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Presynaptic Dopaminergic Imaging Characterizes Patients with REM Sleep Behavior Disorder Due to Synucleinopathy
D. Arnaldi, P. Mattioli, S. Raffa, M. Pardini, F. Massa, A. Iranzo, A. Perissinotti, A. Niñerola-Baizán, C. Gaig, M. Serradell, A. Muñoz-Lopetegi, G. Mayà, C. Liguori, M. Fernandes, F. Placidi, A. Chiaravalloti, K. Šonka, P. Dušek, D. Zogala, J....
Jazyk angličtina Země Spojené státy americké
Typ dokumentu časopisecké články, multicentrická studie
Grantová podpora
AG62677
Foundation for the National Institutes of Health
Monument Trust Discovery Award from Parkinson's UK
P50 AG016574
NIA NIH HHS - United States
VEGA 1/0712/22
Slovak Scientific Grant Agency
NS100620
Foundation for the National Institutes of Health
Ministero della Salute
GE Healthcare
AG071754
Foundation for the National Institutes of Health
R34 AG056639
NIA NIH HHS - United States
Mayo Clinic Dorothy and Harry T. Mangurian Jr. Lewy Body Dementia Program
LX22NPO5107
National Institute for Neurological Research
Little Family Foundation
Ministero dell'Università e della Ricerca
U19 AG071754
NIA NIH HHS - United States
AG056639
Foundation for the National Institutes of Health
P30 AG062677
NIA NIH HHS - United States
Ted Turner and Family Foundation
APVV-22-0279
Agentúra na Podporu Výskumu a Vývoja
NU21-04-00535
Czech Ministry of Health
National Institute for Health and Care Research
AG016574
Foundation for the National Institutes of Health
APVV-18-0547
Agentúra na Podporu Výskumu a Vývoja
U01 NS100620
NINDS NIH HHS - United States
PubMed
38466158
DOI
10.1002/ana.26902
Knihovny.cz E-zdroje
- MeSH
- demence s Lewyho tělísky * diagnostické zobrazování MeSH
- dopamin * metabolismus MeSH
- jednofotonová emisní výpočetní tomografie MeSH
- lidé středního věku MeSH
- lidé MeSH
- Parkinsonova nemoc * diagnostické zobrazování komplikace MeSH
- porucha chování v REM spánku * diagnostické zobrazování MeSH
- presynaptická zakončení metabolismus MeSH
- senioři MeSH
- strojové učení * MeSH
- synukleinopatie * diagnostické zobrazování MeSH
- zobrazení dopaminergního systému MeSH
- Check Tag
- lidé středního věku MeSH
- lidé MeSH
- mužské pohlaví MeSH
- senioři MeSH
- ženské pohlaví MeSH
- Publikační typ
- časopisecké články MeSH
- multicentrická studie MeSH
OBJECTIVE: To apply a machine learning analysis to clinical and presynaptic dopaminergic imaging data of patients with rapid eye movement (REM) sleep behavior disorder (RBD) to predict the development of Parkinson disease (PD) and dementia with Lewy bodies (DLB). METHODS: In this multicenter study of the International RBD study group, 173 patients (mean age 70.5 ± 6.3 years, 70.5% males) with polysomnography-confirmed RBD who eventually phenoconverted to overt alpha-synucleinopathy (RBD due to synucleinopathy) were enrolled, and underwent baseline presynaptic dopaminergic imaging and clinical assessment, including motor, cognitive, olfaction, and constipation evaluation. For comparison, 232 RBD non-phenoconvertor patients (67.6 ± 7.1 years, 78.4% males) and 160 controls (68.2 ± 7.2 years, 53.1% males) were enrolled. Imaging and clinical features were analyzed by machine learning to determine predictors of phenoconversion. RESULTS: Machine learning analysis showed that clinical data alone poorly predicted phenoconversion. Presynaptic dopaminergic imaging significantly improved the prediction, especially in combination with clinical data, with 77% sensitivity and 85% specificity in differentiating RBD due to synucleinopathy from non phenoconverted RBD patients, and 85% sensitivity and 86% specificity in discriminating PD-converters from DLB-converters. Quantification of presynaptic dopaminergic imaging showed that an empirical z-score cutoff of -1.0 at the most affected hemisphere putamen characterized RBD due to synucleinopathy patients, while a cutoff of -1.0 at the most affected hemisphere putamen/caudate ratio characterized PD-converters. INTERPRETATION: Clinical data alone poorly predicted phenoconversion in RBD due to synucleinopathy patients. Conversely, presynaptic dopaminergic imaging allows a good prediction of forthcoming phenoconversion diagnosis. This finding may be used in designing future disease-modifying trials. ANN NEUROL 2024;95:1178-1192.
Center of Sleep Medicine Dokkyo Medical University Hospital Tochigi Japan
Clinic of Sleep and Chronomedicine St Hedwig Hospital Berlin Germany
Department of Biomedicine and Prevention University of Rome Tor Vergata Rome Italy
Department of Brain and Behavioral Sciences University of Pavia Pavia Italy
Department of Business and Management LUISS University Rome Italy
Department of Environment and Health Istituto Superiore di Sanità Rome Italy
Department of Neurology Dokkyo Medical University Saitama Medical Center Saitama Japan
Department of Neurology Mayo Clinic Rochester Minnesota USA
Department of Neurology P J Safarik University Kosice Slovak Republic
Department of Neurology University Hospital of L Pasteur Kosice Slovak Republic
Department of Neuroscience University of Genoa Genoa Italy
Department of Neurosciences Biomedicine and Movement Sciences University of Verona Verona Italy
Department of Radiology Mayo Clinic Rochester Minnesota USA
Department of Systems Medicine University of Rome Tor Vergata Rome Italy
Division of Neurology Nuffield Department of Clinical Neurosciences Oxford University Oxford UK
EuroMov Digital Health in Motion Univ Montpellier IMT Mines Ales Montpellier France
Institute of Cognitive Sciences and Technologies Consiglio Nazionale delle Ricerche Rome Italy
IRCCS Istituto delle Scienze Neurologiche di Bologna Bologna Italy
IRCCS Ospedale Policlinico San Martino Genoa Italy
Nuclear Medicine Unit Department of Medical Sciences University of Turin Turin Italy
Nuclear Medicine Unit ICS Maugeri SpA SB IRCCS Pavia Italy
Nuclear Medicine Unit University Hospital of Montpellier Montpellier France
Sleep and Neurology Department Beau Soleil Clinic Montpellier France
Sleep Medicine and Epilepsy Unit IRCCS Mondino Foundation Pavia Italy
Sleep Medicine Center Neurology Unit University Hospital of Rome Tor Vergata Rome Italy
Citace poskytuje Crossref.org
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