Mark Cauchi, Andrew R Mills, Allan Lawrie, David G Kiely, Visakan Kadirkamanathan
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引用次数: 0
Abstract
Monitoring disease progression often involves tracking biomarker measurements over time. Joint models (JMs) for longitudinal and survival data provide a framework to explore the relationship between time-varying biomarkers and patients' event outcomes, offering the potential for personalized survival predictions. In this article, we introduce the linear state space dynamic survival model for handling longitudinal and survival data. This model enhances the traditional linear Gaussian state space model by including survival data. It differs from the conventional JMs by offering an alternative interpretation via differential or difference equations, eliminating the need for creating a design matrix. To showcase the model's effectiveness, we conduct a simulation case study, emphasizing its performance under conditions of limited observed measurements. We also apply the proposed model to a dataset of pulmonary arterial hypertension patients, demonstrating its potential for enhanced survival predictions when compared with conventional risk scores.
监测疾病进展通常需要跟踪生物标志物随时间变化的测量结果。纵向数据和生存数据的联合模型(JMs)为探索时变生物标志物与患者事件结果之间的关系提供了一个框架,为个性化生存预测提供了可能性。本文介绍了处理纵向和生存数据的线性状态空间动态生存模型。该模型包含了生存数据,从而增强了传统的线性高斯状态空间模型。它与传统的 JM 不同,通过微分方程或差分方程提供了另一种解释,无需创建设计矩阵。为了展示该模型的有效性,我们进行了一项模拟案例研究,强调其在有限观测测量条件下的性能。我们还将提出的模型应用于肺动脉高压患者的数据集,证明与传统风险评分相比,该模型具有提高生存预测的潜力。
期刊介绍:
J. R. Soc. Interface welcomes articles of high quality research at the interface of the physical and life sciences. It provides a high-quality forum to publish rapidly and interact across this boundary in two main ways: J. R. Soc. Interface publishes research applying chemistry, engineering, materials science, mathematics and physics to the biological and medical sciences; it also highlights discoveries in the life sciences of relevance to the physical sciences. Both sides of the interface are considered equally and it is one of the only journals to cover this exciting new territory. J. R. Soc. Interface welcomes contributions on a diverse range of topics, including but not limited to; biocomplexity, bioengineering, bioinformatics, biomaterials, biomechanics, bionanoscience, biophysics, chemical biology, computer science (as applied to the life sciences), medical physics, synthetic biology, systems biology, theoretical biology and tissue engineering.