Winston Molly, Nayar Kritika, Landau Emily, Maltman Nell, Sideris John, Zhou Lili, Sharp Kevin, Berry-Kravis Elizabeth, Losh Molly
Roxelyn and Richard Pepper Department of Communication Sciences and Disorders, Northwestern University, Evanston, IL, United States.
Chan Division of Occupational Science and Occupational Therapy, University of Southern California, Los Angeles, CA, United States.
Front Genet. 2021 Feb 9;12:591211. doi: 10.3389/fgene.2021.591211. eCollection 2021.
Atypical visual attention patterns have been observed among carriers of the fragile X mental retardation gene () premutation (PM), with some similarities to visual attention patterns observed in autism spectrum disorder (ASD) and among clinically unaffected relatives of individuals with ASD. Patterns of visual attention could constitute biomarkers that can help to inform the neurocognitive profile of the PM, and that potentially span diagnostic boundaries. This study examined patterns of eye movement across an array of fixation measurements from three distinct eye-tracking tasks in order to investigate potentially overlapping profiles of visual attention among PM carriers, ASD parents, and parent controls. Logistic regression analyses were conducted to examine whether variables constituting a PM-specific looking profile were able to effectively predict group membership. Participants included 65PM female carriers, 188 ASD parents, and 84 parent controls. Analyses of fixations across the eye-tracking tasks, and their corresponding areas of interest, revealed a distinct visual attention pattern in carriers of the PM, characterized by increased fixations on the mouth when viewing faces, more intense focus on bodies in socially complex scenes, and decreased fixations on salient characters and faces while narrating a wordless picture book. This set of variables was able to successfully differentiate individuals with the PM from controls (Sensitivity = 0.76, Specificity = 0.85, Accuracy = 0.77) as well as from ASD parents (Sensitivity = 0.70, Specificity = 0.80, Accuracy = 0.72), but did not show a strong distinction between ASD parents and controls (Accuracy = 0.62), indicating that this set of variables comprises a profile that is unique to PM carriers. Regarding predictive power, fixations toward the mouth when viewing faces was able to differentiate PM carriers from both ASD parents and controls, whereas fixations toward other social stimuli did not differentiate PM carriers from ASD parents, highlighting some overlap in visual attention patterns that could point toward shared neurobiological mechanisms. Results demonstrate a profile of visual attention that appears strongly associated with the PM in women, and may constitute a meaningful biomarker.
在脆性X智力障碍基因()前突变(PM)携带者中观察到了非典型的视觉注意力模式,这与自闭症谱系障碍(ASD)以及ASD患者临床未受影响亲属中观察到的视觉注意力模式有一些相似之处。视觉注意力模式可能构成生物标志物,有助于了解PM的神经认知概况,并可能跨越诊断界限。本研究通过三个不同眼动追踪任务中的一系列注视测量来检查眼动模式,以调查PM携带者、ASD父母和父母对照组之间潜在重叠的视觉注意力概况。进行逻辑回归分析,以检查构成PM特异性注视概况的变量是否能够有效预测组别归属。参与者包括65名PM女性携带者、188名ASD父母和84名父母对照组。对眼动追踪任务中的注视及其相应感兴趣区域的分析显示,PM携带者存在独特的视觉注意力模式,其特征为在观看面部时对嘴巴的注视增加、在社会复杂场景中对身体的关注更强烈,以及在讲述无字图画书时对突出角色和面部的注视减少。这组变量能够成功区分PM个体与对照组(敏感性=0.76,特异性=0.85,准确性=0.77)以及与ASD父母(敏感性=0.70,特异性=0.80,准确性=0.72),但在ASD父母和对照组之间没有显示出强烈差异(准确性=0.62),表明这组变量构成了PM携带者特有的概况。关于预测能力,观看面部时对嘴巴的注视能够区分PM携带者与ASD父母和对照组,而对其他社会刺激的注视则无法区分PM携带者与ASD父母,这突出了视觉注意力模式中的一些重叠,可能指向共同的神经生物学机制。结果表明,一种视觉注意力概况似乎与女性中的PM密切相关,可能构成一种有意义的生物标志物。