Shah Jay, Krell-Roesch Janina, Forzani Erica, Knopman David S, Jack Cliff R, Petersen Ronald C, Che Yiming, Wu Teresa, Geda Yonas E
School of Computing and Augmented Intelligence, Arizona State University, Tempe, AZ, USA.
ASU-Mayo Center for Innovative Imaging, Tempe, AZ, USA.
J Alzheimers Dis. 2025 Feb;103(3):833-843. doi: 10.1177/13872877241306654. Epub 2025 Jan 10.
The aim of this study was to examine the potential added value of including neuropsychiatric symptoms (NPS) in machine learning (ML) models, along with demographic features and Alzheimer's disease (AD) biomarkers, to predict decline or non-decline in global and domain-specific cognitive scores among community-dwelling older adults.
To evaluate the impact of adding NPS to AD biomarkers on ML model accuracy in predicting cognitive decline among older adults.
The study was conducted in the setting of the Mayo Clinic Study of Aging, including participants aged ≥ 50 years with information on demographics (i.e., age, sex, education), NPS (i.e., Neuropsychiatric Inventory Questionnaire; Beck Depression and Anxiety Inventories), at least one AD biomarker (i.e., plasma-, neuroimaging- and/or cerebrospinal fluid [CSF]-derived), and at least 2 repeated neuropsychological assessments. We trained and tested ML models using a stepwise feature addition approach to predict decline versus non-decline in global and domain-specific (i.e., memory, language, visuospatial, and attention/executive function) cognitive scores.
ML models had better performance when NPS were included along with a) neuroimaging biomarkers for predicting decline in global cognition, as well as language and visuospatial skills; b) plasma-derived biomarkers for predicting decline in visuospatial skills; and c) CSF-derived biomarkers for predicting decline in attention/executive function, language, and memory.
NPS, added to ML models including demographic and AD biomarker data, improves prediction of downward trajectories in global and domain-specific cognitive scores among community-dwelling older adults, albeit effect sizes are small. These preliminary findings need to be confirmed by future cohort studies.
本研究的目的是检验在机器学习(ML)模型中纳入神经精神症状(NPS)以及人口统计学特征和阿尔茨海默病(AD)生物标志物,以预测社区居住的老年人在整体和特定领域认知评分方面下降或未下降的潜在附加价值。
评估在AD生物标志物中加入NPS对ML模型预测老年人认知下降准确性的影响。
该研究在梅奥诊所衰老研究的背景下进行,纳入年龄≥50岁的参与者,他们有关于人口统计学(即年龄、性别、教育程度)、NPS(即神经精神问卷;贝克抑郁和焦虑量表)、至少一种AD生物标志物(即血浆、神经影像学和/或脑脊液[CSF]来源的)以及至少2次重复神经心理学评估的信息。我们使用逐步特征添加方法训练和测试ML模型,以预测整体和特定领域(即记忆、语言、视觉空间和注意力/执行功能)认知评分的下降与未下降情况。
当NPS与以下生物标志物一起纳入时,ML模型表现更好:a)用于预测整体认知、语言和视觉空间技能下降的神经影像学生物标志物;b)用于预测视觉空间技能下降的血浆来源生物标志物;c)用于预测注意力/执行功能、语言和记忆下降的脑脊液来源生物标志物。
在包含人口统计学和AD生物标志物数据的ML模型中加入NPS,可改善对社区居住老年人整体和特定领域认知评分下降轨迹的预测,尽管效应大小较小。这些初步发现需要未来的队列研究加以证实。