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Hypersomnia in children affected by migraine without aura: a questionnaire-based case-control study

BACKGROUND: The relationship between sleep and headache is meaningful and complex. Children affected by migraines tend to show many sleep disorders, such as insufficient sleep duration and excessive daytime somnolence. Therefore, the aim of this study is to assess the rate of reported sleep habits a...

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Autores principales: Esposito, Maria, Roccella, Michele, Parisi, Lucia, Gallai, Beatrice, Carotenuto, Marco
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3582477/
https://www.ncbi.nlm.nih.gov/pubmed/23459616
http://dx.doi.org/10.2147/NDT.S42182
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author Esposito, Maria
Roccella, Michele
Parisi, Lucia
Gallai, Beatrice
Carotenuto, Marco
author_facet Esposito, Maria
Roccella, Michele
Parisi, Lucia
Gallai, Beatrice
Carotenuto, Marco
author_sort Esposito, Maria
collection PubMed
description BACKGROUND: The relationship between sleep and headache is meaningful and complex. Children affected by migraines tend to show many sleep disorders, such as insufficient sleep duration and excessive daytime somnolence. Therefore, the aim of this study is to assess the rate of reported sleep habits and self-reported sleepiness in a large pediatric sample of individuals affected by migraine without aura (MoA). METHODS: The study population consisted of 271 children aged between 6 and 13 years affected by MoA. The control group was composed of 305 typically developing children. To assess the sleep habits of all individuals (MoA and control), parents filled out the Sleep Disturbance Scale for Children, and to check the degree of subjective perceived daytime sleepiness, all subjects were administered the Pediatric Daytime Sleepiness Scale. RESULTS: The two study groups were matched for age (P = 0.124), sex distribution (P = 0.775), and body mass index z-score (P = 0.107). Parents of children affected by MoA reported a higher total score of sleep disorder symptoms (P <0.001), disorders of initiating and maintaining (P < 0.001), and disorders of arousal (P < 0.001) than did parents of controls. No significant differences were found in disorders of excessive somnolence. Conversely, in the Pediatric Daytime Sleepiness Scale, migraine children had higher scores (24.67 ± 3.19 vs 11.94 ± 4.81; P < 0.001) and a reduction in referred total sleep time mean duration (469.83 ± 98.112 vs 527.94 ± 83.02; P < 0.001) than typically developing children. CONCLUSION: Our study identified differences in sleep habits and found a high prevalence of daytime somnolence in children affected by MoA, suggesting the need for routine sleep screening in the pediatric management of children with migraines.
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spelling pubmed-35824772013-03-04 Hypersomnia in children affected by migraine without aura: a questionnaire-based case-control study Esposito, Maria Roccella, Michele Parisi, Lucia Gallai, Beatrice Carotenuto, Marco Neuropsychiatr Dis Treat Original Research BACKGROUND: The relationship between sleep and headache is meaningful and complex. Children affected by migraines tend to show many sleep disorders, such as insufficient sleep duration and excessive daytime somnolence. Therefore, the aim of this study is to assess the rate of reported sleep habits and self-reported sleepiness in a large pediatric sample of individuals affected by migraine without aura (MoA). METHODS: The study population consisted of 271 children aged between 6 and 13 years affected by MoA. The control group was composed of 305 typically developing children. To assess the sleep habits of all individuals (MoA and control), parents filled out the Sleep Disturbance Scale for Children, and to check the degree of subjective perceived daytime sleepiness, all subjects were administered the Pediatric Daytime Sleepiness Scale. RESULTS: The two study groups were matched for age (P = 0.124), sex distribution (P = 0.775), and body mass index z-score (P = 0.107). Parents of children affected by MoA reported a higher total score of sleep disorder symptoms (P <0.001), disorders of initiating and maintaining (P < 0.001), and disorders of arousal (P < 0.001) than did parents of controls. No significant differences were found in disorders of excessive somnolence. Conversely, in the Pediatric Daytime Sleepiness Scale, migraine children had higher scores (24.67 ± 3.19 vs 11.94 ± 4.81; P < 0.001) and a reduction in referred total sleep time mean duration (469.83 ± 98.112 vs 527.94 ± 83.02; P < 0.001) than typically developing children. CONCLUSION: Our study identified differences in sleep habits and found a high prevalence of daytime somnolence in children affected by MoA, suggesting the need for routine sleep screening in the pediatric management of children with migraines. Dove Medical Press 2013 2013-02-21 /pmc/articles/PMC3582477/ /pubmed/23459616 http://dx.doi.org/10.2147/NDT.S42182 Text en © 2013 Esposito et al, publisher and licensee Dove Medical Press Ltd This is an Open Access article which permits unrestricted noncommercial use, provided the original work is properly cited.
spellingShingle Original Research
Esposito, Maria
Roccella, Michele
Parisi, Lucia
Gallai, Beatrice
Carotenuto, Marco
Hypersomnia in children affected by migraine without aura: a questionnaire-based case-control study
title Hypersomnia in children affected by migraine without aura: a questionnaire-based case-control study
title_full Hypersomnia in children affected by migraine without aura: a questionnaire-based case-control study
title_fullStr Hypersomnia in children affected by migraine without aura: a questionnaire-based case-control study
title_full_unstemmed Hypersomnia in children affected by migraine without aura: a questionnaire-based case-control study
title_short Hypersomnia in children affected by migraine without aura: a questionnaire-based case-control study
title_sort hypersomnia in children affected by migraine without aura: a questionnaire-based case-control study
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3582477/
https://www.ncbi.nlm.nih.gov/pubmed/23459616
http://dx.doi.org/10.2147/NDT.S42182
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