Development of webcam-collected and artificial-intelligence-derived social and cognitive performance measures for neurodevelopmental genetic syndromes

IF 2.8 3区 医学 Q2 GENETICS & HEREDITY American Journal of Medical Genetics Part C: Seminars in Medical Genetics Pub Date : 2023-08-03 DOI:10.1002/ajmg.c.32058
Thomas W. Frazier, Robyn M. Busch, Patricia Klaas, Katherine Lachlan, Shafali Jeste, Alexander Kolevzon, Eva Loth, Jacqueline Harris, Leslie Speer, Tom Pepper, Kristin Anthony, J. Michael Graglia, Christal G. Delagrammatikas, Sandra Bedrosian-Sermone, Constance Smith-Hicks, Katie Huba, Robert Longyear, LeeAnne Green-Snyder, Frederick Shic, Mustafa Sahin, Charis Eng, Antonio Y. Hardan, Mirko Uljarević
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引用次数: 1

Abstract

This study focused on the development and initial psychometric evaluation of a set of online, webcam-collected, and artificial intelligence-derived patient performance measures for neurodevelopmental genetic syndromes (NDGS). Initial testing and qualitative input was used to develop four stimulus paradigms capturing social and cognitive processes, including social attention, receptive vocabulary, processing speed, and single-word reading. The paradigms were administered to a sample of 375 participants, including 163 with NDGS, 56 with idiopathic neurodevelopmental disability (NDD), and 156 neurotypical controls. Twelve measures were created from the four stimulus paradigms. Valid completion rates varied from 87 to 100% across measures, with lower but adequate completion rates in participants with intellectual disability. Adequate to excellent internal consistency reliability (α = 0.67 to 0.95) was observed across measures. Test–retest reproducibility at 1-month follow-up and stability at 4-month follow-up was fair to good (r = 0.40–0.73) for 8 of the 12 measures. All gaze-based measures showed evidence of convergent and discriminant validity with parent-report measures of other cognitive and behavioral constructs. Comparisons across NDGS groups revealed distinct patterns of social and cognitive functioning, including people with PTEN mutations showing a less impaired overall pattern and people with SYNGAP1 mutations showing more attentional, processing speed, and social processing difficulties relative to people with NFIX mutations. Webcam-collected performance measures appear to be a reliable and potentially useful method for objective characterization and monitoring of social and cognitive processes in NDGS and idiopathic NDD. Additional validation work, including more detailed convergent and discriminant validity analyses and examination of sensitivity to change, is needed to replicate and extend these observations.

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开发网络摄像头收集和人工智能衍生的神经发育遗传综合征的社会和认知表现测量。
这项研究的重点是开发一套在线、网络摄像头收集和人工智能衍生的神经发育遗传综合征(NDGS)患者表现测量方法,并对其进行初步心理测量评估。最初的测试和定性输入用于开发四种捕捉社会和认知过程的刺激范式,包括社会注意力、接受性词汇、处理速度和单词阅读。对375名参与者进行了研究,其中163名患有NDGS,56名患有特发性神经发育障碍(NDD),156名神经正常对照。根据四种刺激模式制定了十二项措施。有效完成率从87%到100%不等,智障参与者的完成率较低但足够。足以实现卓越的内部一致性可靠性(α = 0.67至0.95)。1个月随访时的重复性和4个月随访的稳定性为一般至良好(r = 0.40-0.73)。所有基于凝视的测量都显示出与其他认知和行为结构的父母报告测量的收敛和判别有效性的证据。NDGS组之间的比较揭示了不同的社会和认知功能模式,包括PTEN突变的人总体模式受损程度较低,SYNGAP1突变的人与NFIX突变的人相比,注意力、处理速度和社会处理困难更大。网络摄像头收集的表现测量似乎是一种可靠且潜在有用的方法,用于客观表征和监测NDGS和特发性NDD的社会和认知过程。需要进行额外的验证工作,包括更详细的收敛和判别有效性分析以及对变化敏感性的检查,以复制和扩展这些观察结果。
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来源期刊
CiteScore
7.00
自引率
0.00%
发文量
42
审稿时长
>12 weeks
期刊介绍: Seminars in Medical Genetics, Part C of the American Journal of Medical Genetics (AJMG) , serves as both an educational resource and review forum, providing critical, in-depth retrospectives for students, practitioners, and associated professionals working in fields of human and medical genetics. Each issue is guest edited by a researcher in a featured area of genetics, offering a collection of thematic reviews from specialists around the world. Seminars in Medical Genetics publishes four times per year.
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