Modeling comorbidity of chronic diseases using coupled hidden Markov model with bivariate discrete copula

Zarina Oflaz1, Ceylan Yozgatligil2, A Sevtap Selcuk-Kestel3

  • 1Department of Industrial Engineering, KTO Karatay University, Konya, Turkey.

Insights

This study models interacting chronic diseases using a coupled hidden Markov model. The approach effectively captures disease comorbidity dynamics from population data, even without clinical information.

Area of Science:

  • Biostatistics
  • Epidemiology
  • Computational Biology

Background:

  • Chronic diseases often interact and share risk factors, a phenomenon known as comorbidity.
  • Comorbidity is crucial for accurate actuarial valuations and understanding disease progression.
  • Existing models may not fully capture the complex dynamics of interacting chronic conditions.

Purpose of the Study:

  • To develop a novel statistical model for analyzing parallel, interacting chronic disease processes.
  • To introduce a coupled hidden Markov model (CHMM) integrated with bivariate discrete copula functions.
  • To provide a method for estimating model parameters and addressing computational challenges.

Main Methods:

  • Utilized a combination of hidden Markov theory and copula functions to model disease interactions.
  • Developed a CHMM with a bivariate discrete copula within the hidden process.
  • Employed a variational expectation-maximization (VEM) algorithm for parameter estimation.
  • Addressed numerical underflow issues in forward-backward probability computations.

Main Results:

  • Simulation studies demonstrated satisfactory performance of the proposed CHMM across different association levels.
  • The model successfully defined the dependency structure and dynamics of unobserved disease data.
  • Application to hospital appointment data showed the model's utility in analyzing comorbidity.

Conclusions:

  • The proposed CHMM offers a robust framework for investigating disease comorbidity.
  • The model is particularly valuable when analyzing population dynamics over time without access to clinical data.
  • This approach enhances our understanding of complex disease interactions and their impact.

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