Characterization of the sleep disorder of anti-IgLON5 disease.
Actigraphy
Aged
Autoimmune Diseases
/ immunology
Cell Adhesion Molecules, Neuronal
/ immunology
Dexmedetomidine
/ pharmacology
Disease Progression
Female
Humans
Hypnotics and Sedatives
/ pharmacology
Male
Middle Aged
Movement
Parasomnias
/ physiopathology
Polysomnography
REM Sleep Behavior Disorder
/ physiopathology
Sleep Apnea, Obstructive
/ physiopathology
Sleep, Slow-Wave
/ physiology
anti-IgLON5 disease
NREM parasomnia
REM sleep behavior disorder
obstructive sleep apnea
stridor
Journal
Sleep
ISSN: 1550-9109
Titre abrégé: Sleep
Pays: United States
ID NLM: 7809084
Informations de publication
Date de publication:
06 09 2019
06 09 2019
Historique:
received:
02
03
2019
revised:
08
04
2019
pubmed:
15
6
2019
medline:
9
7
2020
entrez:
15
6
2019
Statut:
ppublish
Résumé
To characterize the sleep disorder of anti-IgLON5 disease. We reviewed 27 video-polysomnographies (V-PSG), 6 multiple sleep latency tests (MSLT), 2 videsomnoscopies with dexmedetomidine, and 10 actigraphies recorded during the disease course of five patients. Due to severe sleep architecture abnormalities, we used a novel modified sleep scoring system combining conventional stages with a descriptive approach in which two additional stages were identified: undifferentiated-NREM (UN-NREM) and poorly structured N2 (P-SN2) sleep that were characterized by abnormal motor activation and absence or sparse elements of conventional NREM sleep. Sleep-related vocalizations, movements, behaviors, and respiratory abnormalities were reported by bed-partners. In all patients, NREM sleep onset and sleep reentering after an awakening occurred as UN-NREM (median: 29.8% of total sleep time [TST]) and P-SN2 sleep (14.5% TST) associated with vocalizations and simple and quasi-purposeful movements. Sleep initiation was normalized in one patient with a high dose of steroids, but NREM sleep abnormalities reappeared in subsequent V-PSG. In all patients, if sleep continued uninterrupted, there was a progressive normalization with normal N2 (11.7% TST) and N3 (22.3% TST) sleep but stridor and obstructive apnea emerged. REM sleep behavior disorder (RBD) occurred in four patients. Sleep initiation was also altered in MSLT and dexmedetomidine-induced sleep. Actigraphy showed a 10-fold increase of nocturnal activity compared with controls. Sleep abnormalities remained stable during the disease. The sleep disorder of anti-IgLON5 disease presents as a complex sleep pattern characterized by abnormal sleep initiation with undifferentiated NREM sleep, RBD, periods of normal NREM sleep, stridor, and obstructive apnea.
Identifiants
pubmed: 31198936
pii: 5519031
doi: 10.1093/sleep/zsz133
pii:
doi:
Substances chimiques
Cell Adhesion Molecules, Neuronal
0
Hypnotics and Sedatives
0
IgLON5 protein, human
0
Dexmedetomidine
67VB76HONO
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Informations de copyright
© Sleep Research Society 2019. Published by Oxford University Press on behalf of the Sleep Research Society. All rights reserved. For permissions, please email: journals.permissions@oup.com.