Kim Seongho, Jang Hyejeong, Wu Dongfeng, Abrams Judith
Biostatistics Core, Karmanos Cancer Institute, Department of Oncology, Wayne State University School of Medicine, Detroit, MI 48201.
Department of Bioinformatics and Biostatistics, School of Public Health and Information Sciences, University of Louisville, Louisville, KY 40202.
J Biom Biostat. 2015 Dec;6(5). doi: 10.4172/2155-6180.1000271. Epub 2015 Dec 30.
A nonlinear mixed-effects approach is developed for disease progression models that incorporate variation in age in a Bayesian framework. We further generalize the probability model for sensitivity to depend on age at diagnosis, time spent in the preclinical state and sojourn time. The developed models are then applied to the Johns Hopkins Lung Project data and the Health Insurance Plan for Greater New York data using Bayesian Markov chain Monte Carlo and are compared with the estimation method that does not consider random-effects from age. Using the developed models, we obtain not only age-specific individual-level distributions, but also population-level distributions of sensitivity, sojourn time and transition probability.
在贝叶斯框架下,我们针对纳入年龄差异的疾病进展模型开发了一种非线性混合效应方法。我们进一步推广了敏感性概率模型,使其依赖于诊断时的年龄、临床前状态所花费的时间以及停留时间。然后,使用贝叶斯马尔可夫链蒙特卡罗方法将所开发的模型应用于约翰霍普金斯肺部项目数据和大纽约地区健康保险计划数据,并与不考虑年龄随机效应的估计方法进行比较。使用所开发的模型,我们不仅获得了特定年龄的个体水平分布,还得到了敏感性、停留时间和转移概率的总体水平分布。