology, Medical University Innsbruck, Innsbruck, Austria.

Nikolaus R McFarland (NR)

Department of Neurology and Biomedical Engineering, University of Florida, Gainesville, Florida, USA.

Christoph Mueller (C)

Department of Neurology, Medical University Innsbruck, Innsbruck, Austria.

Elke R Gizewski (ER)

Neuroimaging Core Facility, Medical University Innsbruck, Innsbruck, Austria.
Department of Neuroradiology, Medical University Innsbruck, Innsbruck, Austria.

Mirco Cosottini (M)

Department of Translational Research and New Technologies, University of Pisa, Pisa, Italy.

Eleonora Del Prete (E)

Department of Clinical and Experimental Medicine, Unit of Neurology, University of Pisa, Pisa, Italy.

Sonia Mazzucchi (S)

Department of Clinical and Experimental Medicine, Unit of Neurology, University of Pisa, Pisa, Italy.

Aldo Quattrone (A)

Neuroscience Research Center, University "Magna Graecia", Catanzaro, Italy.
Institute of Molecular Bioimaging and Physiology, National Research Council (IBFM-CNR), Catanzaro, Italy.

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