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Baseline characteristics of the North American prodromal Synucleinopathy cohort

Authors :
Jonathan E. Elliott
Miranda M. Lim
Allison T. Keil
Ronald B. Postuma
Amelie Pelletier
Jean‐François Gagnon
Erik K. St. Louis
Leah K. Forsberg
Julie A. Fields
Daniel E. Huddleston
Donald L. Bliwise
Alon Y. Avidan
Michael J. Howell
Carlos H. Schenck
Jennifer McLeland
Susan R. Criswell
Aleksandar Videnovic
Emmanuel H. During
Mitchell G. Miglis
David R. Shprecher
Joyce K. Lee‐Iannotti
Bradley F. Boeve
Yo‐El S. Ju
the North American Prodromal Synucleinopathy (NAPS) Consortium
Source :
Annals of Clinical and Translational Neurology, Vol 10, Iss 4, Pp 520-535 (2023)
Publication Year :
2023
Publisher :
Wiley, 2023.

Abstract

Abstract Objective Rapid eye movement (REM) sleep behavior disorder (RBD) is widely considered a prodromal synucleinopathy, as most with RBD develop overt synucleinopathy within ~10 years. Accordingly, RBD offers an opportunity to test potential treatments at the earliest stages of synucleinopathy. The North American Prodromal Synucleinopathy (NAPS) Consortium has created a multisite RBD participant, primarily clinic‐based cohort to better understand characteristics at diagnosis, and in future work, identify predictors of phenoconversion, develop synucleinopathy biomarkers, and enable early stage clinical trial enrollment. Methods Participants ≥18 years of age with overnight polysomnogram‐confirmed RBD without Parkinson's disease, dementia, multiple system atrophy, or narcolepsy were enrolled from nine sites across North America (8/2018 to 4/2021). Data collection included family/personal history of RBD and standardized assessments of cognitive, motor, sensory, and autonomic function. Results Outcomes are primarily reported based on sex (361 total: n = 295 male, n = 66 female), and secondarily based on history of antidepressant use (n = 200 with, n = 154 without; with correction for sex differences) and based on extent of synucleinopathy burden (n = 56 defined as isolated RBD, n = 305 defined as RBD+ [i.e., exhibiting ≥1 abnormality]). Overall, these participants commonly demonstrated abnormalities in global cognition (MoCA; 38%), motor function (alternate tap test; 48%), sensory (BSIT; 57%), autonomic function (orthostatic hypotension, 38.8%), and anxiety/depression (BAI and PHQ‐9; 39.3% and 31%, respectively). Interpretation These RBD participants, assessed with extensive history, demographic, cognitive, motor, sensory, and autonomic function demonstrated a lack of sex differences and high frequency of concomitant neurological abnormalities. These participants will be valuable for future longitudinal study and neuroprotective clinical trials.

Details

Language :
English
ISSN :
23289503
Volume :
10
Issue :
4
Database :
Directory of Open Access Journals
Journal :
Annals of Clinical and Translational Neurology
Publication Type :
Academic Journal
Accession number :
edsdoj.31d9613c029c455b8349abb5094f206a
Document Type :
article
Full Text :
https://doi.org/10.1002/acn3.51738