Altered sleep architecture in children and adolescents with Down syndrome.

IF 2.8 3区 医学 Q2 GENETICS & HEREDITY American Journal of Medical Genetics Part C: Seminars in Medical Genetics Pub Date : 2023-12-01 Epub Date: 2023-10-23 DOI:10.1002/ajmg.c.32073
Kelly J Gardner, Wei Wang, Elizabeth B Klerman
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Abstract

Objective: Children with Down syndrome (DS) may experience changes in sleep architecture (i.e., different sleep stages) that then affect waketime functioning, including learning, mood, and disruptive behavior. For designing and testing interventions, it is important to document any differences in sleep architecture in children with DS with and without co-occurring diagnoses, including neuropsychiatric diagnoses and obstructive sleep apnea (OSA).

Methods: A retrospective cohort study was performed at Massachusetts General Hospital for children and adolescents with DS who underwent polysomnography (PSG) between August 2016 and July 2022. Patient data collected from the electronic medical record included diagnoses, age at PSG, and PSG report. Statistical analysis included unpaired T tests to test hypotheses about differences in sleep architecture within age groups, and differences between children with DS and a co-occurring diagnosis. One way ANOVA was used to determine statistical significance of OSA severity within patients with DS.

Results: When compared by age group, those with DS had negative changes in sleep architecture (e.g., less sleep and more wake) when compared to normative data. Within this cohort, having a co-occurring diagnosis of autism resulted in further, negative effects on sleep architecture. 89% of those with DS had diagnosed OSA but only those with severe OSA experienced negative effects on sleep architecture.

Conclusion: Age is an important covariate when studying the sleep of children with DS and neurotypical children. Studies are needed to test whether minimizing the observed differences in sleep architecture will translate to improved learning, mood, and behavioral outcomes, and how treating OSA affects sleep architecture.

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唐氏综合症儿童和青少年睡眠结构的改变。
目的:唐氏综合症(DS)儿童可能会经历睡眠结构的变化(即不同的睡眠阶段),从而影响觉醒功能,包括学习、情绪和破坏性行为。对于设计和测试干预措施,重要的是要记录患有和不患有合并诊断的DS儿童睡眠结构的任何差异,包括神经精神诊断和阻塞性睡眠呼吸暂停(OSA)。方法:在马萨诸塞州总医院对2016年8月至2022年7月期间接受多导睡眠图(PSG)检查的DS儿童和青少年进行回顾性队列研究。从电子病历中收集的患者数据包括诊断、PSG年龄和PSG报告。统计分析包括非配对T检验,以检验关于年龄组内睡眠结构差异的假设,以及DS儿童与合并诊断之间的差异。单因素方差分析用于确定DS患者OSA严重程度的统计学意义。结果:与标准数据相比,按年龄组进行比较时,DS患者的睡眠结构发生了负面变化(例如,睡眠较少,醒来次数较多)。在这一队列中,同时被诊断为自闭症会对睡眠结构产生进一步的负面影响。89%的DS患者被诊断为OSA,但只有那些患有严重OSA的患者对睡眠结构产生了负面影响。结论:年龄是研究DS儿童和神经正常儿童睡眠的重要协变量。需要进行研究,以测试将观察到的睡眠结构差异降至最低是否会转化为学习、情绪和行为结果的改善,以及OSA的治疗如何影响睡眠结构。
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来源期刊
CiteScore
7.00
自引率
0.00%
发文量
42
审稿时长
>12 weeks
期刊介绍: Seminars in Medical Genetics, Part C of the American Journal of Medical Genetics (AJMG) , serves as both an educational resource and review forum, providing critical, in-depth retrospectives for students, practitioners, and associated professionals working in fields of human and medical genetics. Each issue is guest edited by a researcher in a featured area of genetics, offering a collection of thematic reviews from specialists around the world. Seminars in Medical Genetics publishes four times per year.
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