Baseline characteristics of the North American prodromal Synucleinopathy cohort

Author:

Elliott Jonathan E.12ORCID,Lim Miranda M.23456ORCID,Keil Allison T.1ORCID,Postuma Ronald B.78ORCID,Pelletier Amelie9,Gagnon Jean‐François89ORCID,St. Louis Erik K.10ORCID,Forsberg Leah K.10,Fields Julie A.10ORCID,Huddleston Daniel E.11ORCID,Bliwise Donald L.11ORCID,Avidan Alon Y.12,Howell Michael J.1314ORCID,Schenck Carlos H.13,McLeland Jennifer15,Criswell Susan R.15ORCID,Videnovic Aleksandar1617,During Emmanuel H.1819ORCID,Miglis Mitchell G.1819ORCID,Shprecher David R.20ORCID,Lee‐Iannotti Joyce K.20ORCID,Boeve Bradley F.10ORCID,Ju Yo‐El S.15ORCID,

Affiliation:

1. VA Portland Health Care System Research Service Portland Oregon USA

2. Oregon Health & Science University Neurology, Portland Oregon USA

3. Behavioral Neuroscience Oregon Health & Science University Portland Oregon USA

4. Department of Pulmonary and Critical Care Medicine Oregon Health & Science University Portland Oregon USA

5. Oregon Institute of Occupational Health Sciences Oregon Health & Science University Portland Oregon USA

6. Neurology VA Portland Health Care System Portland Oregon USA

7. Montreal Neurological Institute McGill University Montreal Québec Canada

8. Psychology Université du Québec à Montréal Montreal Québec Canada

9. Hôpital du Sacré‐Coeur de Montréal Center for Advanced Research in Sleep Medicine Montreal Québec Canada

10. Mayo Clinic, Neurology and Medicine Rochester Minnesota USA

11. Neurology Emory University Atlanta Georgia USA

12. Neurology, Sleep Disorders Center University of California Los Angeles Los Angeles California USA

13. Neurology University of Minnesota Medical Center Minneapolis Minnesota USA

14. Hennepin County Medical Center, Minnesota Regional Sleep Disorders Center Minneapolis Minnesota USA

15. Washington University School of Medicine St. Louis Missouri USA

16. Movement Disorders Unit, Division of Sleep Medicine Massachusetts General Hospital Boston Massachusetts USA

17. Harvard Medical School Neurological Clinical Research Institute Boston Massachusetts USA

18. Psychiatry and Behavioral Sciences Stanford University Redwood City California USA

19. Neurology & Neurological Sciences Stanford University Palo Alto California USA

20. Neurology Banner Sun Health Research Institute Phoenix Arizona USA

Abstract

AbstractObjectiveRapid 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.MethodsParticipants ≥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.ResultsOutcomes 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).InterpretationThese 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.

Funder

U.S. Department of Veterans Affairs

Publisher

Wiley

Subject

Neurology (clinical),General Neuroscience

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