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Published on: October 2, 2019
Sleep in Children With Pallister Killian Syndrome: A Prospective Clinical and Videopolysomnographic Study
Anna Fetta1,2, Veronica Di Pisa1, Martina Ruscelli2
1IRCCS Istituto delle Scienze Neurologiche di Bologna, UOC di Neuropsichiatria dell'Età Pediatrica, Bologna, Italy.
Insights
This study reveals significant sleep disturbances in children with Pallister-Killian syndrome (PKS), including issues with initiating and maintaining sleep and sleep breathing disorders. Early screening using the Sleep Disturbance Scale for Children (SDSC) is recommended for effective intervention.
Area of Science:
- Genetics
- Sleep Medicine
- Pediatrics
Background:
- Pallister-Killian syndrome (PKS) is a rare genetic disorder characterized by mosaic tetrasomy of chromosome 12p, often associated with multi-organ involvement.
- Caregivers frequently report sleep impairments in children with PKS, yet systematic data are lacking.
Purpose of the Study:
- To characterize sleep features in Pallister-Killian syndrome.
- To identify clinical and demographic factors influencing sleep patterns.
- To evaluate the effectiveness of standard screening questionnaires for sleep disorders in PKS patients.
Main Methods:
- Prospective enrollment of 14 PKS patients (aged 1-17 years).
- Administration of the Sleep Disturbance Scale for Children (SDSC) questionnaire to caregivers.
- Performance of 24-hour video polysomnography (VPSG) and comparison with a control group.
Main Results:
- 92% of PKS patients exhibited abnormal SDSC scores, particularly in 'disorder of initiating and maintaining sleep' and 'sleep breathing disorders' subscales.
- VPSG revealed impaired sleep macrostructure in PKS patients, including higher Arousal Index, increased time in N3 sleep, and reduced Sleep Efficiency.
- PKS children showed a significantly increased Apnea-Hypopnea Index (AHI) compared to controls, correlating with SDSC 'sleep breathing disorders' scores.
Conclusions:
- This study provides the first description of sleep patterns in PKS, confirming a high prevalence of sleep disorders.
- Investigating and treating sleep disorders is crucial for PKS patients.
- The SDSC is an effective screening tool for early detection of sleep disorders, especially breathing issues, in this population.
Abstract:
Objectives: Pallister-Killian syndrome (PKS) is a rare genetic disorder with multi-organ involvement caused by mosaic tetrasomy of chromosome 12p. Although many caregivers report the presence of impaired sleep in their children, there are no clear data in the literature on this issue and no systematic study has ever been performed. With this study, we aimed to characterize the features of sleep in Pallister-Killian syndrome and identify the possible influence of clinical and demographic features. Moreover, our aim was to verify the effectiveness of conventional screening questionnaires in this particular group of patients. Methods: We prospectively enrolled 14 patients aged 1-17 years in collaboration with PKS Kids Italia ONLUS. The Sleep Disturbance Scale for Children (SDSC) questionnaire was administered to caregivers. Then, video polysomnography (VPSG) of at least 24 h was performed and results were compared with a same-aged control group. Results: A total of 92% of patients had abnormal SDSC scores, extremely high in the "disorder of initiating and maintaining sleep" (DIMS) and "sleep breathing disorders" (SBD) subscales. VPSG showed a significantly impaired macrostructure in PKS patients, with a higher Arousal Index (p < 0.00001) and percentage of time spent in N3 (p < 0.00001), and reduced Sleep Efficiency (p = 0.0006). After dividing both PKS and controls into two groups based on median age, some peculiarities emerged: the younger group had higher Awakenings Index (p = 0.0207) and percentage of time spent in N1 (p = 0.015) while the older group showed higher time in bed (TIB) (p = 0.0485), compared with controls. Due to poor compliance, the Apnea-Hypopnea Index (AHI) was evaluated only for 10 PKS children, being significantly increased (p = 0.0427) compared with controls. SBD subscale scores in SDSC were significantly related to AHI values in VPSG (p = 0.0099). Conclusions: This study constitutes the first attempt to describe the sleep pattern in PKS. Despite small numbers due to the rarity of the syndrome, our VPSG results confirm the high prevalence of sleep disorders (SDs) in these patients. It is therefore essential to investigate and treat them. The SDSC scale is a good screening tool for early detection also in these patients, with particular sensitivity in detecting breathing disorders.
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