Department of Clinical Neurosciences, University of Calgary, 2500 University Drive NW, Calgary, AB, T2N 1N4, Canada.
Hotchkiss Brain Institute, Cumming School of Medicine, University of Calgary, 3330 Hospital Dr NW, Calgary, AB, T2N 4N1, Canada.
Sci Rep. 2023 Aug 14;13(1):13193. doi: 10.1038/s41598-023-37644-6.
Patients with Parkinson's Disease (PD) often suffer from cognitive decline. Accurate prediction of cognitive decline is essential for early treatment of at-risk patients. The aim of this study was to develop and evaluate a multimodal machine learning model for the prediction of continuous cognitive decline in patients with early PD. We included 213 PD patients from the Parkinson's Progression Markers Initiative (PPMI) database. Machine learning was used to predict change in Montreal Cognitive Assessment (MoCA) score using the difference between baseline and 4-years follow-up data as outcome. Input features were categorized into four sets: clinical test scores, cerebrospinal fluid (CSF) biomarkers, brain volumes, and genetic variants. All combinations of input feature sets were added to a basic model, which consisted of demographics and baseline cognition. An iterative scheme using RReliefF-based feature ranking and support vector regression in combination with tenfold cross validation was used to determine the optimal number of predictive features and to evaluate model performance for each combination of input feature sets. Our best performing model consisted of a combination of the basic model, clinical test scores and CSF-based biomarkers. This model had 12 features, which included baseline cognition, CSF phosphorylated tau, CSF total tau, CSF amyloid-beta, geriatric depression scale (GDS) scores, and anxiety scores. Interestingly, many of the predictive features in our model have previously been associated with Alzheimer's disease, showing the importance of assessing Alzheimer's disease pathology in patients with Parkinson's disease.
帕金森病(PD)患者常伴有认知能力下降。准确预测认知能力下降对于高危患者的早期治疗至关重要。本研究旨在开发和评估一种多模态机器学习模型,用于预测早期 PD 患者的连续认知能力下降。我们纳入了帕金森进展标志物倡议(PPMI)数据库中的 213 名 PD 患者。机器学习用于预测蒙特利尔认知评估(MoCA)评分的变化,以基线和 4 年随访数据之间的差异作为结果。输入特征分为四组:临床测试评分、脑脊液(CSF)生物标志物、脑容量和遗传变异。将输入特征集的所有组合添加到基本模型中,该模型由人口统计学和基线认知组成。使用基于 RReliefF 的特征排序和支持向量回归结合十折交叉验证的迭代方案,确定最佳预测特征数量,并评估每种输入特征集组合的模型性能。我们表现最佳的模型由基本模型、临床测试评分和基于 CSF 的生物标志物组成。该模型有 12 个特征,包括基线认知、CSF 磷酸化 tau、CSF 总 tau、CSF 淀粉样蛋白-β、老年抑郁量表(GDS)评分和焦虑评分。有趣的是,我们模型中的许多预测特征以前与阿尔茨海默病有关,这表明在帕金森病患者中评估阿尔茨海默病病理的重要性。