Muscle atonia index during multiple sleep latency test: A possible marker to differentiate narcolepsy from other hypersomnias.


Journal

Clinical neurophysiology : official journal of the International Federation of Clinical Neurophysiology
ISSN: 1872-8952
Titre abrégé: Clin Neurophysiol
Pays: Netherlands
ID NLM: 100883319

Informations de publication

Date de publication:
05 2023
Historique:
received: 14 10 2022
revised: 15 01 2023
accepted: 23 01 2023
medline: 17 4 2023
pubmed: 5 3 2023
entrez: 4 3 2023
Statut: ppublish

Résumé

The complexity and delay of the diagnosis of narcolepsy require several diagnostic tests and invasive procedures such as lumbar puncture. Our study aimed to determine the changes in muscle tone (atonia index, AI) at different levels of vigilance during the entire multiple sleep latency test (MSLT) and each nap in people with narcolepsy type 1 (NT1) and 2 (NT2) compared with other hypersomnias and its potential diagnostic value. Twenty-nine patients with NT1 (11 M 18F, mean age 34.9 years, SD 16.8) and sixteen with NT2 (10 M 6F, mean age 39 years, SD 11.8) and 20 controls with other hypersomnias (10 M, 10F mean age 45.1 years, SD 15.1) were recruited. AI was evaluated at different levels of vigilance (Wake and REM sleep) in each nap and throughout the MSLT of each group. The validity of AI in identifying patients with narcolepsy (NT1 and NT2) was analyzed using receiver operating characteristic (ROC) curves. AI during wakefulness (WAI) was significantly higher in the narcolepsy groups (NT1 and NT2 p < 0.001) compared to the hypersomniac group. AI during REM sleep (RAI) (p = 0.03) and WAI in nap with sudden onsets of REM sleep periods (SOREMP) (p = 0.001) were lower in NT1 than in NT2. The ROC curves showed high AUC values for WAI (NT1 0.88; Best Cut-off > 0.57, Sensitivity 79.3 % Specificity 90 %; NT2 0.89 Best Cut-off > 0.67 Sensitivity 87.5 % Specificity 95 %; NT1 and NT2 0.88 Best Cut-off > 0.57 Sensitivity 82.2 % Specificity 90 %) in discriminating subjects suffering from other hypersomnias. RAI and WAI in nap with SOREMP showed a poor AUC value (RAI AUC: 0.7 Best cutoff 0.7 Sensitivity 50 % Specificity 87.5 %; WAI in nap before SOREMP AUC: 0.66, Best cut-off < 0.82 sensitivity 61.9 % and specificity 67.35 %) differentiating NT1 and NT2. WAI may represent an encouraging electrophysiological marker of narcolepsy and suggests a vulnerable tendency to dissociative wake / sleep dysregulation lacking in other forms of hypersomnia. AI during wakefulness may help distinguish between narcolepsy and other hypersomnias.

Identifiants

pubmed: 36870217
pii: S1388-2457(23)00185-2
doi: 10.1016/j.clinph.2023.01.019
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

25-31

Informations de copyright

Copyright © 2023 International Federation of Clinical Neurophysiology. Published by Elsevier B.V. All rights reserved.

Auteurs

A Romigi (A)

IRCCS Neuromed Istituto Neurologico Mediterraneo, Sleep Medicine Center, Via Atinense 18, Pozzilli, IS, Italy. Electronic address: andrea.romigi@gmail.com.

M Caccamo (M)

IRCCS Neuromed Istituto Neurologico Mediterraneo, Sleep Medicine Center, Via Atinense 18, Pozzilli, IS, Italy.

F Testa (F)

IRCCS Neuromed Istituto Neurologico Mediterraneo, Sleep Medicine Center, Via Atinense 18, Pozzilli, IS, Italy.

D Ticconi (D)

IRCCS Neuromed Istituto Neurologico Mediterraneo, Sleep Medicine Center, Via Atinense 18, Pozzilli, IS, Italy.

S Cappellano (S)

IRCCS Neuromed Istituto Neurologico Mediterraneo, Sleep Medicine Center, Via Atinense 18, Pozzilli, IS, Italy.

B Di Gioia (B)

IRCCS Neuromed Istituto Neurologico Mediterraneo, Sleep Medicine Center, Via Atinense 18, Pozzilli, IS, Italy.

G Vitrani (G)

IRCCS Neuromed Istituto Neurologico Mediterraneo, Sleep Medicine Center, Via Atinense 18, Pozzilli, IS, Italy.

I Rosenzweig (I)

Sleep Disorders Centre, Guy's and St Thomas' NHS Foundation Trust, London, UK; Sleep and Brain Plasticity Centre, Department of Neuroimaging, Institute of Psychiatry, Psychology and Neuroscience (IoPPN), King's College London, UK.

D Centonze (D)

IRCCS Neuromed Istituto Neurologico Mediterraneo, Sleep Medicine Center, Via Atinense 18, Pozzilli, IS, Italy.

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Classifications MeSH