4.6 Article

The Evolution of REM Sleep Behavior Disorder in Early Parkinson Disease

Journal

SLEEP
Volume 39, Issue 9, Pages 1737-1742

Publisher

OXFORD UNIV PRESS INC
DOI: 10.5665/sleep.6102

Keywords

REM sleep behavior disorder; REM sleep behavioral events; Parkinson disease; neurodegeneration

Funding

  1. Paracelsus-Elena-Klinik, Kassel, Germany
  2. TEVA Pharma/Lundbeck
  3. GE Healthcare
  4. Hermann and Lilly Schilling Foundation
  5. Boehringer Ingelheim
  6. Licher MT
  7. TEVA
  8. MundiPharm
  9. Teva Pharmaceutical Industries Ltd.
  10. Desitin Pharmaceuticals, GmbH
  11. Michael J. Fox Foundation for Parkinson's Research
  12. EU
  13. Teva Pharmaceutical Industries Ltd
  14. Mundipharm Intern

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Study Objectives: To investigate the development of REM sleep behavior disorder (RBD) and REM sleep behavioral events (RBE) not yet fulfilling diagnostic criteria for RBD as markers for neurodegeneration in a cohort of Parkinson disease (PD) patients between their de novo baseline assessment and two-year follow-up in comparison to healthy controls (HC). Methods: Clinically confirmed PD patients and HC with video-supported polysomnography (vPSG) data at baseline were re-investigated after two years. Diagnostic scoring for RBE and RBD was performed in both groups and related to baseline findings. Results: One hundred thirteen PD patients and 102 healthy controls (HC) were included in the study. Within two years, the overall occurrence of behaviors during REM sleep in PD patients increased from 50% to 63% (P = 0.02). RBD increased from 25% to 43% (P < 0.001). Eleven of 29 (38%) RBE positive PD patients and 10/56 (18%) patients with normal REM sleep at baseline converted to RBD. In HC, the occurrence of any REM behavior increased from 17% to 20% (n.s.). RBD increased from 2% to 4% (n.s.). One of 15 (7%) RBE positive HC and 1/85 (1%) HC with normal REM at baseline converted to RBD. Conclusions: RBD increased significantly in PD patients from the de novo state to two-year follow-up. We propose RBE being named prodromal RBD as it may follow a continuous evolution in PD possibly similar to the spreading of Lewy bodies in PD patients. RBD itself was shown as a robust and stable marker of early PD.

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