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September 04, 2018; 91 (10) Article

REM behavior disorder predicts motor progression and cognitive decline in Parkinson disease

Gennaro Pagano, Rosa De Micco, Tayyabah Yousaf, Heather Wilson, Avinash Chandra, Marios Politis
First published August 8, 2018, DOI: https://doi.org/10.1212/WNL.0000000000006134
Gennaro Pagano
From the Neurodegeneration Imaging Group, Institute of Psychiatry, Psychology and Neuroscience, King's College London, UK.
MD, MSc, MD
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Rosa De Micco
From the Neurodegeneration Imaging Group, Institute of Psychiatry, Psychology and Neuroscience, King's College London, UK.
MD
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Tayyabah Yousaf
From the Neurodegeneration Imaging Group, Institute of Psychiatry, Psychology and Neuroscience, King's College London, UK.
MSc
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Heather Wilson
From the Neurodegeneration Imaging Group, Institute of Psychiatry, Psychology and Neuroscience, King's College London, UK.
MSc
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Avinash Chandra
From the Neurodegeneration Imaging Group, Institute of Psychiatry, Psychology and Neuroscience, King's College London, UK.
MA
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Marios Politis
From the Neurodegeneration Imaging Group, Institute of Psychiatry, Psychology and Neuroscience, King's College London, UK.
MD, MSc, PhD, FRCP, FEAN
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REM behavior disorder predicts motor progression and cognitive decline in Parkinson disease
Gennaro Pagano, Rosa De Micco, Tayyabah Yousaf, Heather Wilson, Avinash Chandra, Marios Politis
Neurology Sep 2018, 91 (10) e894-e905; DOI: 10.1212/WNL.0000000000006134

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Abstract

Objective To investigate whether REM sleep behavior disorder (RBD) is associated with worse motor and cognitive decline in Parkinson disease (PD)

Methods Four-hundred twenty-one drug-naive patients with early-stage PD and 196 controls without PD were included in this study. All participants underwent a [123I]FP-CIT SPECT scan, CSF assessment, 3-tesla MRI, and thorough clinical assessments.

Results At cross-sectional analyses, patients with PD and probable RBD (PD-RBD) had lower CSF β-amyloid 1–42 (Aβ42) levels and higher total tau to Aβ42 CSF ratio, higher nonmotor symptoms burden, and worse scores on neuropsychological tests of processing speed, visuospatial functioning, and delayed recognition memory compared to patients with PD without RBD. At longitudinal analyses, the presence of RBD was associated with faster motor progression (hazard ratio [HR] = 1.368, 95% confidence Interval [CI] = 1.036–1.806; p = 0.027) and cognitive decline (HR = 1.794, 95% CI = 1.163–2.768; p = 0.008) over 60-month follow-up. The presence of RBD was a predictor for motor progression only in patients with PD who had both low α-synuclein levels and low [123I]FP-CIT uptake in the striatum (HR = 2.091, 95% CI = 1.116–3.918; p = 0.021) and a predictor for cognitive decline only in patients with PD who had both low Aβ42 and low α-synuclein levels (HR = 2.810, 95% CI = 1.462–5.400; p = 0.002). In the population of controls without PD, the presence of RBD was not associated with cognitive decline or any baseline pathologic changes.

Conclusion The presence of RBD in PD is associated with faster motor progression in patients with greater synuclein and dopaminergic pathology, and with higher risk of cognitive decline in patients with greater synuclein and amyloid pathology. Our findings provide an important direction toward understanding phenotypes and their prognosis in PD.

Glossary

Aβ42=
β-amyloid 1–42;
CI=
confidence interval;
DAT=
dopamine transporter;
[123I]FP-CIT=
[123I]-2β-carbomethoxy-3β-(4-iodophenyl)-N-(3-fluoropropyl) nortropane;
H&Y=
Hoehn and Yahr;
HR=
hazard ratio;
MDS-UPDRS=
Movement Disorder Society–sponsored revision of the Unified Parkinson's Disease Rating Scale;
MoCA=
Montreal Cognitive Assessment;
PD=
Parkinson disease;
PPMI=
Parkinson's Progression Markers Initiative;
p-tau181=
tau phosphorylated at Thr181;
RBD=
REM sleep behavior disorder;
RBDSQ=
REM Sleep Behavior Disorder Screening Questionnaire;
SBR=
specific binding ratio;
SCOPA-AUT=
Scales for Outcomes in Parkinson’s Disease–Autonomic;
STAI=
State-Trait Anxiety Inventory;
t-tau=
total tau;
UPSIT=
University of Pennsylvania Smell Identification Test;
VOI=
volume of interest

Footnotes

  • Go to Neurology.org/N for full disclosures. Funding information and disclosures deemed relevant by the authors, if any, are provided at the end of the article.

  • Editorial page 435

  • CME Course: NPub.org/cmelist

  • Received February 19, 2018.
  • Accepted in final form May 1, 2018.
  • © 2018 American Academy of Neurology
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