The role of pedunculopontine nucleus in isolated REM sleep behavior disorder and REM sleep without atonia.
Adult
Blinking
/ physiology
Cross-Sectional Studies
Electric Stimulation
Electromyography
Female
Humans
Male
Middle Aged
Pedunculopontine Tegmental Nucleus
/ physiopathology
Polysomnography
Prepulse Inhibition
/ physiology
REM Sleep Behavior Disorder
/ physiopathology
REM Sleep Parasomnias
/ physiopathology
Reflex, Startle
/ physiology
Auditory startle reflex
Blink reflex
Prepulse inhibition
REM sleep behavior disorder
REM sleep without atonia
Journal
Parkinsonism & related disorders
ISSN: 1873-5126
Titre abrégé: Parkinsonism Relat Disord
Pays: England
ID NLM: 9513583
Informations de publication
Date de publication:
03 2021
03 2021
Historique:
received:
12
09
2020
revised:
25
01
2021
accepted:
26
01
2021
pubmed:
12
2
2021
medline:
28
12
2021
entrez:
11
2
2021
Statut:
ppublish
Résumé
The aim of this study was to analyze the functions of pedunculopontine nucleus (PPN) in isolated REM sleep behavior disorder (iRBD) and REM sleep without atonia (RSWA) to investigate the role of PPN in dream-enacting motor behaviors in RBD. We evaluated the activity of PPN through the prepulse modulation (PPM) together with other brainstem reflexes to investigate the differences in changes at brainstem. We included nine patients with isolated RSWA and 10 patients with iRBD. For diagnosis, all patients underwent polysomnography. None of the patients had parkinsonism or dementia. We also included 17 healthy participants with similar age and sex. Blink reflex (BR), PPM of BR, recovery excitability of BR, and auditory startle reflex (ASR) were recorded in all participants. There was a prepulse inhibition deficit in iRBD and RSWA groups compared to healthy subjects. The BR-R2 recovery at 200 ms interval was also higher in patients with iRBD and RSWA. In ASR recordings, the response probabilities were higher in the RBD group compared to RSWA and control groups. The PPM was abnormal in both iRBD and RSWA whereas ASR was enhanced in iRBD. We suggest that there are certain similarities and differences in the pathophysiologies of iRBD and RSWA.
Identifiants
pubmed: 33571873
pii: S1353-8020(21)00041-9
doi: 10.1016/j.parkreldis.2021.01.025
pii:
doi:
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
68-73Informations de copyright
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