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Sleep Disorders in Pediatric Patients Affected by Neurofibromatosis Type 1: Reports of a Questionnaire and an Apple
Alessia Migliore1, Manuela Lo Bianco2, Roberta Leonardi1
1Pediatrics Postgraduate Residency Program, University of Catania, 95124 Catania, Italy.
Insights
Children with neurofibromatosis type 1 (NF1) experience significantly higher rates of sleep disorders, including hyperhidrosis and bruxism. Early identification and management are crucial for improving their quality of life.
Area of Science:
- Pediatric Neurology
- Sleep Medicine
- Genetics
Background:
- Sleep disturbances are common in children and can impact development and quality of life.
- Neurofibromatosis type 1 (NF1) is a genetic disorder with potential neurodevelopmental and behavioral effects.
- NF1's impact on the nervous system may increase the risk of sleep disorders in affected children.
Purpose of the Study:
- To investigate the association between NF1 and sleep disorders in pediatric patients.
- To compare the prevalence and patterns of sleep disturbances in children with NF1 versus healthy controls.
- To explore the potential neurodevelopmental links to sleep issues in NF1.
Main Methods:
- An observational case-control study involving 100 children (ages 2-12), with 50 diagnosed with NF1 and 50 healthy controls.
- Data collection via parental questionnaires on sleep disturbances (parasomnias, breathing disorders, behavioral issues).
- Objective sleep assessment using an Apple Watch Ultra for sleep quality analysis.
Main Results:
- Children with NF1 showed a significantly higher prevalence of sleep disorders compared to controls.
- Increased rates of nocturnal hyperhidrosis (48% vs. 10%), bruxism (48% vs. 28%), restless legs syndrome (22% vs. 4%), frequent nighttime awakenings (22% vs. 8%), and sleep paralysis (12% vs. 0%) in NF1 patients.
- Apple Watch Ultra analysis indicated poorer overall sleep quality in children with NF1.
Conclusions:
- Children with NF1 have an elevated risk for various sleep disorders.
- Early detection and management of sleep disturbances are vital for improving outcomes in pediatric NF1 patients.
- Further research is needed to elucidate the underlying mechanisms and develop targeted interventions.
Abstract:
Introduction: Sleep is a fundamental biological function critical for physical and mental health. Chronic sleep disturbances can significantly impair cognitive, emotional, and social functioning, leading to deficits in attention, alertness, and executive function, alongside increased irritability, anxiety, and depression. For pediatric patients, such disturbances pose additional concerns, potentially disrupting developmental processes and quality of life for both children and their families. Objectives: Emerging evidence suggests a correlation between neurofibromatosis type 1 (NF1) and an increased prevalence of sleep disorders in children. NF1, a genetic condition affecting multiple body systems, including the nervous system, may predispose children to sleep disturbances due to its neurodevelopmental and behavioral impacts. This observational case-control study aimed to explore the association between NF1 and sleep disorders in pediatric patients, comparing the prevalence and patterns of sleep disturbances between NF1 patients and healthy controls. Patients and Methods: The study included 100 children aged 2-12 years, divided into two groups: 50 with NF1 (case group) and 50 children belonging to the control group. NF1 patients were recruited from the Unit of Rare Diseases of the Nervous System in Childhood at the Policlinico "G. Rodolico-San Marco" University Hospital in Catania. Data were collected using a questionnaire completed by parents, assessing parasomnias, breathing-related sleep disorders, and other behavioral and physiological disturbances; these data were compared to a sleep assessment performed using an Apple Watch Ultra. Results: NF1 patients exhibited a significantly higher prevalence of sleep disorders than controls. Notable differences included increased nocturnal hyperhidrosis (48% vs. 10%), bruxism (48% vs. 28%), restless legs syndrome (22% vs. 4%), frequent nighttime awakenings (22% vs. 8%), and sleep paralysis (12% vs. 0%). A finding of poorer sleep quality also emerged from the results of sleep analysis using an Apple Watch Ultra. Conclusions: These findings confirm an elevated risk of sleep disorders in children with NF1, emphasizing the importance of early identification and management to improve quality of life and mitigate cognitive and behavioral impacts. Further research is essential to understand the mechanisms underlying these associations and develop targeted interventions for this population.
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