The use of eye-tracking technology as a tool to evaluate social cognition in people with an intellectual disability: a systematic review and meta-analysis.

IF 4.1 2区 医学 Q1 CLINICAL NEUROLOGY Journal of Neurodevelopmental Disorders Pub Date : 2023-12-04 DOI:10.1186/s11689-023-09506-9
L A Jenner, E K Farran, A Welham, C Jones, J Moss
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Abstract

Background: Relatively little is known about social cognition in people with intellectual disability (ID), and how this may support understanding of co-occurring autism. A limitation of previous research is that traditional social-cognitive tasks place a demand on domain-general cognition and language abilities. These tasks are not suitable for people with ID and lack the sensitivity to detect subtle social-cognitive processes. In autism research, eye-tracking technology has offered an effective method of evaluating social cognition-indicating associations between visual social attention and autism characteristics. The present systematic review synthesised research which has used eye-tracking technology to study social cognition in ID. A meta-analysis was used to explore whether visual attention on socially salient regions (SSRs) of stimuli during these tasks correlated with degree of autism characteristics presented on clinical assessment tools.

Method: Searches were conducted using four databases, research mailing lists, and citation tracking. Following in-depth screening and exclusion of studies with low methodological quality, 49 articles were included in the review. A correlational meta-analysis was run on Pearson's r values obtained from twelve studies, reporting the relationship between visual attention on SSRs and autism characteristics.

Results and conclusions: Eye-tracking technology was used to measure different social-cognitive abilities across a range of syndromic and non-syndromic ID groups. Restricted scan paths and eye-region avoidance appeared to impact people's ability to make explicit inferences about mental states and social cues. Readiness to attend to social stimuli also varied depending on social content and degree of familiarity. A meta-analysis using a random effects model revealed a significant negative correlation (r = -.28, [95% CI -.47, -.08]) between visual attention on SSRs and autism characteristics across ID groups. Together, these findings highlight how eye-tracking can be used as an accessible tool to measure more subtle social-cognitive processes, which appear to reflect variability in observable behaviour. Further research is needed to be able to explore additional covariates (e.g. ID severity, ADHD, anxiety) which may be related to visual attention on SSRs, to different degrees within syndromic and non-syndromic ID groups, in order to determine the specificity of the association with autism characteristics.

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运用眼动追踪技术评估智障人士的社会认知:系统回顾与元分析。
背景:相对而言,人们对智力残疾(ID)患者的社会认知知之甚少,以及这如何支持对并发自闭症的理解。传统的社会认知任务对领域认知和语言能力提出了要求,这是以往研究的一个局限性。这些任务不适合ID患者,他们缺乏察觉微妙社会认知过程的敏感度。在自闭症研究中,眼动追踪技术为评估视觉社会注意与自闭症特征之间的社会认知指示关系提供了一种有效的方法。本系统综述了利用眼动追踪技术研究身份识别社会认知的研究成果。本研究采用荟萃分析的方法探讨这些任务中刺激的社会突出区域的视觉注意是否与临床评估工具中呈现的自闭症特征程度相关。方法:使用四个数据库、研究邮件列表和引文跟踪进行检索。在深入筛选和排除方法学质量较低的研究后,49篇文章被纳入本综述。对从12项研究中获得的Pearson’s r值进行相关荟萃分析,报告了ssr的视觉注意与自闭症特征之间的关系。结果和结论:眼动追踪技术被用于测量不同的社会认知能力在一系列综合征和非综合征ID组。受限的扫描路径和眼睛区域回避似乎会影响人们对精神状态和社会线索做出明确推断的能力。对社会刺激的准备程度也因社会内容和熟悉程度而异。使用随机效应模型的荟萃分析显示显著负相关(r = -)。28, [95% ci -。][47, - 0.08])。总之,这些发现强调了眼动追踪可以作为一种易于使用的工具来测量更微妙的社会认知过程,这些过程似乎反映了可观察行为的可变性。为了确定与自闭症特征相关的特异性,需要进一步的研究来探索其他可能在不同程度上与ssr视觉注意相关的共变量(如ID严重程度、ADHD、焦虑),在综合征和非综合征ID组中。
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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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