TY - JOUR
T1 - Baseline characteristics of the North American prodromal Synucleinopathy cohort
AU - the North American Prodromal Synucleinopathy (NAPS) Consortium
AU - Elliott, Jonathan E.
AU - Lim, Miranda M.
AU - Keil, Allison T.
AU - Postuma, Ronald B.
AU - Pelletier, Amelie
AU - Gagnon, Jean François
AU - St. Louis, Erik K.
AU - Forsberg, Leah K.
AU - Fields, Julie A.
AU - Huddleston, Daniel E.
AU - Bliwise, Donald L.
AU - Avidan, Alon Y.
AU - Howell, Michael J.
AU - Schenck, Carlos H.
AU - McLeland, Jennifer
AU - Criswell, Susan R.
AU - Videnovic, Aleksandar
AU - During, Emmanuel H.
AU - Miglis, Mitchell G.
AU - Shprecher, David R.
AU - Lee-Iannotti, Joyce K.
AU - Boeve, Bradley F.
AU - Ju, Yo El S.
AU - Ju, Yo El S.
AU - Boeve, Bradley F.
AU - Avidan, Alon Y.
AU - Bliwise, Donald L.
AU - Choudhury, Parichita
AU - Criswell, Susan R.
AU - During, Emmanuel H.
AU - Elliott, Jonathan E.
AU - Fields, Julie A.
AU - Forsberg, Leah K.
AU - Gagnon, Jean François
AU - Howell, Michael J.
AU - Huddleston, Daniel E.
AU - Lee-Iannotti, Joyce K.
AU - Lim, Miranda M.
AU - Miglis, Mitchell G.
AU - Postuma, Ronald B.
AU - Shprecher, David R.
AU - St. Louis, Erik K.
AU - Videnovic, Aleksandar
AU - McLeland, Jennifer
AU - Amudson-Huffmaster, Sommer
AU - Brushaber, Nellie
AU - Chung, Jae Woo
AU - De Kam, Joshua
AU - Ekelmans, Adrian
AU - Keane, Marissa
AU - Keil, Allison T.
AU - Kraft, Ruth
AU - Ligman, Brittany R.
AU - MacKinnon, Colum
AU - Miner-Rose, Daeva
AU - Murphy, Samantha
AU - Pelletier, Amelie
AU - Powers, Katherine L.M.
AU - Stauder, Matthew
AU - Rivera, Adreanne
AU - Sanchez, Sarahmay
AU - Summers, Rebekah
AU - Tiegan, Luke
AU - Timm, Paul
AU - Tucker, Kelsey A.
AU - Tran, Peter
AU - Galasko, Douglas
AU - Mignot, Emmanuel
AU - Schenck, Carlos
N1 - Funding Information:
The authors would like to express their sincere appreciation and gratitude for the participation of our research subjects, and to the entire NAPS consortium. Financial support from NIH grants R34 AG056639, U19 AG071754, P50 AG016574, P30 AG62677; VA RRD 1K2 RX002947; and Canadian support via Research Chair in Cognitive Decline in Pathological Aging.
Publisher Copyright:
© 2023 The Authors. Annals of Clinical and Translational Neurology published by Wiley Periodicals LLC on behalf of American Neurological Association.
PY - 2023/4
Y1 - 2023/4
N2 - 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.
AB - 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.
UR - http://www.scopus.com/inward/record.url?scp=85147511784&partnerID=8YFLogxK
U2 - 10.1002/acn3.51738
DO - 10.1002/acn3.51738
M3 - Article
C2 - 36751940
AN - SCOPUS:85147511784
SN - 2328-9503
VL - 10
SP - 520
EP - 535
JO - Annals of Clinical and Translational Neurology
JF - Annals of Clinical and Translational Neurology
IS - 4
ER -