Fitting and interpreting continuous-time latent Markov models for panel data

被引:16
|
作者
Lange, Jane M. [1 ]
Minin, Vladimir N. [2 ]
机构
[1] Univ Washington, Dept Biostat, Seattle, WA 98195 USA
[2] Univ Washington, Dept Stat, Seattle, WA 98195 USA
基金
美国国家科学基金会;
关键词
disease process; EM algorithm; multistate model; panel data; phase-type; BRONCHIOLITIS-OBLITERANS-SYNDROME; PHASE-TYPE DISTRIBUTIONS; OBSERVED INFORMATION MATRIX; STATISTICAL-INFERENCE; DISEASE PROGRESSION; MULTISTATE MODELS; EM; ALGORITHM; CONVERGENCE; COMPUTATION;
D O I
10.1002/sim.5861
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Multistate models characterize disease processes within an individual. Clinical studies often observe the disease status of individuals at discrete time points, making exact times of transitions between disease states unknown. Such panel data pose considerable modeling challenges. Assuming the disease process progresses accordingly, a standard continuous-time Markov chain (CTMC) yields tractable likelihoods, but the assumption of exponential sojourn time distributions is typically unrealistic. More flexible semi-Markov models permit generic sojourn distributions yet yield intractable likelihoods for panel data in the presence of reversible transitions. One attractive alternative is to assume that the disease process is characterized by an underlying latent CTMC, with multiple latent states mapping to each disease state. These models retain analytic tractability due to the CTMC framework but allow for flexible, duration-dependent disease state sojourn distributions. We have developed a robust and efficient expectation-maximization algorithm in this context. Our complete data state space consists of the observed data and the underlying latent trajectory, yielding computationally efficient expectation and maximization steps. Our algorithm outperforms alternative methods measured in terms of time to convergence and robustness. We also examine the frequentist performance of latent CTMC point and interval estimates of disease process functionals based on simulated data. The performance of estimates depends on time, functional, and data-generating scenario. Finally, we illustrate the interpretive power of latent CTMC models for describing disease processes on a dataset of lung transplant patients. We hope our work will encourage wider use of these models in the biomedical setting. Copyright (c) 2013 John Wiley & Sons, Ltd.
引用
收藏
页码:4581 / 4595
页数:15
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