Progression trajectories from prodromal to overt synucleinopathies: a longitudinal, multicentric brain [18F]FDG-PET study

The phenoconversion trajectory from idiopathic/isolated Rapid eye movement (REM) sleep behavior disorder (iRBD) towards either Parkinson's Disease (PD) or Dementia with Lewy Bodies (DLB) is currently uncertain. We investigated the capability of baseline brain [<sup>18</sup>F]FDG-PET in differentiating between iRBD patients eventually phenoconverting to PD or DLB, by deriving the denovoPDRBD-related pattern (denovoPDRBD-RP) from 32 de novo PD patients; and the denovoDLBRBD-RP from 30 de novo DLB patients, both with evidence of RBD at diagnosis. To explore [<sup>18</sup>F]FDG-PET phenoconversion trajectories prediction power, we applied these two patterns on a group of 115 iRBD patients followed longitudinally. At follow-up (25.6 ± 17.2 months), 42 iRBD patients progressed through overt alpha-synucleinopathy (21 iRBD-PD and 21 iRBD-DLB converters), while 73 patients remained stable at the last follow-up visit (43.2 ± 27.6 months). At survival analysis, both patterns were significantly associated with the phenoconversion trajectories. Brain [<sup>18</sup>F]FDG-PET is a promising biomarker to study progression trajectories in the alpha-synucleinopathy continuum.

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Publication Details

Journal
npj Parkinson s Disease
Published
2024-10-25
DOI
https://doi.org/10.1038/s41531-024-00813-z
Citations
10
Primary Topic
Parkinson's Disease Mechanisms and Treatments
Type
article
Field-Weighted Citation Impact
3.69

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article

Progression trajectories from prodromal to overt synucleinopathies: a longitudinal, multicentric brain [18F]FDG-PET study

Yu Kyeong Kim, Mariana Fernandes, Matteo Bauckneht, Francesco Famà et al.
10 citations
npj Parkinson s Disease
Parkinson's Disease Mechanisms and Treatments
3.69
article

Progression trajectories from prodromal to overt synucleinopathies: a longitudinal, multicentric brain [18F]FDG-PET study

Yu Kyeong Kim, Mariana Fernandes, Matteo Bauckneht, Francesco Famà, Pietro Mattioli, Andrea Brugnolo, Matteo Spanetta, Ryul Kim, Federico Massa, Agostino Chiaravalloti, Matteo Pardini, Jung Hwan Shin, Dario Arnaldi, Silvia Daniela Morbelli, Beatrice Orso, Claudio Liguori, Fabio Placidi, Jee‐Young Lee, Heejung Kim, Eun Jin Yoon
article en
10 citations

Abstract

The phenoconversion trajectory from idiopathic/isolated Rapid eye movement (REM) sleep behavior disorder (iRBD) towards either Parkinson's Disease (PD) or Dementia with Lewy Bodies (DLB) is currently uncertain. We investigated the capability of baseline brain [<sup>18</sup>F]FDG-PET in differentiating between iRBD patients eventually phenoconverting to PD or DLB, by deriving the denovoPDRBD-related pattern (denovoPDRBD-RP) from 32 de novo PD patients; and the denovoDLBRBD-RP from 30 de novo DLB patients, both with evidence of RBD at diagnosis. To explore [<sup>18</sup>F]FDG-PET phenoconversion trajectories prediction power, we applied these two patterns on a group of 115 iRBD patients followed longitudinally. At follow-up (25.6 ± 17.2 months), 42 iRBD patients progressed through overt alpha-synucleinopathy (21 iRBD-PD and 21 iRBD-DLB converters), while 73 patients remained stable at the last follow-up visit (43.2 ± 27.6 months). At survival analysis, both patterns were significantly associated with the phenoconversion trajectories. Brain [<sup>18</sup>F]FDG-PET is a promising biomarker to study progression trajectories in the alpha-synucleinopathy continuum.

npj Parkinson s DiseaseVol. 10(1)
University of Rome Tor Vergata (IT), Seoul National University (KR), Seoul Metropolitan Government (KR), Istituto Neurologico Mediterraneo (IT), Azienda Ospedaliera Citta' della Salute e della Scienza di Torino (IT), SNUH SMG-SNU Boramae Medical Center (KR), Ospedale Santa Maria (IT), Ospedale Policlinico San Martino (IT), Inha University Hospital (KR), University of Turin (IT), University of Genoa (IT)
European Commission, National Research Foundation, Ministero della Salute, Ministero dell’Istruzione, dell’Università e della Ricerca, National Research Foundation of Korea, Ministry of Science and ICT, South Korea
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Parkinson's Disease Mechanisms and Treatments
3.69
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