使用手动运动测量对轻度认知障碍和阿尔茨海默病进行分类。
Classification of Mild Cognitive Impairment and Alzheimer's Disease Using Manual Motor Measures.
机构信息
Department of Psychiatry, University of Utah, Salt Lake City, Utah, USA.
Huntsman Mental Health Institute, University of Utah, Salt Lake City, Utah, USA.
出版信息
Neurodegener Dis. 2024;24(2):54-70. doi: 10.1159/000539800. Epub 2024 Jun 12.
INTRODUCTION
Manual motor problems have been reported in mild cognitive impairment (MCI) and Alzheimer's disease (AD), but the specific aspects that are affected, their neuropathology, and potential value for classification modeling is unknown. The current study examined if multiple measures of motor strength, dexterity, and speed are affected in MCI and AD, related to AD biomarkers, and are able to classify MCI or AD.
METHODS
Fifty-three cognitively normal (CN), 33 amnestic MCI, and 28 AD subjects completed five manual motor measures: grip force, Trail Making Test A, spiral tracing, finger tapping, and a simulated feeding task. Analyses included (1) group differences in manual performance; (2) associations between manual function and AD biomarkers (PET amyloid β, hippocampal volume, and APOE ε4 alleles); and (3) group classification accuracy of manual motor function using machine learning.
RESULTS
Amnestic MCI and AD subjects exhibited slower psychomotor speed and AD subjects had weaker dominant hand grip strength than CN subjects. Performance on these measures was related to amyloid β deposition (both) and hippocampal volume (psychomotor speed only). Support vector classification well-discriminated control and AD subjects (area under the curve of 0.73 and 0.77, respectively) but poorly discriminated MCI from controls or AD.
CONCLUSION
Grip strength and spiral tracing appear preserved, while psychomotor speed is affected in amnestic MCI and AD. The association of motor performance with amyloid β deposition and atrophy could indicate that this is due to amyloid deposition in and atrophy of motor brain regions, which generally occurs later in the disease process. The promising discriminatory abilities of manual motor measures for AD emphasize their value alongside other cognitive and motor assessment outcomes in classification and prediction models, as well as potential enrichment of outcome variables in AD clinical trials.
简介
在轻度认知障碍(MCI)和阿尔茨海默病(AD)中已经报道了手动运动问题,但具体受影响的方面、它们的神经病理学以及分类建模的潜在价值尚不清楚。本研究检查了 MCI 和 AD 中是否存在多种运动力量、灵活性和速度的测量值受到影响,以及它们与 AD 生物标志物的关系,以及是否能够对 MCI 或 AD 进行分类。
方法
53 名认知正常(CN)、33 名遗忘型 MCI 和 28 名 AD 受试者完成了五项手动运动测量:握力、连线测试 A、螺旋描记、手指敲击和模拟进食任务。分析包括:(1)手动表现的组间差异;(2)手动功能与 AD 生物标志物(PET 淀粉样蛋白 β、海马体积和 APOE ε4 等位基因)之间的关联;(3)使用机器学习对手动运动功能进行组分类准确性。
结果
遗忘型 MCI 和 AD 受试者表现出较慢的心理运动速度,而 AD 受试者的优势手握力比 CN 受试者弱。这些测量值的表现与淀粉样蛋白 β 沉积(均)和海马体积(心理运动速度仅)有关。支持向量分类器很好地区分了对照组和 AD 组(曲线下面积分别为 0.73 和 0.77),但区分 MCI 与对照组或 AD 的能力较差。
结论
握力和螺旋描记似乎保持不变,而心理运动速度在遗忘型 MCI 和 AD 中受到影响。运动表现与淀粉样蛋白 β 沉积和萎缩的关联表明,这是由于运动脑区的淀粉样蛋白沉积和萎缩所致,这通常发生在疾病过程的后期。手动运动测量对 AD 的有希望的区分能力强调了它们在分类和预测模型中与其他认知和运动评估结果一起的价值,以及在 AD 临床试验中对结果变量的潜在富集。