Evaluation of Sleep-Disordered Breathing and Respiratory Dysfunction in Children with Myotonic Dystrophy Type 1—A Retrospective Cross-Sectional Study

<b>Background/Objectives</b>: Myotonic dystrophy type 1 (DM1) is a rare neuromuscular disorder characterized by respiratory dysfunction that significantly impacts quality of life and longevity. This study aimed to explore the outcomes of pulmonary function tests and sleep-disordered breathing (SDB) workups in children with DM1 and to identify the factors contributing to SDB. <b>Methods</b>: A retrospective study examined patients' medical records, including genetic analyses, clinical characteristics, and noninvasive pulmonary function testing (PFT), when possible. The Pediatric Sleep Questionnaire (PSQ), arterial blood gases, polygraphy, and overnight transcutaneous capnometry (PtcCO<sub>2</sub>) were used to assess SDB. <b>Results</b>: The size of CTG expansion in the <i>DMPK</i> gene directly correlated with the severity of respiratory complications and the need for early tracheostomy tube insertion in 7/20 (35%) patients. A total of 13/20 (65%) children were available for respiratory evaluation during spontaneous breathing. While moderate/severe obstructive sleep apnea syndrome (OSAS) and hypoventilation were confirmed in 4/13 (31%) children, none of the patients had mixed or dominantly central sleep apnea syndrome. There was no correlation between apnea-hypopnea index (AHI) or PtcCO<sub>2</sub> and the presence of SDB-related symptoms or the PSQ score. Although a significant correlation between AHI and PtcCO<sub>2</sub> was not confirmed (<i>p</i> = 0.447), the oxygen desaturation index directly correlated with PtcCO<sub>2</sub> (<i>p</i> = 0.014). <b>Conclusions</b>: While SDB symptoms in children with DM1 may not fully correlate with observed respiratory events or impaired gas exchange during sleep, a comprehensive screening for SDB should be considered for all patients with DM1. Further research into disease-specific recommendations encompassing the standardization of PFT, as well as overnight polygraphic and capnometry recordings, could help to guide timely, personalized treatment.

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Journal
Biomedicines
Published
2025-04-15
DOI
https://doi.org/10.3390/biomedicines13040966
Citations
1
Primary Topic
Genetic Neurodegenerative Diseases
Type
article
Field-Weighted Citation Impact
0.91
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article

Evaluation of Sleep-Disordered Breathing and Respiratory Dysfunction in Children with Myotonic Dystrophy Type 1—A Retrospective Cross-Sectional Study

Alessandro Amaddeo, Dušanka Savić‐Pavićević, Jovan Pešović, Aleksandar Sovtić et al.
1 citations
Biomedicines
Genetic Neurodegenerative Diseases
0.91
article

Evaluation of Sleep-Disordered Breathing and Respiratory Dysfunction in Children with Myotonic Dystrophy Type 1—A Retrospective Cross-Sectional Study

Alessandro Amaddeo, Dušanka Savić‐Pavićević, Jovan Pešović, Aleksandar Sovtić, Slavica Ostojić, Mihail Baša, Stojan Perić, Giovanni Meola, Gordana Kovačević
article en
1 citations

Abstract

<b>Background/Objectives</b>: Myotonic dystrophy type 1 (DM1) is a rare neuromuscular disorder characterized by respiratory dysfunction that significantly impacts quality of life and longevity. This study aimed to explore the outcomes of pulmonary function tests and sleep-disordered breathing (SDB) workups in children with DM1 and to identify the factors contributing to SDB. <b>Methods</b>: A retrospective study examined patients' medical records, including genetic analyses, clinical characteristics, and noninvasive pulmonary function testing (PFT), when possible. The Pediatric Sleep Questionnaire (PSQ), arterial blood gases, polygraphy, and overnight transcutaneous capnometry (PtcCO<sub>2</sub>) were used to assess SDB. <b>Results</b>: The size of CTG expansion in the <i>DMPK</i> gene directly correlated with the severity of respiratory complications and the need for early tracheostomy tube insertion in 7/20 (35%) patients. A total of 13/20 (65%) children were available for respiratory evaluation during spontaneous breathing. While moderate/severe obstructive sleep apnea syndrome (OSAS) and hypoventilation were confirmed in 4/13 (31%) children, none of the patients had mixed or dominantly central sleep apnea syndrome. There was no correlation between apnea-hypopnea index (AHI) or PtcCO<sub>2</sub> and the presence of SDB-related symptoms or the PSQ score. Although a significant correlation between AHI and PtcCO<sub>2</sub> was not confirmed (<i>p</i> = 0.447), the oxygen desaturation index directly correlated with PtcCO<sub>2</sub> (<i>p</i> = 0.014). <b>Conclusions</b>: While SDB symptoms in children with DM1 may not fully correlate with observed respiratory events or impaired gas exchange during sleep, a comprehensive screening for SDB should be considered for all patients with DM1. Further research into disease-specific recommendations encompassing the standardization of PFT, as well as overnight polygraphic and capnometry recordings, could help to guide timely, personalized treatment.

BiomedicinesVol. 13(4)
University of Milan (IT), IRCCS Materno Infantile Burlo Garofolo (IT), University of Belgrade (RS), Centar za Promociju Nauke (RS), Casa di Cura Columbus (IT), Institute of Public Health of Serbia (RS)
Good health and well-being
Openalex Percentile: Top 28%
Genetic Neurodegenerative Diseases
0.91
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