对患有自闭症的幼儿和日后更有可能被诊断为自闭症的儿童进行头戴式眼动追踪研究

IF 4.1 2区 医学 Q1 CLINICAL NEUROLOGY Journal of Neurodevelopmental Disorders Pub Date : 2024-03-04 DOI:10.1186/s11689-024-09524-1
E. Perkovich, A. Laakman, S. Mire, H. Yoshida
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引用次数: 0

摘要

在过去几年中,研究人员一直在使用头戴式眼动跟踪系统研究幼儿在日常活动中的注视行为,通过这些活动,幼儿可以了解世界。这种方法具有巨大的潜力,能让我们进一步了解毫秒级别的注视行为是如何创造多感官体验并在社会环境中波动的。虽然这项工作能让我们深入了解早期感知经验和潜在的学习机制,但大部分工作都是针对发育正常的儿童开展的。在发育障碍儿童中,感官敏感性、社会交流障碍和挑战性行为(如干扰、离家出走)很常见,这可能是收集高质量数据的潜在方法论挑战。在本文中,我们介绍了使用头戴式眼动仪对 41 名自闭症儿童和 17 名日后被诊断为自闭症可能性增加但无听力或视力障碍的儿童(包括那些很少说话或不说话和/或有智力障碍的儿童)进行跟踪的研究实践。自闭症儿童的数据收集成功率为 92.68%。41 名儿童中有 3 名未能完成游戏环节,因此 1-4 岁儿童的成功率为 86.36%,5-8 岁儿童的成功率为 100.00%。在 17 名日后更有可能被诊断为自闭症的儿童中,有 1 名未能完成游戏环节,因此成功率为 94.11%。与该方法相关的 "挑战性 "行为很多。最常见的挑战性行为包括摘下眼动仪、逃跑和苦恼。总体而言,在自闭症儿童中,88.8% 的 1-4 岁儿童和 29.4% 的 5-8 岁儿童至少表现出一种挑战行为。利用这种方法进行的研究有可能揭示出与自闭症筛查、诊断和干预相关的早期社会中介凝视行为。我们希望,我们在记录研究方法方面所做的努力能帮助研究人员和临床医生利用头戴式眼动仪有效地研究儿童在非实验情境下的早期自然发生的注视行为,包括自闭症和其他发育障碍。最终,这种应用可能会提高研究结果的普遍性,更好地反映个体特征的多样性,并为这一方法在该领域的应用提供新的途径。
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Conducting head-mounted eye-tracking research with young children with autism and children with increased likelihood of later autism diagnosis
Over the past years, researchers have been using head-mounted eye-tracking systems to study young children’s gaze behaviors in everyday activities through which children learn about the world. This method has great potential to further our understanding of how millisecond-level gaze behaviors create multisensory experiences and fluctuate around social environments. While this line of work can yield insight into early perceptual experiences and potential learning mechanisms, the majority of the work is exclusively conducted with typically-developing children. Sensory sensitivities, social-communication difficulties, and challenging behaviors (e.g., disruption, elopement) are common among children with developmental disorders, and they may represent potential methodological challenges for collecting high-quality data. In this paper, we describe our research practices of using head-mounted eye trackers with 41 autistic children and 17 children with increased likelihood of later autism diagnosis without auditory or visual impairments, including those who are minimally or nonspeaking and/or have intellectual disabilities. The success rate in gathering data among children with autism was 92.68%. 3 of 41 children failed to complete the play-session, resulting in an 86.36% success rate among 1–4-year-olds and a 100.00% success rate among 5–8-year-olds. 1 of 17 children with increased likelihood of later autism diagnosis failed to complete the play-session, resulting in a success rate of 94.11%. There were numerous “challenging” behaviors relevant to the method. The most common challenging behaviors included taking the eye-tracking device off, elopement, and becoming distressed. Overall, among children with autism, 88.8% of 1–4-year-olds and 29.4% of 5–8-year-olds exhibited at least one challenging behavior. Research capitalizing on this methodology has the potential to reveal early, socially-mediated gaze behaviors that are relevant for autism screening, diagnosis, and intervention purposes. We hope that our efforts in documenting our study methodology will help researchers and clinicians effectively study early naturally-occuring gaze behaviors of children during non-experimental contexts across the spectrum and other developmental disabilities using head-mounted eye-tracking. Ultimately, such applications may increase the generalizability of results, better reflect the diversity of individual characteristics, and offer new ways in which this method can contribute to the field.
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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.
期刊最新文献
Investigating social orienting in children with Phelan-McDermid syndrome and 'idiopathic' autism. Predicting neurodevelopmental disorders using machine learning models and electronic health records - status of the field. The utility of wearable electroencephalography combined with behavioral measures to establish a practical multi-domain model for facilitating the diagnosis of young children with attention-deficit/hyperactivity disorder. Early onset and increasing disparities in neurodevelopmental delays from birth to age 6 in children from low socioeconomic backgrounds. The effect of anxiety and autism symptom severity on restricted and repetitive behaviors over time in children with fragile X syndrome.
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