Yasunori Yamada, Masatomo Kobayashi, Kaoru Shinkawa, M. Nemoto, Miho Ota, K. Nemoto, T. Arai
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引用次数: 2
摘要
痴呆症的早期诊断,特别是在前驱阶段(即轻度认知障碍,或MCI),已成为研究和临床重点,但仍然具有挑战性。绘图过程的自动分析已被研究为一种有前途的筛查前驱和临床痴呆的手段,提供多方面的信息,包括特征,如绘图速度,笔的姿势,书写压力和停顿。我们研究了使用这些特征的可行性,不仅用于检测前驱和临床痴呆,还用于预测使用迷你精神状态检查(MMSE)评估的认知障碍的严重程度,以及通过内侧颞叶(MTL)萎缩评估的神经病理改变的严重程度。我们用数字化平板和笔收集了145名认知正常(CN)、轻度认知障碍(MCI)和痴呆老年人的绘画数据。嵌套交叉验证结果表明,结合绘图特征可用于CN、MCI和痴呆的分类,AUC为0.909,准确率为75.1% (CN vs MCI: 82.4%;CN与痴呆:准确率为92.2%;MCI与痴呆:准确率为80.3%),预测MMSE评分的R2为0.491,MTL萎缩严重程度的R2为0.293。我们的研究结果表明,绘制过程的自动化分析可以提供有关痴呆症引起的认知障碍和神经病理变化的信息,这有助于识别前驱和临床痴呆症作为数字生物标志物。
Automated Analysis of Drawing Process for Detecting Prodromal and Clinical Dementia
Early diagnosis of dementia, particularly in the prodromal stage (i.e., mild cognitive impairment, or MCI), has become a research and clinical priority but remains challenging. Automated analysis of the drawing process has been studied as a promising means for screening prodromal and clinical dementia, providing multifaceted information encompassing features, such as drawing speed, pen posture, writing pressure, and pauses. We examined the feasibility of using these features not only for detecting prodromal and clinical dementia but also for predicting the severity of cognitive impairments assessed using Mini-Mental State Examination (MMSE) as well as the severity of neuropathological changes assessed by medial temporal lobe (MTL) atrophy. We collected drawing data with a digitizing tablet and pen from 145 older adults of cognitively normal (CN), MCI, and dementia. The nested cross-validation results indicate that the combination of drawing features could be used to classify CN, MCI, and dementia with an AUC of 0.909 and 75.1% accuracy (CN vs. MCI: 82.4% accuracy; CN vs. dementia: 92.2% accuracy; MCI vs. dementia: 80.3% accuracy) and predict MMSE scores with an $R2$ of 0.491 and severity of MTL atrophy with an $R2$ of 0.293. Our findings suggest that automated analysis of the drawing process can provide information about cognitive impairments and neuropathological changes due to dementia, which can help identify prodromal and clinical dementia as a digital biomarker.