Diagnostic Accuracy of Magnetic Resonance Imaging Measures of Brain Atrophy Across the Spectrum of Progressive Supranuclear Palsy and Corticobasal Degeneration.


Journal

JAMA network open
ISSN: 2574-3805
Titre abrégé: JAMA Netw Open
Pays: United States
ID NLM: 101729235

Informations de publication

Date de publication:
01 04 2022
Historique:
entrez: 29 4 2022
pubmed: 30 4 2022
medline: 4 5 2022
Statut: epublish

Résumé

The accurate diagnosis of progressive supranuclear palsy (PSP) and corticobasal degeneration (CBD) is hampered by imperfect clinical-pathological correlations. To assess and compare the diagnostic value of the magnetic resonance parkinsonism index (MRPI) and other magnetic resonance imaging-based measures of cerebral atrophy to differentiate between PSP, CBD, and other neurodegenerative diseases. This prospective diagnostic study included participants with 4-repeat tauopathies (4RT), PSP, CBD, other neurodegenerative diseases and available MRI who appeared in the University of California, San Francisco, Memory and Aging Center database. Data were collected from October 27, 1994, to September 29, 2019. Data were analyzed from March 1 to September 14, 2021. The main outcome of this study was the neuropathological diagnosis of PSP or CBD. The clinical diagnosis at the time of the MRI acquisition was noted. The imaging measures included the MRPI, cortical thickness, subcortical volumes, including the midbrain, pons, and superior cerebellar peduncle volumes. Multinomial logistic regression models (MLRM) combining different cortical and subcortical regions were defined to discriminate between PSP, CBD, and other pathologies. The areas under the receiver operating characteristic curves (AUROC) and cutoffs were calculated to differentiate between PSP, CBD, and other diseases. Of the 326 included participants, 176 (54%) were male, and the mean (SD) age at MRI was 64.1 (8.0) years. The MRPI showed good diagnostic accuracy for the differentiation between PSP and all other pathologies (accuracy, 87%; AUROC, 0.90; 95% CI, 0.86-0.95) and between 4RT and other pathologies (accuracy, 80%; AUROC, 0.82; 95% CI, 0.76-0.87), but did not allow the discrimination of participants with CBD. Its diagnostic accuracy was lower in the subgroup of patients without the canonical PSP-Richardson syndrome (PSP-RS) or probable corticobasal syndrome (CBS) at MRI. MLRM combining cortical and subcortical measurements showed the highest accuracy for the differentiation between PSP and other pathologies (accuracy, 95%; AUROC, 0.98; 95% CI, 0.97-0.99), CBD and other pathologies (accuracy, 83%; AUROC, 0.86; 95% CI, 0.81-0.91), 4RT and other pathologies (accuracy, 89%; AUROC, 0.94; 95% CI, 0.92-0.97), and PSP and CBD (accuracy, 91%; AUROC, 0.95; 95% CI, 0.91-0.99), even in participants without PSP-RS or CBS at MRI. In this study, the combination of widely available cortical and subcortical measures of atrophy on MRI discriminated between PSP, CBD, and other pathologies and could be used to support the diagnosis of 4RT in clinical practice.

Identifiants

pubmed: 35486397
pii: 2791726
doi: 10.1001/jamanetworkopen.2022.9588
pmc: PMC9055455
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't Research Support, N.I.H., Extramural

Langues

eng

Sous-ensembles de citation

IM

Pagination

e229588

Subventions

Organisme : NIA NIH HHS
ID : K24 AG045333
Pays : United States
Organisme : NIA NIH HHS
ID : K24 AG053435
Pays : United States
Organisme : NIA NIH HHS
ID : P30 AG062422
Pays : United States
Organisme : NIA NIH HHS
ID : P01 AG019724
Pays : United States
Organisme : NIA NIH HHS
ID : K08 AG052648
Pays : United States
Organisme : NIDCD NIH HHS
ID : K24 DC015544
Pays : United States
Organisme : NIA NIH HHS
ID : R01 AG059794
Pays : United States
Organisme : NIA NIH HHS
ID : R01 AG062758
Pays : United States
Organisme : NINDS NIH HHS
ID : RF1 NS050915
Pays : United States

Commentaires et corrections

Type : ErratumIn

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Auteurs

Ignacio Illán-Gala (I)

Sant Pau Memory Unit, Department of Neurology, Hospital de la Santa Creu i Sant Pau, Biomedical Research Institute Sant Pau, Universitat Autònoma de Barcelona, Barcelona, Spain.
Atlantic Fellow for Equity in Brain Health at the University of California, San Francisco, Department of Neurology, University of California, San Francisco.
Centro de Investigación en Red-Enfermedades Neurodegenerativas (CIBERNED), Madrid, Spain.

Salvatore Nigro (S)

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, Lecce, Italy.
Institute of Nanotechnology, National Research Council, Lecce, Italy.

Lawren VandeVrede (L)

Memory and Aging Center, Department of Neurology, University of California, San Francisco.

Neus Falgàs (N)

Atlantic Fellow for Equity in Brain Health at the University of California, San Francisco, Department of Neurology, University of California, San Francisco.
Memory and Aging Center, Department of Neurology, University of California, San Francisco.

Hilary W Heuer (HW)

Memory and Aging Center, Department of Neurology, University of California, San Francisco.

Cèlia Painous (C)

Parkinson's Disease & Movement Disorders Unit, Hospital Clínic, Instituto de Investigaciones Biomédicas August Pi i Sunyer, CIBERNED, European Reference Network for Rare Neurological Diseases, Institut de Neurociències, Universitat de Barcelona, Catalonia, Spain.

Yaroslau Compta (Y)

Parkinson's Disease & Movement Disorders Unit, Hospital Clínic, Instituto de Investigaciones Biomédicas August Pi i Sunyer, CIBERNED, European Reference Network for Rare Neurological Diseases, Institut de Neurociències, Universitat de Barcelona, Catalonia, Spain.

Maria J Martí (MJ)

Parkinson's Disease & Movement Disorders Unit, Hospital Clínic, Instituto de Investigaciones Biomédicas August Pi i Sunyer, CIBERNED, European Reference Network for Rare Neurological Diseases, Institut de Neurociències, Universitat de Barcelona, Catalonia, Spain.

Victor Montal (V)

Sant Pau Memory Unit, Department of Neurology, Hospital de la Santa Creu i Sant Pau, Biomedical Research Institute Sant Pau, Universitat Autònoma de Barcelona, Barcelona, Spain.
Centro de Investigación en Red-Enfermedades Neurodegenerativas (CIBERNED), Madrid, Spain.

Javier Pagonabarraga (J)

Centro de Investigación en Red-Enfermedades Neurodegenerativas (CIBERNED), Madrid, Spain.
Movement Disorders Unit, Sant Pau Hospital and Biomedical Research Institute, Barcelona, Spain.
Universitat Autònoma de Barcelona, Barcelona, Spain.

Jaime Kulisevsky (J)

Centro de Investigación en Red-Enfermedades Neurodegenerativas (CIBERNED), Madrid, Spain.
Movement Disorders Unit, Sant Pau Hospital and Biomedical Research Institute, Barcelona, Spain.
Universitat Autònoma de Barcelona, Barcelona, Spain.

Alberto Lleó (A)

Sant Pau Memory Unit, Department of Neurology, Hospital de la Santa Creu i Sant Pau, Biomedical Research Institute Sant Pau, Universitat Autònoma de Barcelona, Barcelona, Spain.
Centro de Investigación en Red-Enfermedades Neurodegenerativas (CIBERNED), Madrid, Spain.

Juan Fortea (J)

Sant Pau Memory Unit, Department of Neurology, Hospital de la Santa Creu i Sant Pau, Biomedical Research Institute Sant Pau, Universitat Autònoma de Barcelona, Barcelona, Spain.
Centro de Investigación en Red-Enfermedades Neurodegenerativas (CIBERNED), Madrid, Spain.

Giancarlo Logroscino (G)

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, Lecce, Italy.
Department of Basic Medicine, Neuroscience, and Sense Organs, University of Bari Aldo Moro, Bari, Italy.

Andrea Quattrone (A)

Department of Medical and Surgical Sciences, Institute of Neurology, Magna Graecia University, Catanzaro, Italy.

Aldo Quattrone (A)

Neuroimaging Research Unit, Institute of Molecular Bioimaging and Physiology, National Research Council, Catanzaro, Italy.
Neuroimaging Research Unit, Institute of Molecular Bioimaging and Physiology, National Research Council, Catanzaro, Italy.

David C Perry (DC)

Memory and Aging Center, Department of Neurology, University of California, San Francisco.

Maria Luisa Gorno-Tempini (ML)

Memory and Aging Center, Department of Neurology, University of California, San Francisco.

Howard J Rosen (HJ)

Memory and Aging Center, Department of Neurology, University of California, San Francisco.

Lea T Grinberg (LT)

Memory and Aging Center, Department of Neurology, University of California, San Francisco.

Salvatore Spina (S)

Memory and Aging Center, Department of Neurology, University of California, San Francisco.

Renaud La Joie (R)

Memory and Aging Center, Department of Neurology, University of California, San Francisco.

Gil D Rabinovici (GD)

Memory and Aging Center, Department of Neurology, University of California, San Francisco.

Bruce L Miller (BL)

Memory and Aging Center, Department of Neurology, University of California, San Francisco.

Julio C Rojas (JC)

Memory and Aging Center, Department of Neurology, University of California, San Francisco.

William W Seeley (WW)

Memory and Aging Center, Department of Neurology, University of California, San Francisco.

Adam L Boxer (AL)

Memory and Aging Center, Department of Neurology, University of California, San Francisco.

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