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.

IF 4.1 2区 医学 Q1 CLINICAL NEUROLOGY
I-Chun Chen, Che-Lun Chang, Meng-Han Chang, Li-Wei Ko
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引用次数: 0

Abstract

Background: A multi-method, multi-informant approach is crucial for evaluating attention-deficit/hyperactivity disorders (ADHD) in preschool children due to the diagnostic complexities and challenges at this developmental stage. However, most artificial intelligence (AI) studies on the automated detection of ADHD have relied on using a single datatype. This study aims to develop a reliable multimodal AI-detection system to facilitate the diagnosis of ADHD in young children.

Methods: 78 young children were recruited, including 43 diagnosed with ADHD (mean age: 68.07 ± 6.19 months) and 35 with typical development (mean age: 67.40 ± 5.44 months). Machine learning and deep learning methods were adopted to develop three individual predictive models using electroencephalography (EEG) data recorded with a wearable wireless device, scores from the computerized attention assessment via Conners' Kiddie Continuous Performance Test Second Edition (K-CPT-2), and ratings from ADHD-related symptom scales. Finally, these models were combined to form a single ensemble model.

Results: The ensemble model achieved an accuracy of 0.974. While individual modality provided the optimal classification with an accuracy rate of 0.909, 0.922, and 0.950 using the ADHD-related symptom rating scale, the K-CPT-2 score, and the EEG measure, respectively. Moreover, the findings suggest that teacher ratings, K-CPT-2 reaction time, and occipital high-frequency EEG band power values are significant features in identifying young children with ADHD.

Conclusions: This study addresses three common issues in ADHD-related AI research: the utility of wearable technologies, integrating databases from diverse ADHD diagnostic instruments, and appropriately interpreting the models. This established multimodal system is potentially reliable and practical for distinguishing ADHD from TD, thus further facilitating the clinical diagnosis of ADHD in preschool young children.

将可穿戴脑电图与行为测量相结合,建立一个实用的多领域模型,以帮助诊断患有注意力缺陷/多动障碍的幼儿。
背景:学龄前儿童的注意力缺陷/多动症(ADHD)诊断复杂且具有挑战性,因此采用多方法、多信息的方法对评估学龄前儿童的注意力缺陷/多动症至关重要。然而,大多数关于自动检测多动症的人工智能(AI)研究都依赖于使用单一数据类型。本研究旨在开发一种可靠的多模态人工智能检测系统,以促进幼儿多动症的诊断。方法:招募 78 名幼儿,包括 43 名确诊为多动症的幼儿(平均年龄:68.07 ± 6.19 个月)和 35 名发育典型的幼儿(平均年龄:67.40 ± 5.44 个月)。研究人员采用机器学习和深度学习方法,利用可穿戴无线设备记录的脑电图(EEG)数据、通过康纳斯儿童连续表现测试第二版(K-CPT-2)进行的计算机化注意力评估得分以及多动症相关症状量表的评分,开发了三个单独的预测模型。最后,这些模型被组合成一个单一的集合模型:结果:组合模型的准确率达到了 0.974。而使用 ADHD 相关症状评分量表、K-CPT-2 评分和脑电图测量,单个模式提供了最佳分类,准确率分别为 0.909、0.922 和 0.950。此外,研究结果表明,教师评分、K-CPT-2 反应时间和枕部高频脑电图波段功率值是识别多动症幼儿的重要特征:本研究解决了与多动症相关的人工智能研究中的三个常见问题:可穿戴技术的实用性、整合来自不同多动症诊断工具的数据库以及适当解释模型。这个已建立的多模态系统在区分多动症和TD方面具有潜在的可靠性和实用性,从而进一步促进了学龄前幼儿多动症的临床诊断。
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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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