Development and Validation of Automated Magnetic Resonance Parkinsonism Index 2.0 to Distinguish Progressive Supranuclear Palsy-Parkinsonism From Parkinson's Disease.


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:
06 2022
Historique:
revised: 21 02 2022
received: 30 12 2021
accepted: 23 02 2022
pubmed: 12 4 2022
medline: 18 6 2022
entrez: 11 4 2022
Statut: ppublish

Résumé

Differentiating progressive supranuclear palsy-parkinsonism (PSP-P) from Parkinson's disease (PD) is clinically challenging. This study aimed to develop an automated Magnetic Resonance Parkinsonism Index 2.0 (MRPI 2.0) algorithm to distinguish PSP-P from PD and to validate its diagnostic performance in two large independent cohorts. We enrolled 676 participants: a training cohort (n = 346; 43 PSP-P, 194 PD, and 109 control subjects) from our center and an independent testing cohort (n = 330; 62 PSP-P, 171 PD, and 97 control subjects) from an international research group. We developed a new in-house algorithm for MRPI 2.0 calculation and assessed its performance in distinguishing PSP-P from PD and control subjects in both cohorts using receiver operating characteristic curves. The automated MRPI 2.0 showed excellent performance in differentiating patients with PSP-P from patients with PD and control subjects both in the training cohort (area under the receiver operating characteristic curve [AUC] = 0.93 [95% confidence interval, 0.89-0.98] and AUC = 0.97 [0.93-1.00], respectively) and in the international testing cohort (PSP-P versus PD, AUC = 0.92 [0.87-0.97]; PSP-P versus controls, AUC = 0.94 [0.90-0.98]), suggesting the generalizability of the results. The automated MRPI 2.0 also accurately distinguished between PSP-P and PD in the early stage of the diseases (AUC = 0.91 [0.84-0.97]). A strong correlation (r = 0.91, P < 0.001) was found between automated and manual MRPI 2.0 values. Our study provides an automated, validated, and generalizable magnetic resonance biomarker to distinguish PSP-P from PD. The use of the automated MRPI 2.0 algorithm rather than manual measurements could be important to standardize measures in patients with PSP-P across centers, with a positive impact on multicenter studies and clinical trials involving patients from different geographic regions. © 2022 The Authors. Movement Disorders published by Wiley Periodicals LLC on behalf of International Parkinson and Movement Disorder Society.

Sections du résumé

BACKGROUND
Differentiating progressive supranuclear palsy-parkinsonism (PSP-P) from Parkinson's disease (PD) is clinically challenging.
OBJECTIVE
This study aimed to develop an automated Magnetic Resonance Parkinsonism Index 2.0 (MRPI 2.0) algorithm to distinguish PSP-P from PD and to validate its diagnostic performance in two large independent cohorts.
METHODS
We enrolled 676 participants: a training cohort (n = 346; 43 PSP-P, 194 PD, and 109 control subjects) from our center and an independent testing cohort (n = 330; 62 PSP-P, 171 PD, and 97 control subjects) from an international research group. We developed a new in-house algorithm for MRPI 2.0 calculation and assessed its performance in distinguishing PSP-P from PD and control subjects in both cohorts using receiver operating characteristic curves.
RESULTS
The automated MRPI 2.0 showed excellent performance in differentiating patients with PSP-P from patients with PD and control subjects both in the training cohort (area under the receiver operating characteristic curve [AUC] = 0.93 [95% confidence interval, 0.89-0.98] and AUC = 0.97 [0.93-1.00], respectively) and in the international testing cohort (PSP-P versus PD, AUC = 0.92 [0.87-0.97]; PSP-P versus controls, AUC = 0.94 [0.90-0.98]), suggesting the generalizability of the results. The automated MRPI 2.0 also accurately distinguished between PSP-P and PD in the early stage of the diseases (AUC = 0.91 [0.84-0.97]). A strong correlation (r = 0.91, P < 0.001) was found between automated and manual MRPI 2.0 values.
CONCLUSIONS
Our study provides an automated, validated, and generalizable magnetic resonance biomarker to distinguish PSP-P from PD. The use of the automated MRPI 2.0 algorithm rather than manual measurements could be important to standardize measures in patients with PSP-P across centers, with a positive impact on multicenter studies and clinical trials involving patients from different geographic regions. © 2022 The Authors. Movement Disorders published by Wiley Periodicals LLC on behalf of International Parkinson and Movement Disorder Society.

Identifiants

pubmed: 35403258
doi: 10.1002/mds.28992
pmc: PMC9321546
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1272-1281

Informations de copyright

© 2022 The Authors. Movement Disorders published by Wiley Periodicals LLC on behalf of International Parkinson and Movement Disorder Society.

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Auteurs

Andrea Quattrone (A)

Institute of Neurology, University "Magna Graecia", Catanzaro, Italy.
Department of Clinical and Movement Neurosciences, UCL Queen Square Institute of Neurology, University College London, London, United Kingdom.

Maria G Bianco (MG)

Department of Medical and Surgical Sciences, University "Magna Graecia", Catanzaro, Italy.
Neuroscience Research Center, University "Magna Graecia", Catanzaro, Italy.

Angelo Antonini (A)

Parkinson and Movement Disorders Unit, Study Center for Neurodegeneration CESNE, 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, Center for NeuroDegenerative Diseases, University of Pisa, Pisa, Italy.

Antonio P Strafella (AP)

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

Gioacchino Tedeschi (G)

Department of Advanced Medical and Surgical Sciences, University of Campania "Luigi Vanvitelli", Naples, Italy.
MRI Research Center SUN-FISM, University of Campania "Luigi Vanvitelli", Naples, Italy.

Alessandro Tessitore (A)

Department of Advanced Medical and Surgical Sciences, University of Campania "Luigi Vanvitelli", Naples, Italy.
MRI Research Center SUN-FISM, University of Campania "Luigi Vanvitelli", Naples, Italy.

Roberto Cilia (R)

Department of Clinical Neurosciences, Fondazione IRCCS Istituto Neurologico Carlo Besta, Parkinson and Movement Disorders Unit, Milan, Italy.

Maurizio Morelli (M)

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

Salvatore Nigro (S)

Institute of Nanotechnology (NANOTEC), National Research Council, Lecce, Italy.
Center for Neurodegenerative Diseases and the Aging Brain, Department of Clinical Research in Neurology, University of Bari Aldo Moro, "Pia Fondazione Cardinale G. Panico", Tricase, Italy.

Basilio Vescio (B)

Institute of Molecular Bioimaging and Physiology, National Research Council (IBFM-CNR), Catanzaro, Italy.

Pier Paolo Arcuri (PP)

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

Rosa De Micco (R)

Department of Advanced Medical and Surgical Sciences, University of Campania "Luigi Vanvitelli", Naples, Italy.
MRI Research Center SUN-FISM, University of Campania "Luigi Vanvitelli", Naples, Italy.

Mario Cirillo (M)

Department of Advanced Medical and Surgical Sciences, University of Campania "Luigi Vanvitelli", Naples, Italy.
MRI Research Center SUN-FISM, University of Campania "Luigi Vanvitelli", Naples, Italy.

Luca Weis (L)

Parkinson and Movement Disorders Unit, Study Center for Neurodegeneration CESNE, Department of Neuroscience, University of Padua, Padua, Italy.

Eleonora Fiorenzato (E)

Department of General Psychology, University of Padua, Padua, Italy.

Roberta Biundo (R)

Department of General Psychology, University of Padua, Padua, 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.
Neuroimaging Core Facility, 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, Center for NeuroDegenerative Diseases, University of Pisa, Pisa, Italy.

Sonia Mazzucchi (S)

Department of Clinical and Experimental Medicine, Center for NeuroDegenerative Diseases, 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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