Evaluation of Sleep Structure and Sleep-related Disorders in Pediatric Patients Diagnosed with Duchenne Muscular Dystrophy and Spinal Muscular Atrophy

Objective:Duchenne muscular dystrophy (DMD) is a hereditary neuromuscular disorder in which respiratory problems arise secondary to the involvement of skeletal muscles. Spinal muscular atrophy (SMA) is a disorder group characterized by the involvement of anterior horn cells. The most common respirat...

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Main Authors: Nuran Burcu Arkalı, Gülçin Benbir Şenel, Hüseyin Kılıç, Gündüz İncesu, Sema Saltık, Cengiz Yalçınkaya, Derya Karadeniz
Format: Article
Language:English
Published: Galenos Yayinevi 2020-03-01
Series:Türk Uyku Tıbbı Dergisi
Subjects:
Online Access: http://jtsm.org/archives/archive-detail/article-preview/evaluation-of-sleep-structure-and-sleep-related-di/36138
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spelling doaj-9b054a3bb9fd4ad1a1f4c46c1b2a28c22020-11-25T03:06:04ZengGalenos YayineviTürk Uyku Tıbbı Dergisi2148-15042148-15042020-03-01711410.4274/jtsm.galenos.2020.2193913049054Evaluation of Sleep Structure and Sleep-related Disorders in Pediatric Patients Diagnosed with Duchenne Muscular Dystrophy and Spinal Muscular AtrophyNuran Burcu Arkalı0Gülçin Benbir Şenel1Hüseyin Kılıç2Gündüz İncesu3Sema Saltık4Cengiz Yalçınkaya5Derya Karadeniz6 İstanbul Üniversitesi-Cerrahpaşa, Cerrahpaşa Tıp Fakültesi, Nöroloji Anabilim Dalı, İstanbul, Türkiye İstanbul Üniversitesi-Cerrahpaşa, Cerrahpaşa Tıp Fakültesi, Nöroloji Anabilim Dalı, İstanbul, Türkiye İstanbul Üniversitesi-Cerrahpaşa, Cerrahpaşa Tıp Fakültesi, Çocuk Sağlığı ve Hastalıkları Anabilim Dalı, İstanbul, Türkiye İstanbul Üniversitesi-Cerrahpaşa, Cerrahpaşa Tıp Fakültesi, Nöroloji Anabilim Dalı, İstanbul, Türkiye İstanbul Üniversitesi-Cerrahpaşa, Cerrahpaşa Tıp Fakültesi, Çocuk Sağlığı ve Hastalıkları Anabilim Dalı, İstanbul, Türkiye İstanbul Üniversitesi-Cerrahpaşa, Cerrahpaşa Tıp Fakültesi, Nöroloji Anabilim Dalı, İstanbul, Türkiye İstanbul Üniversitesi-Cerrahpaşa, Cerrahpaşa Tıp Fakültesi, Nöroloji Anabilim Dalı, İstanbul, Türkiye Objective:Duchenne muscular dystrophy (DMD) is a hereditary neuromuscular disorder in which respiratory problems arise secondary to the involvement of skeletal muscles. Spinal muscular atrophy (SMA) is a disorder group characterized by the involvement of anterior horn cells. The most common respiratory problems in DMD and SMA patients are pharyngeal muscle weakness in sleep and sleep-related respiratory disorders. In this study, we evaluated sleep structure and sleep-related disorders in pediatric age group diagnosed with DMD and SMA.Materials and Methods:In pediatric patients who were diagnosed to have DMD or SMA upon genetic analysis between 2014 and 2018 were performed polysomnographic investigations in our Sleep and Disorder Units.Results:Age (p=0.074), gender (p=0.065) or Body Mass index (p=0.473) were compatible between the three groups, including 13 DMD patients, seven SMA patients, and six healthy control children. In DMD patients, although rapid eye movement (REM) sleep phase latency was longer and REM sleep phase duration was shorter compared to both healthy controls and SMA patients; it was not statistically significant. In SMA patients, total sleep time and deep non-REM (NREM) sleep duration were shorter than both healthy controls and DMD patients; though this difference was not statistically significant. Pediatric Obstructive Sleep Apnea syndrome (OSAS) was detected in three DMD patients (23.1%) and six SMA patients (85.7%), no pediatric OSAS was detected in the control group (p=0.010). Mean Apnea-hypopnea index was 2.15+4.60/ hr in DMD patients, 7.43+6.19/hr in SMA patients and 0.33+0.52/hr in control group (p=0.018).Conclusion:In our study, it was found that sleep structure is disturbed and pediatric OSAS is more commonly encountered in DMD and SMA patient groups, which two disorders causing muscle and respiratory problems due to muscular and neurogenic involvement. http://jtsm.org/archives/archive-detail/article-preview/evaluation-of-sleep-structure-and-sleep-related-di/36138 duchenne muscular dystrophyspinal muscular atrophysleepsleep-related disorderspediatric obstructive sleep apnea syndrome
collection DOAJ
language English
format Article
sources DOAJ
author Nuran Burcu Arkalı
Gülçin Benbir Şenel
Hüseyin Kılıç
Gündüz İncesu
Sema Saltık
Cengiz Yalçınkaya
Derya Karadeniz
spellingShingle Nuran Burcu Arkalı
Gülçin Benbir Şenel
Hüseyin Kılıç
Gündüz İncesu
Sema Saltık
Cengiz Yalçınkaya
Derya Karadeniz
Evaluation of Sleep Structure and Sleep-related Disorders in Pediatric Patients Diagnosed with Duchenne Muscular Dystrophy and Spinal Muscular Atrophy
Türk Uyku Tıbbı Dergisi
duchenne muscular dystrophy
spinal muscular atrophy
sleep
sleep-related disorders
pediatric obstructive sleep apnea syndrome
author_facet Nuran Burcu Arkalı
Gülçin Benbir Şenel
Hüseyin Kılıç
Gündüz İncesu
Sema Saltık
Cengiz Yalçınkaya
Derya Karadeniz
author_sort Nuran Burcu Arkalı
title Evaluation of Sleep Structure and Sleep-related Disorders in Pediatric Patients Diagnosed with Duchenne Muscular Dystrophy and Spinal Muscular Atrophy
title_short Evaluation of Sleep Structure and Sleep-related Disorders in Pediatric Patients Diagnosed with Duchenne Muscular Dystrophy and Spinal Muscular Atrophy
title_full Evaluation of Sleep Structure and Sleep-related Disorders in Pediatric Patients Diagnosed with Duchenne Muscular Dystrophy and Spinal Muscular Atrophy
title_fullStr Evaluation of Sleep Structure and Sleep-related Disorders in Pediatric Patients Diagnosed with Duchenne Muscular Dystrophy and Spinal Muscular Atrophy
title_full_unstemmed Evaluation of Sleep Structure and Sleep-related Disorders in Pediatric Patients Diagnosed with Duchenne Muscular Dystrophy and Spinal Muscular Atrophy
title_sort evaluation of sleep structure and sleep-related disorders in pediatric patients diagnosed with duchenne muscular dystrophy and spinal muscular atrophy
publisher Galenos Yayinevi
series Türk Uyku Tıbbı Dergisi
issn 2148-1504
2148-1504
publishDate 2020-03-01
description Objective:Duchenne muscular dystrophy (DMD) is a hereditary neuromuscular disorder in which respiratory problems arise secondary to the involvement of skeletal muscles. Spinal muscular atrophy (SMA) is a disorder group characterized by the involvement of anterior horn cells. The most common respiratory problems in DMD and SMA patients are pharyngeal muscle weakness in sleep and sleep-related respiratory disorders. In this study, we evaluated sleep structure and sleep-related disorders in pediatric age group diagnosed with DMD and SMA.Materials and Methods:In pediatric patients who were diagnosed to have DMD or SMA upon genetic analysis between 2014 and 2018 were performed polysomnographic investigations in our Sleep and Disorder Units.Results:Age (p=0.074), gender (p=0.065) or Body Mass index (p=0.473) were compatible between the three groups, including 13 DMD patients, seven SMA patients, and six healthy control children. In DMD patients, although rapid eye movement (REM) sleep phase latency was longer and REM sleep phase duration was shorter compared to both healthy controls and SMA patients; it was not statistically significant. In SMA patients, total sleep time and deep non-REM (NREM) sleep duration were shorter than both healthy controls and DMD patients; though this difference was not statistically significant. Pediatric Obstructive Sleep Apnea syndrome (OSAS) was detected in three DMD patients (23.1%) and six SMA patients (85.7%), no pediatric OSAS was detected in the control group (p=0.010). Mean Apnea-hypopnea index was 2.15+4.60/ hr in DMD patients, 7.43+6.19/hr in SMA patients and 0.33+0.52/hr in control group (p=0.018).Conclusion:In our study, it was found that sleep structure is disturbed and pediatric OSAS is more commonly encountered in DMD and SMA patient groups, which two disorders causing muscle and respiratory problems due to muscular and neurogenic involvement.
topic duchenne muscular dystrophy
spinal muscular atrophy
sleep
sleep-related disorders
pediatric obstructive sleep apnea syndrome
url http://jtsm.org/archives/archive-detail/article-preview/evaluation-of-sleep-structure-and-sleep-related-di/36138
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