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Modeling Nonhomogeneous Markov Processes via Time Transformation

Author

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  • R. A. Hubbard
  • L. Y. T. Inoue
  • J. R. Fann

Abstract

Summary Longitudinal studies are a powerful tool for characterizing the course of chronic disease. These studies are usually carried out with subjects observed at periodic visits giving rise to panel data. Under this observation scheme the exact times of disease state transitions and sequence of disease states visited are unknown and Markov process models are often used to describe disease progression. Most applications of Markov process models rely on the assumption of time homogeneity, that is, that the transition rates are constant over time. This assumption is not satisfied when transition rates depend on time from the process origin. However, limited statistical tools are available for dealing with nonhomogeneity. We propose models in which the time scale of a nonhomogeneous Markov process is transformed to an operational time scale on which the process is homogeneous. We develop a method for jointly estimating the time transformation and the transition intensity matrix for the time transformed homogeneous process. We assess maximum likelihood estimation using the Fisher scoring algorithm via simulation studies and compare performance of our method to homogeneous and piecewise homogeneous models. We apply our methodology to a study of delirium progression in a cohort of stem cell transplantation recipients and show that our method identifies temporal trends in delirium incidence and recovery.

Suggested Citation

  • R. A. Hubbard & L. Y. T. Inoue & J. R. Fann, 2008. "Modeling Nonhomogeneous Markov Processes via Time Transformation," Biometrics, The International Biometric Society, vol. 64(3), pages 843-850, September.
  • Handle: RePEc:bla:biomet:v:64:y:2008:i:3:p:843-850
    DOI: 10.1111/j.1541-0420.2007.00932.x
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    References listed on IDEAS

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    1. Chantal Guihenneuc-Jouyaux & Sylvia Richardson & Ira M. Longini Jr., 2000. "Modeling Markers of Disease Progression by a Hidden Markov Process: Application to Characterizing CD4 Cell Decline," Biometrics, The International Biometric Society, vol. 56(3), pages 733-741, September.
    2. Rafael Pérez‐Ocón & Juan Eloy Ruiz‐Castro & M. Luz Gámiz‐Pérez, 2001. "Non‐homogeneous Markov models in the analysis of survival after breast cancer," Journal of the Royal Statistical Society Series C, Royal Statistical Society, vol. 50(1), pages 111-124.
    3. Mogens Bladt & Michael Sørensen, 2005. "Statistical inference for discretely observed Markov jump processes," Journal of the Royal Statistical Society Series B, Royal Statistical Society, vol. 67(3), pages 395-410, June.
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    Citations

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    Cited by:

    1. Jane M. Lange & Rebecca A. Hubbard & Lurdes Y. T. Inoue & Vladimir N. Minin, 2015. "A joint model for multistate disease processes and random informative observation times, with applications to electronic medical records data," Biometrics, The International Biometric Society, vol. 71(1), pages 90-101, March.
    2. Andrew C. Titman, 2011. "Flexible Nonhomogeneous Markov Models for Panel Observed Data," Biometrics, The International Biometric Society, vol. 67(3), pages 780-787, September.
    3. Chen, Baojiang & Zhou, Xiao-Hua, 2013. "A correlated random effects model for non-homogeneous Markov processes with nonignorable missingness," Journal of Multivariate Analysis, Elsevier, vol. 117(C), pages 1-13.
    4. Daewoo Pak & Jing Ning & Richard J. Kryscio & Yu Shen, 2023. "Evaluation of the natural history of disease by combining incident and prevalent cohorts: application to the Nun Study," Lifetime Data Analysis: An International Journal Devoted to Statistical Methods and Applications for Time-to-Event Data, Springer, vol. 29(4), pages 752-768, October.
    5. repec:jss:jstsof:38:i08 is not listed on IDEAS

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