4.4 Article

Assessment of self-reported and objective daytime sleepiness in adult-onset myotonic dystrophy type 1

期刊

JOURNAL OF CLINICAL SLEEP MEDICINE
卷 17, 期 12, 页码 2383-2391

出版社

AMER ACAD SLEEP MEDICINE

关键词

myotonic dystrophy type 1; excessive daytime sleepiness; Epworth Sleepiness Scale; Multiple Sleep Latency Test; polysomnography

资金

  1. Telethon-UILDM (Italian Muscular Dystrophy Association) [GUP15004]

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The study highlights the high prevalence of excessive daytime sleepiness in adult-onset myotonic dystrophy type 1 patients, with low concordance between different sleep assessments. Patients with daytime sleepiness had shorter disease duration, better sleep quality, and higher self-reported fatigue.
Study Objectives: Excessive daytime sleepiness (EDS) in myotonic dystrophy type 1 is mostly of central origin but it may coexist with sleep-related breathing disorders. However, there is no consensus on the sleep protocols to be used, assessments vary, and only a minority of patients are regularly tested or are on treatment for EDS. Our study presents data on self-reported and objective EDS in adult-onset myotonic dystrophy type 1. Methods: Sixty-three patients with adult-on set DM1 were subjected to EDS-sleep assessments (polysomnography, Multiple Sleep Latency Test, Epworth Sleepiness Scale). Correlation coefficients were computed to assess the relationship between sleep and sleepiness test results, fatigue, and quality of life. Results: 33% and 48% of patients had EDS based, respectively, on the Epworth Sleepiness Scale and the Multiple Sleep Latency Test, with a low concordance between these tests (k = 0.19). Thirteen patients (20%) displayed 2 or more sleep-onset rapid eye movement periods on Multiple Sleep Latency Test. Patients having EDS by Multiple Sleep Latency Test had a shorter disease duration (P<.05), higher total sleep time and sleep efficiency and lower wake after sleep onset on polysomnography. Patients with self-reported EDS reported significantly higher fatigue score compared with patients without EDS(P<.05). No other difference was found in demographic, clinical, and respiratory features. Conclusions: EDS test results are contradictory, making treatment options difficult. Combining quantitative tests and self-reported scales may facilitate physicians in planning EDS care with patients and families.

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