Hickey Townsend Paige, Jones Lindsey, Tolosa Anabella, Massa Nicole, Simon Nicole A, Mylonas Dimitrios, Neumeyer Ann M, Manoach Dara S
Massachusetts General Hospital.
Res Sq. 2025 Sep 2:rs.3.rs-7419242. doi: 10.21203/rs.3.rs-7419242/v1.
Autism spectrum disorders (ASD) are a group of neurodevelopmental disorders characterized by social and communication challenges and the presence of restricted interests, repetitive behaviors, and atypical sensory processing. Sleep disturbances are prevalent in ASD and worsen daytime functioning, yet their neural bases remain poorly understood. We hypothesize that thalamocortical circuit dysfunction contributes to poor sleep in ASD. To test this hypothesis, we employ sleep EEG to determine whether sleep spindles, biomarkers of thalamocortical circuit function, are reduced in ASD and correlate with sleep quality. Since laboratory-based overnight sleep studies are costly, burdensome, and particularly problematic for individuals with ASD, we use wearable EEG headbands to record sleep in the home. This paper describes the methodology of our ongoing study of sleep in adolescents with ASD, including those with profound autism. An optional desensitization protocol helps participants gradually acclimate to the headband, promoting inclusion of individuals with sensory sensitivities and greater support needs.
We plan to enroll 80 adolescents with ASD and 80 of their typically developing peers. Participants and their families are trained remotely to use a wearable EEG headband. They also complete assessments and questionnaires. Participants who need time to acclimate follow a personalized 2-week desensitization protocol with a practice headband. Sleep is monitored at home for 3 consecutive nights, the first of which is for adaptation to sleeping with the headband. Sleep data quality is checked daily and remote technical support is provided as needed.
At-home sleep monitoring enables larger samples that are needed to characterize the neural underpinnings of sleep disturbances across the autism spectrum. The personalized desensitization protocol promotes inclusivity by accommodating individuals often excluded from research due to sensory or behavioral challenges. These methods are adaptable for other conditions and research goals beyond ASD, such as longitudinal studies across development or characterizing sleep in other neurodevelopmental disorders. Desensitization protocols may also increase the tolerability of diagnostic lab-based sleep studies and other medical procedures, improving both patient experience and quality of care.
自闭症谱系障碍(ASD)是一组神经发育障碍,其特征为社交和沟通方面存在挑战,以及存在兴趣受限、重复行为和非典型的感觉加工。睡眠障碍在ASD中很普遍,并且会使白天的功能恶化,但其神经基础仍知之甚少。我们假设丘脑皮质回路功能障碍导致了ASD患者的睡眠不佳。为了验证这一假设,我们采用睡眠脑电图来确定睡眠纺锤波(丘脑皮质回路功能的生物标志物)在ASD中是否减少,并与睡眠质量相关。由于基于实验室的夜间睡眠研究成本高昂、负担沉重,且对ASD患者尤其成问题,我们使用可穿戴脑电图头带来记录在家中的睡眠情况。本文描述了我们正在进行的针对ASD青少年(包括重度自闭症患者)睡眠研究的方法。一个可选的脱敏方案可帮助参与者逐渐适应头带,促进对有感觉敏感和更大支持需求的个体的纳入。
我们计划招募80名患有ASD的青少年及其80名发育正常的同龄人。参与者及其家人接受远程培训以使用可穿戴脑电图头带。他们还完成评估和问卷调查。需要时间适应的参与者使用练习头带遵循个性化的两周脱敏方案。在家中连续监测3个晚上的睡眠情况,第一个晚上用于适应戴着头带睡觉。每天检查睡眠数据质量,并根据需要提供远程技术支持。
在家中进行睡眠监测能够获得更大的样本,这对于描述整个自闭症谱系中睡眠障碍的神经基础是必要的。个性化的脱敏方案通过接纳那些因感觉或行为挑战而经常被排除在研究之外的个体来促进包容性。这些方法适用于ASD之外的其他情况和研究目标,例如跨发育的纵向研究或描述其他神经发育障碍中的睡眠情况。脱敏方案还可能提高基于实验室的诊断性睡眠研究和其他医疗程序的耐受性,改善患者体验和护理质量。