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Baseline characteristics of the North American prodromal Synucleinopathy cohort.
Elliott, Jonathan E; Lim, Miranda M; Keil, Allison T; Postuma, Ronald B; Pelletier, Amelie; Gagnon, Jean-François; St Louis, Erik K; Forsberg, Leah K; Fields, Julie A; Huddleston, Daniel E; Bliwise, Donald L; Avidan, Alon Y; Howell, Michael J; Schenck, Carlos H; McLeland, Jennifer; Criswell, Susan R; Videnovic, Aleksandar; During, Emmanuel H; Miglis, Mitchell G; Shprecher, David R; Lee-Iannotti, Joyce K; Boeve, Bradley F; Ju, Yo-El S.
Afiliación
  • Elliott JE; VA Portland Health Care System, Research Service, Portland, Oregon, USA.
  • Lim MM; Oregon Health & Science University, Neurology, Portland, Oregon, USA.
  • Keil AT; Oregon Health & Science University, Neurology, Portland, Oregon, USA.
  • Postuma RB; Behavioral Neuroscience, Oregon Health & Science University, Portland, Oregon, USA.
  • Pelletier A; Department of Pulmonary and Critical Care Medicine, Oregon Health & Science University, Portland, Oregon, USA.
  • Gagnon JF; Oregon Institute of Occupational Health Sciences, Oregon Health & Science University, Portland, Oregon, USA.
  • St Louis EK; Neurology, VA Portland Health Care System, Portland, Oregon, USA.
  • Forsberg LK; Mental Illness Research Education and Clinical Center, VA Portland Health Care System, Portland, Oregon, USA.
  • Fields JA; National Center for Rehabilitative Auditory Research, VA Portland Health Care System, Portland, Oregon, USA.
  • Huddleston DE; VA Portland Health Care System, Research Service, Portland, Oregon, USA.
  • Bliwise DL; Montreal Neurological Institute, McGill University, Montreal, Québec, Canada.
  • Avidan AY; Psychology, Université du Québec à Montréal, Montreal, Québec, Canada.
  • Howell MJ; Hôpital du Sacré-Coeur de Montréal, Center for Advanced Research in Sleep Medicine, Montreal, Québec, Canada.
  • Schenck CH; Psychology, Université du Québec à Montréal, Montreal, Québec, Canada.
  • McLeland J; Hôpital du Sacré-Coeur de Montréal, Center for Advanced Research in Sleep Medicine, Montreal, Québec, Canada.
  • Criswell SR; Mayo Clinic, Neurology and Medicine, Rochester, Minnesota, USA.
  • Videnovic A; Mayo Clinic, Neurology and Medicine, Rochester, Minnesota, USA.
  • During EH; Mayo Clinic, Neurology and Medicine, Rochester, Minnesota, USA.
  • Miglis MG; Neurology, Emory University, Atlanta, Georgia, USA.
  • Shprecher DR; Neurology, Emory University, Atlanta, Georgia, USA.
  • Lee-Iannotti JK; Neurology, Sleep Disorders Center, University of California Los Angeles, Los Angeles, California, USA.
  • Boeve BF; Neurology, University of Minnesota Medical Center, Minneapolis, Minnesota, USA.
  • Ju YS; Hennepin County Medical Center, Minnesota Regional Sleep Disorders Center, Minneapolis, Minnesota, USA.
Ann Clin Transl Neurol ; 10(4): 520-535, 2023 04.
Article en En | MEDLINE | ID: mdl-36751940
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.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Enfermedad de Parkinson / Atrofia de Múltiples Sistemas / Enfermedad por Cuerpos de Lewy / Trastorno de la Conducta del Sueño REM / Sinucleinopatías Tipo de estudio: Diagnostic_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Female / Humans / Male Idioma: En Revista: Ann Clin Transl Neurol Año: 2023 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Enfermedad de Parkinson / Atrofia de Múltiples Sistemas / Enfermedad por Cuerpos de Lewy / Trastorno de la Conducta del Sueño REM / Sinucleinopatías Tipo de estudio: Diagnostic_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Female / Humans / Male Idioma: En Revista: Ann Clin Transl Neurol Año: 2023 Tipo del documento: Article País de afiliación: Estados Unidos