Synchronisation of circadian timing in families and the impact of autism: a scoping review.

IF 3.6 2区 医学 Q1 CLINICAL NEUROLOGY
Aoife Brennan, Cathy Wyse, Mailton Vasconcelos, Laura Rudderham, Louise Gallagher, Lorna M Lopez
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引用次数: 0

Abstract

Autism Spectrum Disorder (autism) is a neurodevelopmental condition characterised by altered social communication, repetitive behaviours and restricted interests. Emerging evidence suggests that disrupted circadian timing mechanisms may be associated with certain traits of autism, such as sleep difficulties and behavioural dysregulation. Circadian rhythms are primarily entrained by the light–dark cycle but are also shaped by social cues, including synchronisation with the circadian rhythms of family members. Despite growing interest in circadian biology and autism, little is known about how circadian synchrony functions within families that include autistic children. This scoping review synthesises findings on circadian timing in families with autistic and non-autistic children. A systematic search of four databases (PubMed, Scopus, PsycINFO, and CINAHL) yielded 2,423 results, of which 25 met inclusion criteria. An additional 17 studies were identified through handsearching. The final dataset comprised 42 studies, which were organised into a narrative synthesis and thematic analysis. Six studies focused on sleep synchrony in families with autistic children, while the remaining 36 studies examined circadian biomarkers (n = 5), activity rhythms (n = 12), and sleep synchrony (n = 19) in families with non-autistic children. Findings revealed evidence of circadian synchrony in both groups, with family members displaying aligned sleep–wake patterns and daily activity rhythms. However, studies involving autistic families were relatively limited, and the mechanisms underlying circadian synchrony remain poorly understood. While this review highlights emerging insights into circadian synchrony in families, significant gaps in the literature remain. Research in autistic families is particularly scarce, and there is a need for longitudinal and experimental studies to better understand the interplay between genetic, environmental and social factors. Further research should explore whether disrupted circadian synchrony contributes to the neurobiology of autism or its associated traits, such as sleep difficulties and behavioural dysregulation. Addressing these gaps could inform targeted interventions to improve sleep and overall well-being in autistic children and their families.

家庭中昼夜节律时间的同步和自闭症的影响:范围审查。
自闭症谱系障碍(Autism Spectrum Disorder, Autism)是一种神经发育疾病,其特征是社会沟通改变、行为重复和兴趣受限。新出现的证据表明,生物钟紊乱可能与自闭症的某些特征有关,比如睡眠困难和行为失调。昼夜节律主要受昼夜周期的影响,但也受社会因素的影响,包括与家庭成员的昼夜节律同步。尽管人们对昼夜节律生物学和自闭症的兴趣日益浓厚,但对于包括自闭症儿童在内的家庭中昼夜节律同步是如何起作用的,人们知之甚少。本综述综合了自闭症和非自闭症儿童家庭的昼夜节律时间。对四个数据库(PubMed, Scopus, PsycINFO和CINAHL)进行系统搜索,得到2423个结果,其中25个符合纳入标准。通过手工检索确定了另外17项研究。最终的数据集包括42项研究,这些研究被组织成叙事综合和主题分析。6项研究关注自闭症儿童家庭的睡眠同步性,而其余36项研究则研究了非自闭症儿童家庭的昼夜生物标志物(n = 5)、活动节律(n = 12)和睡眠同步性(n = 19)。研究结果揭示了两组人的昼夜节律同步的证据,家庭成员表现出一致的睡眠-觉醒模式和日常活动节奏。然而,涉及自闭症家庭的研究相对有限,昼夜节律同步的机制仍然知之甚少。虽然这篇综述强调了对家庭昼夜节律同步的新见解,但文献中仍然存在重大空白。对自闭症家庭的研究尤其缺乏,需要进行纵向和实验研究,以更好地了解遗传、环境和社会因素之间的相互作用。进一步的研究应该探索昼夜节律同步中断是否有助于自闭症的神经生物学或其相关特征,如睡眠困难和行为失调。解决这些差距可以为有针对性的干预提供信息,以改善自闭症儿童及其家庭的睡眠和整体健康。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
7.60
自引率
4.10%
发文量
58
审稿时长
>12 weeks
期刊介绍: Journal of Neurodevelopmental Disorders is an open access journal that integrates current, cutting-edge research across a number of disciplines, including neurobiology, genetics, cognitive neuroscience, psychiatry and psychology. The journal’s primary focus is on the pathogenesis of neurodevelopmental disorders including autism, fragile X syndrome, tuberous sclerosis, Turner Syndrome, 22q Deletion Syndrome, Prader-Willi and Angelman Syndrome, Williams syndrome, lysosomal storage diseases, dyslexia, specific language impairment and fetal alcohol syndrome. With the discovery of specific genes underlying neurodevelopmental syndromes, the emergence of powerful tools for studying neural circuitry, and the development of new approaches for exploring molecular mechanisms, interdisciplinary research on the pathogenesis of neurodevelopmental disorders is now increasingly common. Journal of Neurodevelopmental Disorders provides a unique venue for researchers interested in comparing and contrasting mechanisms and characteristics related to the pathogenesis of the full range of neurodevelopmental disorders, sharpening our understanding of the etiology and relevant phenotypes of each condition.
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