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利用非负矩阵分解从电子健康记录中学习多重疾病模式。

Learning multimorbidity patterns from electronic health records using Non-negative Matrix Factorisation.

机构信息

Deep Medicine, Oxford Martin School, University of Oxford, Oxford, United Kingdom; NIHR Oxford Biomedical Research Centre, Oxford University Hospitals NHS Foundation Trust, Oxford, United Kingdom.

Deep Medicine, Oxford Martin School, University of Oxford, Oxford, United Kingdom.

出版信息

J Biomed Inform. 2020 Dec;112:103606. doi: 10.1016/j.jbi.2020.103606. Epub 2020 Oct 27.

Abstract

Multimorbidity, or the presence of several medical conditions in the same individual, has been increasing in the population - both in absolute and relative terms. Nevertheless, multimorbidity remains poorly understood, and the evidence from existing research to describe its burden, determinants and consequences has been limited. Previous studies attempting to understand multimorbidity patterns are often cross-sectional and do not explicitly account for multimorbidity patterns' evolution over time; some of them are based on small datasets and/or use arbitrary and narrow age ranges; and those that employed advanced models, usually lack appropriate benchmarking and validations. In this study, we (1) introduce a novel approach for using Non-negative Matrix Factorisation (NMF) for temporal phenotyping (i.e., simultaneously mining disease clusters and their trajectories); (2) provide quantitative metrics for the evaluation of these clusters and trajectories; and (3) demonstrate how the temporal characteristics of the disease clusters that result from our model can help mine multimorbidity networks and generate new hypotheses for the emergence of various multimorbidity patterns over time. We trained and evaluated our models on one of the world's largest electronic health records (EHR) datasets, containing more than 7 million patients, from which over 2 million where relevant to, and hence included in this study.

摘要

多发病,即同一患者存在多种疾病,在人群中呈绝对和相对增长趋势。然而,多发病仍未被充分了解,现有研究对其负担、决定因素和后果的证据有限。之前尝试理解多发病模式的研究往往是横断面的,没有明确考虑多发病模式随时间的演变;其中一些基于小数据集和/或使用任意和狭窄的年龄范围;而那些使用先进模型的研究,通常缺乏适当的基准测试和验证。在这项研究中,我们 (1) 介绍了一种新颖的方法,用于使用非负矩阵分解 (NMF) 进行时间表型分析(即同时挖掘疾病群集及其轨迹);(2) 提供了评估这些群集和轨迹的定量指标;(3) 展示了我们模型产生的疾病群集的时间特征如何有助于挖掘多发病网络,并生成随时间出现各种多发病模式的新假设。我们在一个世界上最大的电子健康记录 (EHR) 数据集之一上训练和评估了我们的模型,该数据集包含超过 700 万患者,其中超过 200 万与本研究相关并包含在本研究中。

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