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    Study protocol: assessing SleeP IN infants with early-onset atopic Dermatitis by Longitudinal Evaluation (The SPINDLE study).

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    Authors
    O'Connor, Cathal cc
    Irvine, Alan cc
    Murray, Deirdre cc
    Murphy , Michelle cc
    Hourihane, Jonathan cc
    Boylan, Geraldine cc
    Issue Date
    2022-06-18
    Keywords
    Actigraphy
    atopic dermatitis
    early intervention
    Electroencepalography
    Parental sleep disruption
    sleep
    Sleep diaries
    Sleep disruption
    
    Metadata
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    Journal
    BMC pediatrics
    URI
    http://hdl.handle.net/10147/634905
    DOI
    10.1186/s12887-022-03382-3
    PubMed ID
    35717147
    PubMed Central ID
    PMC9206384
    Abstract
    Background: Atopic dermatitis (AD) is the most common chronic inflammatory skin condition in childhood. Most (50-60%) children with AD report sleep disturbance, which is secondary to itch, dry skin, inflammation, and abnormal circadian rhythm. Sleep is essential for brain development, learning, and growth. Sleep disruption in early life is associated with cognitive and psychological dysfunction in later life. The aim of this study is to describe in detail the sleep architecture of infants with early-onset atopic dermatitis (AD), compared to controls, by using EEG polysomnography, sleep actigraphy, and parental reporting. Methods: This observational study will recruit six- to eight-month old infants with moderate to severe AD and age-matched control infants who do not have AD. At six-eight months diurnal sleep electroencephalography and polysomnography will be performed in our research center. Nocturnal sleep actigraphy will be performed at home for five consecutive nights at six-eight months and 12 months. Between six and 12 months, monthly questionnaires will capture data on quantitative sleep and parental sleep. Skin barrier and immune profiles will be captured at six-eight and 12 months. AD will be assessed using standardized severity assessment tools and treated according to protocol. A neurodevelopmental assessment will be performed at 18 months to assess cognition and behaviour. An estimated sample size of 50 participants in each group is required to power the primary outcome of disturbed macrostructure of sleep and secondary outcomes of disturbed microstructure of sleep, and disturbed parental sleep, assuming an attrition rate of 60%. Potential confounding factors which will be controlled for in the data analysis will include parental educational level, parental depression, feeding practice, and number of siblings. Discussion: This study will provide a rich analysis of sleep in infants with AD in the first year of life using detailed electroencephalography, novel actigraphy techniques, and longitudinal parent-reported data. It may provide guidance on the optimal treatment of AD to prevent or reduce sleep disruption. Trial registration: clinicaltrials.gov NCT05031754 , retrospectively registered on September 2nd, 2021.
    Item Type
    Article
    Language
    en
    EISSN
    1471-2431
    ae974a485f413a2113503eed53cd6c53
    10.1186/s12887-022-03382-3
    Scopus Count
    Collections
    Cork University Hospital

    entitlement

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