Division of Epidemiology and Biostatistics, School of Public Health, University of Illinois at Chicago, Chicago, Illinois, USA.
Stat Med. 2023 Feb 10;42(3):316-330. doi: 10.1002/sim.9619. Epub 2022 Nov 28.
The shared random effects joint model is one of the most widely used approaches to study the associations between longitudinal biomarkers and a survival outcome and make dynamic risk predictions using the longitudinally measured biomarkers. Various types of joint models have been developed under different settings in the past decades. One major limitation of joint models is that they could be computationally expensive for complex models where the number of the shared random effects is large. Moreover, the inferential accuracy of joint models could also be diminished for complex models due to approximation errors. However, complex models are frequently needed in practice, for example, when the longitudinal biomarkers have nonlinear trajectories over time or the number of longitudinal biomarkers of interest is large. In this article, we propose a novel Gaussian variational approximate inference approach for fitting joint models, which significantly improves computational efficiency while maintaining inferential accuracy. We conduct extensive simulation studies to evaluate the performance of our proposed method and compare it to existing methods. The performance of our proposed method is further demonstrated on a dataset of patients with primary biliary cirrhosis.
共享随机效应联合模型是研究纵向生物标志物与生存结局之间关联并使用纵向测量生物标志物进行动态风险预测的最广泛使用的方法之一。在过去几十年中,已经在不同的设置下开发了各种类型的联合模型。联合模型的一个主要局限性是,对于共享随机效应数量较大的复杂模型,计算成本可能很高。此外,由于近似误差,复杂模型的联合模型推断准确性也可能降低。然而,在实践中经常需要复杂的模型,例如,当纵向生物标志物随时间具有非线性轨迹或感兴趣的纵向生物标志物数量较大时。本文提出了一种新的用于拟合联合模型的高斯变分近似推理方法,该方法在保持推断准确性的同时,显著提高了计算效率。我们进行了广泛的模拟研究来评估我们提出的方法的性能,并将其与现有方法进行比较。我们提出的方法的性能在原发性胆汁性肝硬化患者数据集上进一步得到了验证。