Developing multifactorial dementia prediction models using clinical variables from cohorts in the US and Australia

Caitlin A Finney, David A Brown, Artur Shvetcov, Alzheimers Disease Neuroimaging Initiative, Australian Imaging Biomarkers and Lifestyle Flagship Study of Ageing
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Abstract

INTRODUCTION Existing dementia prediction models using non-neuroimaging clinical measures have been limited in their ability to identify disease. This study used machine learning to re-examine the diagnostic potential of clinical measures for dementia. METHODS Data was sourced from the Australian Imaging, Biomarkers, and Lifestyle Flagship Study of Ageing (AIBL) and the Alzheimers Disease Neuroimaging Initiative (ADNI). Clinical variables included 21 measures across medical history, hematological and other blood tests, and APOE genotype. Tree-based machine learning algorithms and artificial neural networks were used. RESULTS APOE genotype was the best predictor of dementia cases and healthy controls. Our results, however, demonstrated that there are limitations when using publicly accessible cohort data that may limit the generalizability and interpretability of such predictive models. DISCUSSION Future research should examine the use of routine APOE genetic testing for dementia diagnostics. It should also focus on clearly unifying data across clinical cohorts.
利用美国和澳大利亚队列中的临床变量开发多因素痴呆症预测模型
引言 现有的痴呆症预测模型使用非神经影像学临床测量方法,但其识别疾病的能力有限。本研究利用机器学习重新检验了痴呆症临床指标的诊断潜力。方法数据来源于澳大利亚老龄化成像、生物标记和生活方式旗舰研究(AIBL)和阿尔茨海默病神经成像倡议(ADNI)。临床变量包括病史、血液学和其他血液检查以及 APOE 基因型等 21 项指标。使用了基于树的机器学习算法和人工神经网络。结果APOE基因型是痴呆症病例和健康对照组的最佳预测指标。然而,我们的研究结果表明,使用可公开获取的队列数据存在局限性,可能会限制此类预测模型的推广性和可解释性。未来的研究还应该关注临床队列数据的明确统一。
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